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Novel Role of the SIRT1 in Endocrine and Metabolic Diseases
Chenxi Lu, Huadong Zhao, Yanqing Liu and 9 more
International Journal of Biological Sciences · 2023 · Review
Abstract
-dependent deacetylase, is a cellular regulator that has received extensive attention in recent years and regarded as a sensor of cellular energy and metabolism. The accumulated evidence suggests that SIRT1 is involved in the development of endocrine and metabolic diseases. In a variety of organisms, SIRT1 regulates gene expression through the deacetylation of histone, transcription factors, and lysine residues of other modified proteins including several metabolic and endocrine signal transcription factors, thereby enhancing the therapeutic effects of endocrine and metabolic diseases. These evidences indicate that targeting SIRT1 has promising applications in the treatment of endocrine and metabolic diseases. This review focuses on the role of SIRT1 in endocrine and metabolic diseases. First, we describe the background and structure of SIRT1. Then, we outline the role of SIRT1 in endocrine and metabolic diseases such as hyperuricemia, diabetes, hypertension, hyperlipidemia, osteoporosis, and polycystic ovarian syndrome. Subsequently, the SIRT1 agonists and inhibitors in the above diseases are summarized and future research directions are proposed. Overall, the information presents here may highlight the potential of SIRT1 as a future biomarker and therapeutic target for endocrine and metabolic diseases.
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From PubMed Central, U.S. National Library of Medicine, as current on Oct 25, 2026. Paragraph numbers are ours, so an answer can point at one.
Introduction
SIRT1 is a nicotinamide adenine dinucleotide (NAD+)-dependent deacetylase, which deacetylates histone and non-histone proteins and is involved in the regulation of many physiological functions, including endocrine, metabolic regulation, immune response, oxidative stress, inflammation, and ageing -. As a key regulator of energy, SIRT1 affects glucose and lipid metabolism by stimulating endocrine signaling, which is associated with many molecules related to glucose/lipid metabolism, such as Adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK), Forkhead box O3 (FOXO3), Glucose Transporter 4 (GLUT4), Peroxisome proliferators-activated receptor γ (PPARγ), and Proliferator-activated receptor-gamma co-activator-1α (PGC-1α) -. The activation of SIRT1 have been reported to improve insulin secretion. In contrast, SIRT1 deficiency leads to the decrease in the secretion of thyroid hormone, estrogen, testosterone, and pituitary hormone, causing disorders of endocrine and metabolic system, thereby developing into obesity, diabetes, hyperuricemia, hyperlipidemia, hypertension. According to current research on SIRT1, this review focuses on the role of SIRT1 in endocrine and metabolic diseases. First, we sketch out the background and structure of SIRT1. Then, we highlight the relationship between SIRT1 and endocrine and metabolic diseases. Subsequently, we summarize the agonists/inhibitors of SIRT1 in endocrine and metabolic diseases. Finally, we propose future research directions between SIRT1 and endocrine and metabolic diseases. Although mature researches have been appeared on SIRT1, it is still an attractive node in the field of endocrine and metabolic diseases and provides new target for the treatment of the above diseases.
Sirtuins is also known as silent information regulator 2 (Sir2),. Increasing the dosage or activity of Sir2 has been shown to extend the life spans of yeast, worms, and flies, while deletions or mutations of the Sir2 reverses the result,,. Sirtuins family consists of 7 members (SIRT1-SIRT7), which can be divided into four categories according to their structural similarity. SIRT1, SIRT2 and SIRT3 belong to type Ⅰ, SIRT4 belongs to type Ⅱ, SIRT5 belongs to type Ⅲ, as well as SIRT6 and SIRT7 belong to IVa and IVb subtypes of type IV respectively. In addition, according to their distribution, they are also divided into nuclear proteins (SIRT1, SIRT3, SIRT6 and SIRT7), plasmic proteins (SIRT2) and mitochondrial proteins (SIRT4 and SIRT5). The deacetylation activity of SIRT1 and other sirtuins need the help of NAD+, which is a cofactor also involved in DNA damage repair. Through deacetylation, the acetyl group of the acetylated protein substrate is transferred to the ADP-ribose (ADPR) of NAD+, and products such as deacetylation protein, Nicotinamide (NAM) and 2-O-acetyl-ADP-ribose,. As a classic member of Sirtuins family, SIRT1 is more conservative than other members in structure, which is of great concern.
The SIRT1 gene is located on human chromosome 10 with a total length of approximately 33 Kb and contains 9 exons, 8 introns and untranslated regions. The human SIRT1 protein is composed of 747 amino acids and mainly contains the three structures (central nuclear catalytic structural domain, nuclear localization signals (NLS), and nuclear export signals (NES)),, there into the catalytic structural domain covers the substrate binding pocket and the NAD+ binding pocket (Figure 1). The histidine at position 363 of SIRT1, in which structural activity is dependent on the NAD+/NADH ratio in the cytoplasm, is an essential motif for deacetylation activity and involved in regulating the redox state and metabolic homeostasis. SIRT1 acts as an important transcriptional regulator with lysine deacetylation on histones regulating chromatin structural stability and protein activity, thus participating in maintaining normal cellular functions. For example, the deacetylation of SIRT1 affects the transcription of FOXO family members and PGC-1α and directly regulates lipid metabolism -. SIRT1 also deacetylates lysine at position 382 of p53 protein, preventing its transcriptional activation and p53-dependent apoptosis induction. In addition to acetylation, other modifications of SIRT1, such as phosphorylation, ubiquitination, also partake in important physiological and pathophysiological functions. AMPK directly interacts with the deacetylase active domain of SIRT1 and phosphorylates Thr344 of SIRT1, which inhibits the deacetylation activity of SIRT1. Ubiquitination stabilizes proteins by covalently adding SUMO proteins to lysine residues. The Lys734of SIRT1 is modified by ubiquitin to increase the activity and stability of the protein. Due to its unique structure and function, SIRT1 has also been confirmed to play a positive role in other aspects of mammalian health. SIRT1 deficiency leads to energy imbalance, endocrine and metabolic disorders. Meanwhile, SIRT1 deficiency also promotes the occurrence of immunodeficiency, cardiovascular diseases, and aging-related diseases -. Therefore, the systematic summary and review of the role of SIRT1 in endocrine and metabolism-related cells and diseases is crucial for future research.
The role of SIRT1 in endocrine and metabolism-related cells
Endocrine and metabolic system are interrelated and influence each other. The endocrine system consists of endocrine glands, endocrine tissues, and endocrine cells, which includes beta cells, oocytes, osteoblasts, osteoclasts, and adipocytes (Figure 2).
Beta cells
Beta cells are insulin secreting cells in pancreatic islets, also known as B cells, accounting for about 60% of islet cells. Due to morphology and function, islet cells also contain alpha cells, delta cells, and pancreatic polypeptide cells. It is well known that the impairment of beta cell function leads to insulin deficiency, which increases the level of blood glucose and diabetes. In addition, pancreatic beta cell canceration promotes the generation of insulinoma, which causes symptoms of malignant hypoglycemia. The dynamic expression of SIRT1 was observed in endocrine progenitors both beta cell regeneration in neonatal rats and the second transition phase of mouse pancreas development. SIRT1 activation promotes beta cell regeneration by activating endocrine progenitor cells. Similarly, SIRT1 enhances the secretion of insulin through NAD+-dependent deacetylation, and counteracts inflammatory signals to avoid islet cell apoptosis. In addition, palmitate also decreased the expression of SIRT1 in INS-1 cells and isolated rat islets, while the result can be reversed by SIRT1. This is because SIRT1 overexpression enhances PDX1(Pancreatic and Duodenal Homeobox 1) stimulation and antagonizes FOXO1-inhibited insulin promoter activity. PDX1 is essential for the pancreas development and beta cells formation. Wang et al., found that pancreas-specific knockout of SIRT1 inhibits PDX1 expression and impairs islet development. SIRT1 mutant mice develop progressive hyperglycemia, glucose intolerance, and insulin insufficiency, which directly correlate with SIRT1 deletion. They further confirmed that SIRT1 interacts with and deacetylates FOXA2 on the promoter of the PDX1 gene, and positively regulates its transcription. The above results suggest that SIRT1 is involved in the regulation of beta cell formation and pancreatic development. Interestingly, Pinho et al., found that impairing the function of the beta cell without SIRT1 results in reduced insulin secretion, but it is not accompanied by elevated blood glucose. This may be a unique compensatory mechanism associated with decreased expression of the glucose transporter Slc2a2/Glut2 and glucagon like peptide-1 receptor as well as marked downregulation of endoplasmic reticulum.
Oocytes
Endocrine system affects the development and maturity of female reproductive system and the function of female reproductive system. Polycystic ovary syndrome (PCOS), primary ovarian insufficiency (POI), and other diseases are frequently accompanied by oocyte damage and senescence, follicular development, and atresia dysfunction,. The ovaries are the source of oocytes and many reproductive hormones, including sex steroids, which is vital for female lifelong reproductive health. Ageing or damaged oocytes show elevated levels of reactive oxygen species (ROS) and impaired mitochondrial function, accompanied by the increased number of meiotic errors, unregulated autophagy-related proteins and early apoptosis, resulting in decreased oocyte quality and abnormal hormone secretion. Notably, SIRT1 regulates key transcription factors involved in aging and longevity, and is closely related to oxidative stress and autophagy -. During the activation of pregranulosa cells (PGCs), oocytes and primordial follicles, the level of SIRT1 is memorably increased. In addition, about half of the female mice with SIRT1 deficiency in oocytes become prematurely sterile between 9-11 months of age, the reduced ability or quality of oocyte development leads to increased oxidative stress in preimplantation embryos, which inhibits cleavage divisions. In view of that, all of that originate from defiance of oocyte-SIRT1. On the contrary, the activation of SIRT1 not only partially prevents the deficient phenotypes of ageing oocytes, but also alleviates meiosis abnormalities and oxidative stress of oocytes. Autophagy degrades proteins and organelles which is degenerated and recycle their components in the cytoplasm, which is essential for the preimplantation process of early embryonic development in mammals. Moreover, melatonin attenuates meiotic defects in oocytes by activating SIRT1 and regulating autophagy. Tamura's study also confirmed that melatonin promotes the recovery of oocytes from the fallopian tube and allows normal fertilization in vitro. Further studies showed that the mRNA expression of SIRT1, light chain 3 (LC3), and telomere length are enhanced after melatonin treatment. Xu et al. showed that the significant increase of ROS during the postovulatory ageing inhibits SIRT1 expression, promotes the deacetylation of FOXO3a and inhibits Superoxide dismutase 2 (SOD2) expression, leading to the decrease in mitochondrial function and autophagy. In conclusion, these studies show that the activation of SIRT1 is essential for the development of PCOS.
Osteoblasts and osteoclasts
Bone as an endocrine organ, which contributes to physiological regulation, cognition, glucose metabolism and hormone balance. The balance between osteoblasts and osteoclasts determines the quality of bone. SIRT1 expression is reduced in cartilage and subchondral bone plate in patients with osteoarthritis. In addition, SIRT1 maintains the balance between bone formation and resorption by regulating the ratio of osteoblasts to osteoclasts. A recent study also found that resveratrol (Res), the SIRT1 agonist, significantly improved bone quality and reduced serum alkaline phosphatase and osteocalcin levels in the rats with osteoporosis. Osteocalcin is a hormone secreted by osteoblasts and has been shown to be involved in insulin secretion, insulin resistance and energy expenditure. In MC3T3-E1 cells, inflammation increase apoptosis and decrease alkaline phosphatase (ALP) activity. While overexpression of SIRT1 inhibits osteoblast apoptosis, increases ALP activity and the expression of runt-related transcription factor 2 (Runx2) and osteocalcin. It was also found that overexpression of SIRT1 protects osteoblasts against tumor necrosis factor-α (TNF-α)-induced cell injury, at least in part, by repressing NF-κB activity and genes downstream of NF-κB, including iNOS. Specifically, TNF-α promotes iNOS expression and NO production by mediating NF-κB signaling pathway, while SIRT1 overexpression can reverse these results. Notably, Runx2 is the gene that encodes for the protein involved in the osteogenic differentiation process from mesenchymal precursors. Runx2 haploinsufficiency leads to the skeletal disorder characterized by bone and dental abnormalities known as cleidocranial dysplasia. Hong et al. found that atorvastatin increases bone mass and promotes osteogenesis in ageing apolipoprotein E-deficient mice by activating SIRT1-Runx2 axis. Additionally, Res increases the formation of SIRT1 and FOXO3a complex, regulates the activity of Runx2 promoter, and promotes ossification of human MSCs. Bone morphogenetic protein 2 (BMP2) is the key factor in inducing cartilage differentiation. SIRT1 can promote the BMP2-induced cartilage differentiation of MSCs and reduce the apoptosis and decomposition of extracellular matrix under oxidative stress. Zhao et al. also highlighted that Res dose-dependently increases both ALP and endothelial nitric oxide synthases (eNOS) levels, increase ALP, Runx2 and BMP2 and stimulate bone formation. On the contrary, SIRT1defiance reduces eNOS, BMP2 and ALP. The evidences describe above suggest that SIRT1 is the key molecule which regulates osteoblast differentiation and bone homeostasis.
Adipocytes
Adipocytes are essential for regulating pathological conditions such as obesity, diabetes and metabolic syndrome. SIRT1 knockout porcine preadipocytes are reduced and apoptosis is increased. Additionally, the mice with adipocyte-selective deletion of SIRT1 are more susceptible to diet-induced insulin resistance, which is associated with the increase in the number of adipose-resident macrophages and their polarization to the pro-inflammatory M1 subtype. It has been reported that SIRT1 inhibits the transcriptional activities of PPARγ (the key factors in adipocyte differentiation) and sterol regulatory element-binding protein 1c (SREBP1c) through deacetylation, thus suppressing adipocyte differentiation, reducing fat accumulation, and promoting fat mobilization,. SIRT1 overexpression can deacetylate Lys293 and Lys268 of PAPRγ and induce white adipose tissue remodeling. However, in SIRT1 knockout mice, fatty acid mobilization of white adipocytes is disrupted after fasting, and SIRT1 also significantly inhibits PPARγ in adipocytes. Repression of PPAR-γ by SIRT1 is also evident in adipocytes, where overexpression of SIRT1 attenuates adipogenesis, and RNA interference of SIRT1 enhances it. FOXO1 can be localized to the nuclear, cytoplasmic and mitochondrial compartments of adipocytes, affecting the source of ROS. The level of FOXO1 is decreased in adipocytes of db/db mice. Res can transport FOXO1 to the nucleus by activating SIRT1 and increase the level of FOXO1 in adipocytes. In addition, SIRT1 controls acetylation status and functional activity of FOXO1 that directly binds to the adipose triglyceride lipase (ATGL) promoter and regulates the transcription of ATGL gene, reducing the expression of AMPK in adipocytes Activated SIRT1 reduces phosphorylated-FOXO1 expression, thereby activating FOXO1 and inhibiting adipogenesis of adipocytes. Taken together, the above results indicate that SIRT1 is a novel adipocyte regulator that is associated with multiple signaling pathways such as PPARγ and FOXO1 to regulate adipocyte differentiation, fat accumulation and energy metabolism.
The role of the SIRT1 in endocrine and metabolic diseases
Under pathological conditions, endocrine disorders lead to abnormal function of endocrine glands, and then endocrine and metabolic diseases. SIRT1 in mammals can regulate the expression of target genes through various modifications, and plays an important role in endocrine and metabolic diseases,.
Hyperuricemia
Uric acid is a metabolite of purine, and it can increase and eventually lead to gout/hyperuricemia when there is a disorder of purine metabolism or uric acid excretion. Hyperuricemia is a common endocrine and metabolic disease in middle-aged and elderly men, which has seriously harmed human health. The traditional Chinese herb Smilax china L (effective component Res) has been used to treat hyperuricemia, gout and related kidney diseases. Moreover, studies have found that Res can reduce xanthine oxidase (XO), serum uric acid level, uric acid excretion fraction and blood urea nitrogen to normal state,. In the mouse with hyperuricemia, the expression of ATP-binding cassette subfamily G member 2 in ileum was activated by acetylation PGC-1α/PPARγ pathway after SIRT1 activation by Res, reducing the level of serum uric acid, thus exerting an anti-hyperuricemia effect. Additionally, hyperuricemia promotes the proliferation of vascular smooth muscle cells (VSMCs) via activating the renin-angiotensin-aldosterone system, causing renal vasoconstriction and glomerular arterial wall thickening,. Ma et al. found that Simiao pill restores high fructose-induced hyperuricemia and metabolic syndrome by up-regulating SIRT1 in glomerular of mice with high-fructose, inhibiting NF-κB pathway and the activation of NOD-like receptor pyrin domain containing 3 (NLRP3) inflammasome, improving interstitial infiltration of nephritis cells and glomerular injury and reducing urinary albumin level. Polydatin has also been shown to inhibit NF-κB/NLRP3 through the AMPK/SIRT1 pathway, thereby reducing potassium oxonate-induced hyperuricemia and renal inflammation. Xu et al. also found that hyperuricemia was associated with decreased SIRT1, phosphorylation of downstream target molecules FOXO3a, increased expression of androgen receptor, XO and deacetylation of NF-κB subunit p65. Importantly, they further found that hyperuricemia is more frequent and widespread in men with nonalcoholic fatty liver disease (NAFLD) than in women, which is intimately contributed to the inhibition of SIRT1 signaling pathway induced by hyperuricemia,. Interestingly, elevated estrogen levels caused by SIRT1 may also be responsible for treatment of hyperuricemia. H Sumino pointed out that postmenopausal women with hyperuricemia are treated with hormone replacement therapy to reduce serum uric acid level,. In conclusion, these studies suggest that SIRT1 may be a potential target of hyperuricemia and its complications, which is of great significance for further clinical research and application.
Hypertension
Hypertension is a major risk factor for premature death and disability worldwide,. The pathogenesis of hypertension can also lead to dysfunction of the nervous system, endocrine system and immune system. The information connection between these systems is mainly accomplished by neuropeptides and endocrine hormones, including neuropeptide Y, angiotensin II (Ang II), arginine-vasopressin, endothelin and NO. Ryohei et al. reported that Res suppresses the expression of AT1R in the mouse aorta by activating SIRT1 and ameliorates Ang II-induced hypertension. Meanwhile, overexpression of SIRT1 reduces the expression of AT1R, while SIRT1 inhibitor (nicotinamide) reverses this effect. Further studies showed that the suppression of AT1R depends on the most proximal promoter region, which contains the Sp1 binding site (GC box). GC box mutation of luciferase construct failed to respond to Res, suggesting that Sp1 site plays an important role in Res-induced AT1R downregulation. Nicotinamide phosphoribosyl transferase (NAMPT) is a potential cardiovascular protective effect of adipose cytokines, which plays an important role in DNA damage repair and prevent premature VSMCs in aging, and is also a key enzyme regulating NAD+ biosynthesis and SIRT1 activity,. The overexpression of NAMPT partially inhibits Ang II-induced elevated ROS levels by regulating SIRT1 and the concentration of NAD+, thus relieving Ang II-induced hypertension. This observation suggests that NAMPT may regulate the occurrence of hypertension through SIRT1. In addition, endothelial dysfunction is also considered as a possible early key link in the occurrence of hypertension. Extracellular vesicles collected from induced pluripotent stem cell-derived mesenchymal stem cells, may reduce age-related endothelial dysfunction, arteriosclerosis, and hypertension by activating the SIRT1-AMPKα-eNOS pathway. Grape seed proanthocyanidin extracts (GSPE) indirectly up-regulates SIRT1 and inhibits aortic NO production disorder, improving hypertension and showing the potential of anti-inflammatory, antioxidant, anti-ageing and regulation of endothelial function -. Klotho, an ageing-suppressor gene, whose mutations results in significant increases in pulse wave velocity and blood pressure. Importantly, Gao et al., pointed out that serum Klotho deficiency in hypertensive patients is associated with significantly reduced activity of AMPKα, SIRT1, and eNOS in aortic endothelial cells (ECs), along with collagen expression and elastin breakdown. Conversely, activation of SIRT1 functionally interacts with AMPKα, up-regulates phosphorylation of AMPKα and then activates eNOS, inhibits ROS accumulation and oxidative stress in aortic ECs and leads to vascular remodeling, down-regulates collagen expression and elastin breakage, predicting the improvement of aortic sclerosis and hypertension.
Polycystic ovarian syndrome
PCOS is the most common endocrine and metabolic disordered disease in the women,. This may be the result of hypothalamo-pituitary ovarian axis disorder, follicular membrane cells or granulosa cells (GC) dysfunction, and metabolic abnormalities -. PCOS is associated with specific reproductive health complications, including lower oocyte quality and clinical pregnancy rates in assisted conception cycles. Metformin, an anti-aging agent, is approved for the treatment of PCOS. Clinical trials and observational studies have found that metformin can prevent or mitigate PCOS through SIRT1-related pathways. Increased testosterone level is the pathological feature of PCOS patients, and when the PCOS patients are treated with Res, the level of serum testosterone decreases, the number of secondary and closed follicles increases, while Graafian follicles decrease. It was further found that the combination of metformin and Res induce the antioxidant and anti-inflammatory systems of PCOS by activating SIRT1 and AMPK, thereby improving the weight gain, hormone levels and follicular cell structure of PCOS. Tao et al. found that SIRT1 expression in PCOS group is significantly lower than that in the control group in the establishment of PCOS rat induced by dehydroepiandrosterone, and shows the loss of estrous cycle, saccular dilatation of the follicle, reduce luteal number, and thickens follicular membrane cell layer. The researcher also found that both metformin and exenatide improve reproductive endocrine function in PCOS rats via the AMPKα-SIRT1 pathway. It is suggested that the deficiency of SIRT1 and estrogen promotes the occurrence of diseases related to female reproductive development. In addition, quercetin can up-regulate the expressions of AMPK and SIRT1 in ovarian tissues, and reverse the changes of adiponectin, visfatin and resistin in adipose tissues of PCOS rats, thus maintaining hormone and metabolic balance. Interestingly, SIRT1 knockdown in human ovarian GC inhibits estrogen synthesis activity and aromatase. Previous studies have pointed out that SIRT1 regulates non-histone activity and affects aromatase transcription regulation. However, enhanced aromatase activity will increase PCOS susceptibility. SIRT1 plays an important role in the genesis and development of PCOS, which provides a basis for the development of potential therapeutic methods to improve the metabolism and reproductive function of PCOS.
Osteoporosis
Osteoporosis is the disease induced by genetic and environmental interference with the endocrine system. With aging, the decrease of NAD+ leads to the decrease in bone progenitor cells and bone mass, accompanied by the imbalance in the number and activity of osteoblasts and osteoclasts,. Menopausal, ovariectomized female mice and aged male mice exhibit decreased SIRT1, osteoporosis and bone injury. Meanwhile, SIRT1 knockout mice, as well as osteoblast and osteoclast specific knockout, show a low bone mass phenotype. Significantly reduced bone mass, reduced bone formation and increased bone marrow adipose formation are observed in female SIRT1 haplo-insufficient (Sirt1+/-) mice, along with osteoarthritis,. Importantly, clinical studies have identified the potential of SIRT1 in predicting and treating related diseases such as osteoporosis and osteonecrosis. SIRT1 expression in femoral neck was significantly reduced in patients with osteoporosis. Additionally, in 16 female patients with osteoporosis, there is a negative correlation between SIRT1 activity in peripheral blood mononuclear cells and C-terminal cross-linking telopeptide of type I collagen, the marker of bone resorption in serum.
Besides, overexpression of SIRT1 inhibits H2O2-induced osteoblast apoptosis by activating the FOXO1/β-catenin pathway. One estrogen, 17β-E2 (10-6 M) up-regulates SIRT1, p-AMPK and FOXO3a in osteoblasts, thereby inhibiting osteoblast apoptosis by promoting autophagy, while the protective effect of autophagy may be attributed to reducing intracellular oxidative damage and maintaining cell structure and function. Res and endoplasmic reticulum stress (ERS) inhibitor 4-PBA significantly inhibit osteoclast differentiation and osteolysis. Activation of SIRT1 can regulate the activity of osteoclasts and osteoblasts and improve bone metabolism, thereby reducing osteoporosis. In conclusion, SIRT1 plays a positive role in maintaining bone homeostasis, bone mineralization and bone resorption, which also brings hope for the treatment of osteoporosis.
Diabetes
As a metabolic disease, diabetes is characterized by defective insulin secretion or insulin dysfunction leading to impaired islet beta cell function. Study confirmed that the SIRT1 level was always lower in patients with poor glycaemic control than in those with good glycaemic control. In the isolated rat islets, SIRT1-mediated NF-κB deacetylation inhibits iNOS and cytokine-mediated beta cell damage. SIRT1 activation also promotes beta cell recovery and endocrine progenitor differentiation. These studies revealed that SIRT1 plays an active role in regulating insulin secretion. Notably, direct sequencing and exon sequencing of a patient with type 1 diabetes revealed t-to-C exchange in SIRT1 exon 1 and excessive production of nitric oxide, cytokines and chemokines, suggesting that SIRT1 mutation may be a potential weakness of patients with diabetes. There are many strategies and drugs for the treatment of diabetes in clinic, among which metformin is the star of clinical drug. Hyperglycemia induced expression of inflammatory genes, NF-κB and the proapoptotic gene Bax in bovine retinal capillary endothelial cells (BRECs) and diabetic rat's retinas. BRECs with knockdown SIRT1 increases sensitivity to hyperglycemic stress, while SIRT1 overexpression or metformin activation inhibit mitochondrial ROS-mediated PARP activity and glyceraldehyde-3-phosphate dehydrogenase through upregulation of LKB1/AMPK, and ultimately inhibiting NF-κB and Bax expression. It was proved that metformin may be associated with the SIRT1/LKB1/AMPK pathway in inhibiting diabetic retinopathy. High glucose treatment significantly reduces the expression of SIRT1 protein in mouse microvascular ECs. However, overexpression of SIRT1 or metformin can attenuate the decreased expression of SIRT1 induced by high glucose, thus regulating downstream targets FOXO1 and p53/p21, and protecting ECs from high glucose-induced premature aging. In addition, SIRT1 is also involved in the occurrence of other diabetes-related diseases. Decreased hepatic glucose production in type 2 diabetes rats with reduced hepatic SIRT1 levels, and systemic SIRT1 activation induced by drugs or genes can prevent dietary diabetes. Knockout of SIRT1 leads to hyperglycemia and insulin resistance in the liver. Importantly, the positive effect of SIRT1 has also been confirmed in diabetic nephropathy, and diabetic cardiomyopathy.
Hyperlipidemia
Hyperlipidemia is a common disease of dyslipidemia caused by endocrine and metabolic disorders,. Hyperlipidemia is clinically divided into the following categories: hypercholesterolemia, hypertriglyceridemia, mixed hyperlipidemia and atherosclerotic dyslipidemia. SIRT1 is the major regulatory factor of lipid and carbohydrate metabolism. The reduction of SIRT1 will cause metabolic disorders, fatty liver and obesity. Reciprocally, enhancing the activity of SIRT1 may normalize abnormal fat morphology and abnormal expression of lipid metabolism markers, thus regulating cholesterol and lipid metabolism,. SIRT1 is involved in the caspase-1 pathway in early hyperlipidemia and promotes ECs activation prior to monocyte recruitment. In addition, SIRT1 is closely associated with lipid metabolism markers, including PPARα/γ, SREBP, Liver X Receptor α (LXRα) and low-density lipoprotein (LDL) receptor. For example, the accumulation of oxidized LDL (oxLDL) in peritoneal macrophages of SIRT1-deficient mice increases and promotes the formation of foam cells. SIRT1 reduces the expression of lectin-like oxLDL receptor-1 by inhibiting NF-κB signaling pathway, thus reducing oxLDL uptake and alleviating atherosclerosis. SIRT1 also leads to lipolysis of mature adipocytes by enhancing the activity of PPARα and directly deacetylates SREBP during fasting, which leads to inhibition of lipid synthesis and fat storage. In addition, PPARα may indirectly affect lipid synthesis through cross-talk with SREBP and exploit the advantages to the full in regulating cellular fatty acid and cholesterol homeostasis,. AMPK is a nutrition-sensing molecule which correspondingly reduces fatty acid synthesis. Increased SIRT1 and AMPK activity inhibits dysregulation of lipids and obese phenotypes. In the hyperlipidemia-induced hepatic steatosis and atherosclerotic mice, SIRT1 restores cholesterol efflux caused by hyperlipidemia through regulating the LXRα/β-PPARγ pathway. Notably, there are several compounds which alleviates lipid metabolism diseases such as hyperlipidemia by activating SIRT1. As the cofactor of SIRT1, nicotinic acid increases p-AMPK and SIRT1 in adipocytes and myotube, reduces total cholesterol, cholesterol esters, plasma triglycerides, and lessens the size of atherosclerotic lesions and lipid area. Ginsenoside Rb2 prevents hepatic lipid accumulation in vivo and in vitro through SIRT1-mediated autophagy induction. Melatonin improves serum biochemical markers and liver morphological damage, and inhibits oxidative stress through its antioxidant properties and upregulation of SIRT1. Importantly, He et al. assessed the association between serum SIRT1 levels and coronary atherosclerotic plaque characteristics by computed tomography angiography (CTA) and Framingham Risk Score generation in each patient. The results showed that serum SIRT1 level is significantly reduced in the non-high-risk plaque group. It is suggested that SIRT1 may play a predictive role in coronary artery pre-CTA plaque screening. These evidences confirm the positive effect of SIRT1 activation on hyperlipidemia.
In conclusion, SIRT1 has a significant protective effect on a variety of endocrine diseases, such as hyperuricemia, hypertension, polycystic ovarian syndrome, osteoporosis, by regulating a variety of target genes (Figure 3). Importantly, SIRT1 have been widely studied in clinical practice and gradually become key molecules in the treatment of endocrine and metabolic diseases and aging related diseases.
Application of SIRT1 agonists in endocrine and metabolic diseases
A large number of studies have shown that SIRT1 has positive effects on a variety of diseases, along with the development of different SIRT1 activators, including Res, SRT2183, SRT1460, SRT1720, SRT2104 and SRT3025 (Table 1).
Res
Res is a natural polyphenol with strong biological activity, also known as astragalus triphenol. Res has been paid attention to by the medical community, with anti-oxidation, antibacterial, anti-inflammatory, anti-aging and estrogen-like activities -. Many formulations containing Res have been shown to be beneficial in healthy, obese male by reducing lipid content, circulating glucose, triglycerides and inflammatory markers in the liver -. The combination of Res with SIRT1 promotes the conformational change of SIRT1 and enhances its activity. Res affects thyroid function by enhancing iodide ion capture, and increases thyrotropin secretion by activating SIRT1. It also enhances insulin sensitivity and reduces hepatic glucose production. In addition, Res promotes browning in a SIRT1-dependent manner and has a beneficial effect on excess fat utilization, suggesting potential therapeutic application of Res in the treatment of obesity and related metabolic disorders. Sara et al. systematically analyzed the effects of Res in animal and clinical studies. Many animal studies have reported beneficial effects of Res on sex hormones, gonadotropins, and blood glucose. In particular, Res improves ovarian volume, high-quality oocyte rate, high-quality embryo rate, androgen, and gonadotropin concentration in PCOS patients. A meta-analysis was conducted to review the effects of Res intake on weight loss. This study showed that the supplementation of Res significantly reduces body weight, body mass index, waist circumference, and fat mass, and increases lean mass. It is worth noting that a clinical study assessed the effects of short-term high-dose Res administration on intestinal and hepatic lipoprotein turnover and insulin sensitivity in non-diabetic, overweight, and obese male who had mild hypertriglyceridemia. Res was given at doses of 1000 mg/day for one week and increased to 2000 mg/day the second week. In this study, Res improved glucose tolerance without causing any adverse reactions, however, there was no significant effect on insulin sensitivity and plasma triglyceride content, which may be related to the time and concentration of the drug. Notably, Res has a positive effect on metabolism (URL: www.clinicaltrials.gov. Unique Identifier: NCT01451918.). Interestingly, Res reduced cerebrospinal fluid (CSF) metalloproteinase 9 (MMP9), modulated neuroinflammation, improved mild-to-moderate Alzheimer's disease, and induced adaptive immunity. SIRT1 activation may be a viable target for the treatment or prevention of neurodegenerative diseases. Additionally, in vivo res pretreatment confers neuroprotection similar to ischemic preconditioning (IPC) via the SIRT1-UCP2 (mitochondrial uncoupling protein 2) pathway. Furthermore, potential effect modifications by sex, smoking and vascular risk factors of the SIRT/UCP genes in the associations with atherosclerotic plaque. Meanwhile, polymorphisms in SIRT6/UCP1 genes may be important for increased carotid plaque burden and echodensity, but translation of these findings to an individual risk of cerebrovascular events needs further investigation. These basic studies and randomized controlled trials provide potential evidence for the clinical application and development of Res as a daily dietary supplement.
SRT3025
As the SIRT1 small molecule activator with oral activity, SRT3025 increases the expression of hepatic LDL receptors and accumulation of proprotein convertase subtilisin/kexin type 9 (Pcsk9), reduces plasma cholesterol level, inhibits inflammatory response and atherosclerosis. Estrogen deficiency can lead to rapid bone loss and skeletal fragility. Oral administration of SRT3025 (50 and 100 mg/kg/d) for 6 weeks completely reverses the harmful effects of ovariectomy on bone mass and bone structure. SRT3025 achieves its therapeutic effect by decreasing the expression of bone sclerostin, increasing cortical periosteal mineralizing surface and serum propeptide of type I procollagen (a bone formation marker). Additionally, SIRT1 inhibitor EX-527 reverses the positive effects of SRT3025 in vitro. This study provides a theoretical basis for SRT3025 in metabolic and age-related diseases such as osteoporosis. Diabetic mice treated with SRT3025 has significantly improved blood glucose, reduced islet alpha cell mass and decreased plasma glucagon concentration. Consistent with the decrease in glucagon abundance, overexpression of key gluconeogenic enzymes, glucose-6-phosphatase and phosphoenolpyruvate carboxykinase (PCK1), which are associated with diabetes, are also decreased by SRT3025. In addition, pharmacological activation of SIRT1 by SRT3025 increases the expression of several thermogenic genes FOXC2, PGC-1α, Dio2, TFAM and Cyc1 in C3HT101/2 cells. Notably, SRT3025 treatment increases PGC-1α mRNA and protein levels through activating SIRT1 in femoral MSCs in female patients undergoing hip operations caused by fracture or osteoarthritis. These evidences confirm that SRT3025 activates SIRT1 and upregulates PGC-1α to stimulate a thermogenic gene program in mouse and human bone marrow adipocytes. SRT3025 inhibits the expression of sclerotin in osteocytes and thus inhibits age-related bone loss. Importantly, a phase I clinical trial of SRT3025 at different doses in the treatment of diabetes has been completed (NCT01340911). This evidence will provide outstanding guidance for the development and application of SIRT1 agonists.
SRT2183
SRT2183, a selective SIRT1 activator, can bind to SIRT1 enzym-peptide substrate complex, reduces the Michaelis constant for acetylated substrates, and directly activates SIRT1 through allosteric mechanism,. The EC1.5 (the compound concentration required to increase enzyme activity by 50%) of SRT2183 is about 0.36 μM, and the maximum activation is 296%. SRT2183 reduces the acetylation of SIRT1 substrate p53. SRT2183 is used as a positive control in SIRT1 deacetylation because of its good tolerability. SRT2183 activates the expression of AMPK and SIRT1 and reduces the acetylation level of lysine 310 of RelA/p65. In bone marrow macrophages, SRT2183 inhibits RANKL-induced osteoclast formation and resorption ability, suggesting that SRT2183 plays a positive role in bone metabolism. Moreover, high glucose exposure induced the expression of p53, SIRT1 and AMPK in HepG2 cells. SRT2183 reverses this result and reduces triglyceride accumulation and cytoplasmic oxidative stress. In addition, many metabolic syndromes are associated with reduced kidney function, and the medulla is critical in regulating water and sodium balance and maintaining normal blood pressure. Activated SIRT1 by SRT2183 reduces apoptosis and increases fibrosis in unilateral ureteral obstruction. Recent studies have shown that SRT2183 also inhibits the growth of ovarian cancer cells. In terms of mechanism, SRT2183 has anti-ovarian cancer effects by activating the apoptosis pathway and increasing the level of LC3II, enhancing the degradation of p62/SQSTM1, and inducing the maturation of autophagosomes. However, compared with other SIRT1 agonists, there are few studies on SRT2183 at the present stage, especially in animal experiments. Further studies are needed to explore SIRT1-related agonist differences and feedback regulation in endocrine and metabolic pathways.
CAY10602
VASANTHA et al. performed a high-throughput screening of 147,000 compounds. Compounds with relative percentages greater than or equal to 150 are considered definitive SIRT1 activators. CAY10602 increases SIRT1 activation and significantly inhibits TNF-α expression. As a cytokine generated by macrophages, TNF-α is involved in adipose tissue metabolism and endocrine function,. High-fat-diet increases body weight, serum total cholesterol, triglycerides, aspartate aminotransferase, alanine aminotransferase, blood glucose, insulin levels, and liver malondialdehyde, while decreases liver superoxide dismutase activity. These changes are negatively correlated with SIRT1 and PGC-1α. HepG2 hepatocytes cell line exposed to oleic acid (OA) for 48 h shows decreased cell viability, apoptosis, lipid accumulation and ROS production, while pretreatment with CAY10602 at 20μM for 2h reverses this effect. On the contrary, pretreatment with Tenovin-6 aggravates the effect of OA on hepG2. CAY10602 restores phosphorylation of eNOS (p-eNOS), p-AMPK, and phosphorylation of Akt (p-Akt) levels inhibited by high glucose in diabetic mice. These results suggest that CAY10602 contributes to the beneficial effects of SIRT1 on endothelial function in diabetes and obesity.
Others
In addition to Res, SRT3025, CAY10602, and SRT2183, there are many other small molecular compounds that can activate SIRT1, including SRT1460, SRT1720, and SRT2104. The EC1.5 of SRT1460 is 2.9μM and the maximum activation rate is 447%. The dissociation constant and reaction enthalpy of SRT1460 confirm that SRT1460 binds to a SIRT1-peptide substrate complex and promotes a more productive conformation that improves catalytic activity. In addition, SRT1720 is also a small molecule activator of SIRT1 with an EC1.5 of 0.16 μM and a maximum activation value of 781%. SRT1720 has a clear protective effect on diabetic nephropathy, which originates from that SRT1720 inhibits the expression of HIF1α, GLUT1 and SNAIL, thereby reducing glomerular hypertrophy, mesangial expansion, glomerulosclerosis, and interstitial fibrosis. SRT1720 also up-regulates the expressions of SIRT1, SIRT6, FOXO3a and NRF-1, inhibits the expressions of mTORC1, p-MTOR, p-P70S6K, NF-κB and p53, improves the follicular reserve of diet-induced obese female mice, and prolongs the ovarian life. SRT2104 inhibits dysfunction in ECs treated with high glucose. It is worth noting that natural products also have a positive effect on regulating endocrine and metabolic diseases. For example, naringenin and hesperetin help to improve impaired thyroid function in the old-aged rats. Isoflavonoid can affect the expression of SIRT1 and regulate the electrophysiology of hypothalamic neurons related to the secretion of gonadotropin-releasing hormone (GnRH), controlling hormone release and reproductive maturation. In addition, vitamin D, melatonin, natural carotene, berberine, ferulic acid and other natural products affect the expression of SIRT1 to varying degrees, and then participate in the regulation of endocrine and metabolic systems.
Application of SIRT1 inhibitors EX527 in endocrine and metabolic diseases
In addition, inhibitors of SIRT1 have also been widely studied, including EX527 (Selisistat), Sirtinol, Inauhzin, SIRT1/2 Inhibitor IV. EX527 has been widely studied and applied in a variety of diseases. For example, In DM mice, EX527 inhibited promyelocytic zinc finger protein (PLZF) and insulin induced by Far-infrared (FIR) radiation, respectively. SIRT1 upregulation also increased Ca+V1.2 expression and calcium influx, promoting insulin secretion in β-cells. In addition, studies have shown that fucoglycan (FO) isolated from brown algae can ameliorate pancreatic β-cell injury and impaired insulin synthesis under diabetic conditions, and improve hyperglycemia, lower expression of SIRT1, PDX-1, and GLP-1R in the pancreas of diabetic mice. EX527 plays an important auxiliary role in this study, which can significantly reverse the beneficial effects of FO. Similarly, EX527 blocks the protective effect of curcumin on MIN6 (a mouse insulinoma cell line) cells exposed to HO. The above evidence suggests a significant protective effect of SIRT1 in diabetes mellitus.
Conclusion and Perspectives
SIRT1, a protein deacetylase dependent on NAD+, has long been considered as an evolutionarily conserved life-regulating factor and is associated with many aging-related diseases. With the further study of SIRT1, another potential role of SIRT1 has been discovered -- the energy sensor of the body. SIRT1 is involved in hormone regulation, energy uptake, circadian rhythm, and metabolism. It also has potential therapeutic applications in cardiovascular disease, cancer and age-related diseases. The loss of SIRT1 leads to abnormal secretion of some hormones and metabolic disorders. SIRT1 regulates the function of pancreatic beta cells, improves insulin sensitivity and increases insulin secretion,. It has also been reported that Res, flavonoids and other compounds also affects insulin secretion by regulating the activity of SIRT1 in glucose-dependent insulin secretion,. These evidences suggest that SIRT1 is a key target of glucose metabolism and insulin resistance. In an orthotopic transplantation rat cholangiocarcinoma (CCA) model, the SIRT1 inhibitor sirtinol reduced tumor size and tumorigenic proteins (glioma-associated oncogene 1, phosphorylated extracellular signal-regulated kinase, and IL-6) expression. In addition, SIRT1 has been shown to promote progression of colorectal cancer. SIRT1 also plays a key role in gout/hyperuricemia, hypertension, hyperlipidaemia and other diseases. For example, SIRT1 regulate metabolist-related target molecules, including PPARγ, SREBP and LXRα, to improve the lipid metabolic environment. It has been reported that SIRT1 is closely related to adiponectin, leptin or resistance derived from adipose tissue, and the level of adiponectin is positively correlated with SIRT1, which can be used as an endocrine signal to mediate the browning of white adipose tissues. Myeloid-specific SIRT1 knockout increases hepatic steatosis and hypothalamic inflammation in mice fed a high-fat diet. In addition, SIRT1 is also involved in regulating the secretion of thyroid hormones, testosterone, aldosterone, estrogen, glucagon cortisol and pituitary hormone. At the same time, a variety of small molecules compounds and natural products can act on SIRT1 to different degrees, and our current research has also confirmed that SIRT1 plays an important role in the development of endocrine and metabolic disorders. Notably, the above effects may be caused by different action mechanisms of SIRT1 streets, such as SIRT1/Keap1/Nrf2/HO-1 and PI3K/Akt/GSK-3β mediated oxidative stress, SIRT1/NF-κB mediated inflammatory response, SIRT1/PGC1α mediated mitochondrial damage, and SIRT1/FOXO mediated autophagy. These evidences provide a theoretical basis for SIRT1 as a therapeutic target for endocrine and metabolic diseases.
However, endocrine and metabolic regulation is a complex process, and the above two aspects interact with each other. Moreover, the treatment targeting SIRT1 is still in the preliminary stage. More basic research and more clinical trials are needed before patients can benefit from SIRT1-targeted therapies. Further research may focus on, 1) comprehensively expounding the complex regulatory mechanism of SIRT1 in endocrine and metabolic systems. 2) Exploring the degree of SIRT1's involvement in regulating energy homeostasis and its sensitivity to energy under physiological conditions. 3) Developing standards for assessing SIRT1 expression, especially SIRT1 content in blood and hormone, sugar and lipid metabolism levels, so as to predict endocrine and metabolic diseases. 4) Endocrine and metabolic diseases are closely related to daily diet. How can the body maintain appropriate SIRT1 levels to protect the body from lipid and glucose metabolism disorders? 5) Studying whether SIRT1 targeted therapy has suboptimal efficacy in clinical application. In conclusion, this review provides a comprehensive overview of SIRT1's role in endocrine and metabolic diseases and provides theoretical basis for SIRT1's potential as a novel therapeutic target.
References 239
- 1.
Targeting sirtuin 1 to improve metabolism: all you need is NAD(+)? Pharmacological reviews. 2012;64:166-87.
Not in our library10.1124/pr.110.003905
- 2.
- 3.
Calorie restriction-the SIR2 connection. Cell. 2005;120:473-82.
Not in our library10.1016/j.cell.2005.01.029
- 4.
Sirtuin 1 and sirtuin 3: physiological modulators of metabolism. Physiological reviews. 2012;92:1479-514.
Not in our library10.1152/physrev.00022.2011
- 5.
Targeting Sirt-1 controls GVHD by inhibiting T-cell allo-response and promoting Treg stability in mice. Blood. 2019;133:266-79.
Not in our library10.1182/blood-2018-07-863233
- 6.
Age-Associated Sirtuin 1 Reduction in Vascular Smooth Muscle Links Vascular Senescence and Inflammation to Abdominal Aortic Aneurysm. Circulation research. 2016;119:1076-88.
Not in our library10.1161/circresaha.116.308895
- 7.
Melatonin improved rat cardiac mitochondria and survival rate in septic heart injury. Journal of pineal research. 2013;55:1-6.
Not in our library10.1111/jpi.12033
- 8.
- 9.
SIRT1/FOXO3a axis plays an important role in the prevention of mandibular bone loss induced by 1,25(OH)(2)D deficiency. International journal of biological sciences. 2020;16:2712-26.
Not in our library10.7150/ijbs.48169
- 10.
SIRT1 interacts with metabolic transcriptional factors in the pancreas of insulin-resistant and calorie-restricted rats. Molecular biology reports. 2013;40:3373-80.
Not in our library10.1007/s11033-012-2412-3
- 11.
Perfluorooctane sulfonate continual exposure impairs glucose-stimulated insulin secretion via SIRT1-induced upregulation of UCP2 expression. Environmental pollution (Barking, Essex: 1987). 2021;278:116840.
Not in our library10.1016/j.envpol.2021.116840
- 12.
Role of sirtuin 1 in the regulation of hepatic gene expression by thyroid hormone. The Journal of biological chemistry. 2013;288:807-18.
Not in our library10.1074/jbc.m112.437970
- 13.
Estrogen-SIRT1 Axis Plays a Pivotal Role in Protecting Arteries Against Menopause-Induced Senescence and Atherosclerosis. Journal of atherosclerosis and thrombosis. 2020;27:47-59.
Not in our library10.5551/jat.47993
- 14.
Sirt1 regulates testosterone biosynthesis in Leydig cells via modulating autophagy. Protein & cell. 2021;12:67-75.
Not in our library10.1007/s13238-020-00771-1
- 15.
Sirt1 inhibits the transcription factor CREB to regulate pituitary growth hormone synthesis. FASEB journal: official publication of the Federation of American Societies for Experimental Biology. 2013;27:1561-71.
Not in our library10.1096/fj.12-220129
- 16.
Increased Sirt1 secreted from visceral white adipose tissue is associated with improved glucose tolerance in obese Nrf2-deficient mice. Redox biology. 2021;38:101805.
Not in our library10.1016/j.redox.2020.101805
- 17.
Resveratrol activates duodenal Sirt1 to reverse insulin resistance in rats through a neuronal network. Nature medicine. 2015;21:498-505.
Not in our library10.1038/nm.3821
- 18.
Polydatin attenuates potassium oxonate-induced hyperuricemia and kidney inflammation by inhibiting NF-κB/NLRP3 inflammasome activation via the AMPK/SIRT1 pathway. Food & function. 2017;8:1785-92.
Not in our library10.1039/c6fo01561a
- 19.
Glutaredoxin-1 Deficiency Causes Fatty Liver and Dyslipidemia by Inhibiting Sirtuin-1. Antioxidants & redox signaling. 2017;27:313-27.
Not in our library10.1089/ars.2016.6716
- 20.
The angiogenic factor PlGF mediates a neuroimmune interaction in the spleen to allow the onset of hypertension. Immunity. 2014;41:737-52.
Not in our library10.1016/j.immuni.2014.11.002
- 21.
The SIR2/3/4 complex and SIR2 alone promote longevity in Saccharomyces cerevisiae by two different mechanisms. Genes & development. 1999;13:2570-80.
Not in our library10.1101/gad.13.19.2570
- 22.
Cloning and characterization of four SIR genes of Saccharomyces cerevisiae. Molecular and cellular biology. 1986;6:688-702.
Not in our library10.1128/mcb.6.2.688-702.1986
- 23.
Increased dosage of a sir-2 gene extends lifespan in Caenorhabditis elegans. Nature. 2001;410:227-30.
Not in our library10.1038/35065638
- 24.
Sir2 mediates longevity in the fly through a pathway related to calorie restriction. Proceedings of the National Academy of Sciences of the United States of America. 2004;101:15998-6003.
Not in our library10.1073/pnas.0404184101
- 25.
- 26.
The role of sirtuins in the control of metabolic homeostasis. Annals of the New York Academy of Sciences. 2009;1173(Suppl 1):E10-9.
Not in our library10.1111/j.1749-6632.2009.04952.x
- 27.
Sirtuin functions in health and disease. Molecular endocrinology (Baltimore, Md). 2007;21:1745-55.
Not in our library10.1210/me.2007-0079
- 28.
Chromosomal characterization and localization of the NAD+-dependent histone deacetylase gene sirtuin 1 in the mouse. International journal of molecular medicine. 2009;23:245-52.
Not in our library
- 29.
The biochemistry of sirtuins. Annual review of biochemistry. 2006;75:435-65.
Not in our library10.1146/annurev.biochem.74.082803.133500
- 30.
NAD⁺/NADH metabolism and NAD⁺-dependent enzymes in cell death and ischemic brain injury: current advances and therapeutic implications. Current medicinal chemistry. 2015;22:1239-47.
Not in our library10.2174/0929867322666150209154420
- 31.
Human SirT1 interacts with histone H1 and promotes formation of facultative heterochromatin. Molecular cell. 2004;16:93-105.
Not in our library10.1016/j.molcel.2004.08.031
- 32.
- 33.
Resveratrol up-regulates SIRT1 and inhibits cellular oxidative stress in the diabetic milieu: mechanistic insights. The Journal of nutritional biochemistry. 2012;23:699-705.
Not in our library10.1016/j.jnutbio.2011.03.012
- 34.
Downregulation of SIRT1 signaling underlies hepatic autophagy impairment in glycogen storage disease type Ia. PLoS genetics. 2017;13:e1006819.
Not in our library10.1371/journal.pgen.1006819
- 35.
TSPYL2 is a novel regulator of SIRT1 and p300 activity in response to DNA damage. Cell death and differentiation. 2019;26:918-31.
Not in our library10.1038/s41418-018-0168-6
- 36.
AMPK promotes p53 acetylation via phosphorylation and inactivation of SIRT1 in liver cancer cells. Cancer research. 2012;72:4394-404.
Not in our library10.1158/0008-5472.can-12-0429
- 37.
Ubiquitination-mediated degradation of SIRT1 by SMURF2 suppresses CRC cell proliferation and tumorigenesis. Oncogene. 2020;39:4450-64.
Not in our library10.1038/s41388-020-1298-0
- 38.
- 39.
Novel role of silent information regulator 1 in myocardial ischemia. Circulation. 2013;128:2232-40.
Not in our library10.1161/circulationaha.113.002480
- 40.
The Role of Sirtuin-1 in Immune Response and Systemic Lupus Erythematosus. Frontiers in immunology. 2021;12:632383.
Not in our library10.3389/fimmu.2021.632383
- 41.
SIRT1 and insulin resistance. Nature reviews Endocrinology. 2009;5:367-73.
Not in our library10.1038/nrendo.2009.101
- 42.
How does SIRT1 affect metabolism, senescence and cancer? Nature reviews Cancer. 2009;9:123-8.
Not in our library10.1038/nrc2562
- 43.
- 44.
Interplay Between Diabetes and Pancreatic Ductal Adenocarcinoma and Insulinoma: The Role of Aging, Genetic Factors, and Obesity. Frontiers in endocrinology. 2020;11:563267.
Not in our library10.3389/fendo.2020.563267
- 45.
SIRT1 Activation Promotes β-Cell Regeneration by Activating Endocrine Progenitor Cells via AMPK Signaling-Mediated Fatty Acid Oxidation. Stem cells (Dayton, Ohio). 2019;37:1416-28.
Not in our library10.1002/stem.3073
- 46.
GABA protects pancreatic beta cells against apoptosis by increasing SIRT1 expression and activity. Biochemical and biophysical research communications. 2014;452:649-54.
Not in our library10.1016/j.bbrc.2014.08.135
- 47.
Activation of SIRT1 protects pancreatic β-cells against palmitate-induced dysfunction. Biochimica et biophysica acta. 2012;1822:1815-25.
Not in our library10.1016/j.bbadis.2012.08.009
- 48.
SIRT1 deacetylates FOXA2 and is critical for Pdx1 transcription and β-cell formation. International journal of biological sciences. 2013;9:934-46.
Not in our library10.7150/ijbs.7529
- 49.
Pancreas-Specific Sirt1-Deficiency in Mice Compromises Beta-Cell Function without Development of Hyperglycemia. PloS one. 2015;10:e0128012.
Not in our library10.1371/journal.pone.0128012
- 50.
Endocrine autoimmune diseases and female infertility. Nature reviews Endocrinology. 2014;10:37-50.
Not in our library10.1038/nrendo.2013.212
- 51.
Extra- and intra-ovarian factors in polycystic ovary syndrome: impact on oocyte maturation and embryo developmental competence. Human reproduction update. 2011;17:17-33.
Not in our library10.1093/humupd/dmq032
- 52.
Interactions between androgens, FSH, anti-Müllerian hormone and estradiol during folliculogenesis in the human normal and polycystic ovary. Human reproduction update. 2016;22:709-24.
Not in our library10.1093/humupd/dmw027
- 53.
Melatonin attenuates postovulatory oocyte dysfunction by regulating SIRT1 expression. Reproduction (Cambridge, England). 2018;156:81-92.
Not in our library10.1530/rep-18-0211
- 54.
Resveratrol promotes white adipocytes browning and improves metabolic disorders in Sirt1-dependent manner in mice. FASEB journal: official publication of the Federation of American Societies for Experimental Biology. 2020;34:4527-39.
Not in our library10.1096/fj.201902222r
- 55.
- 56.
SIRT1 is downregulated by autophagy in senescence and ageing. Nature cell biology. 2020;22:1170-9.
Not in our library10.1038/s41556-020-00579-5
- 57.
SIRT1 facilitates primordial follicle recruitment independent of deacetylase activity through directly modulating Akt1 and mTOR transcription. FASEB journal: official publication of the Federation of American Societies for Experimental Biology. 2019;33:14703-16.
Not in our library10.1096/fj.201900782r
- 58.
Sirt1 sustains female fertility by slowing age-related decline in oocyte quality required for post-fertilization embryo development. Aging cell. 2020;19:e13204.
Not in our library10.1111/acel.13204
- 59.
NMNAT2-mediated NAD(+) generation is essential for quality control of aged oocytes. Aging cell. 2019;18:e12955.
Not in our library10.1111/acel.12955
- 60.
Exploring the role of autophagy during early human embryonic development through single-cell transcriptome and methylome analyses. Science China Life sciences. 2022;65:940-52.
Not in our library10.1007/s11427-021-1948-1
- 61.
Melatonin protects against chronic stress-induced oxidative meiotic defects in mice MII oocytes by regulating SIRT1. Cell cycle (Georgetown, Tex). 2020;19:1677-95.
Not in our library10.1080/15384101.2020.1767403
- 62.
Putrescine delays postovulatory aging of mouse oocytes by upregulating PDK4 expression and improving mitochondrial activity. Aging. 2018;10:4093-106.
Not in our library10.18632/aging.101699
- 63.
Therapeutic and Mechanistic Approaches of Tridax Procumbens Flavonoids for the Treatment of Osteoporosis. Current drug targets. 2020;21:1687-702.
Not in our library10.2174/1389450121666200719012116
- 64.
Beneficial effect of resveratrol on phenotypic features and activity of osteoarthritic osteoblasts. Arthritis research & therapy. 2017;19:151.
Not in our library10.1186/s13075-017-1365-2
- 65.
Synthesis and Application of Iron Oxide Nanoparticles in Bone Tissue Repair %J Journal of Nanomaterials. 2021. 2021.
Not in our library
- 66.
- 67.
The role of osteocalcin in the endocrine cross-talk between bone remodelling and energy metabolism. Diabetologia. 2011;54:1291-7.
Not in our library10.1007/s00125-011-2155-z
- 68.
Sirt1 overexpression protects murine osteoblasts against TNF-α-induced injury in vitro by suppressing the NF-κB signaling pathway. Acta pharmacologica Sinica. 2012;33:668-74.
Not in our library10.1038/aps.2011.189
- 69.
Transcription factor Runx2 and its application to bone tissue engineering. Stem cell reviews and reports. 2012;8:891-7.
Not in our library10.1007/s12015-011-9337-4
- 70.
Post-translational Regulation of Runx2 in Bone and Cartilage. Journal of dental research. 2009;88:693-703.
Not in our library10.1177/0022034509341629
- 71.
Atorvastatin promotes bone formation in aged apoE(-/-) mice through the Sirt1-Runx2 axis. Journal of orthopaedic surgery and research. 2020;15:303.
Not in our library10.1186/s13018-020-01841-0
- 72.
Resveratrol promotes osteogenesis of human mesenchymal stem cells by upregulating RUNX2 gene expression via the SIRT1/FOXO3A axis. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2011;26:2552-63.
Not in our library10.1002/jbmr.460
- 73.
The role of SIRT1 in BMP2-induced chondrogenic differentiation and cartilage maintenance under oxidative stress. Aging. 2020;12:9000-13.
Not in our library10.18632/aging.103161
- 74.
The polyphenol resveratrol promotes skeletal growth in mice through a sirtuin 1-bone morphogenic protein 2 longevity axis. British journal of pharmacology. 2018;175:4183-92.
Not in our library10.1111/bph.14477
- 75.
Microfluidic systems for studying dynamic function of adipocytes and adipose tissue. Analytical and bioanalytical chemistry. 2018;410:791-800.
Not in our library10.1007/s00216-017-0741-8
- 76.
Sirt1 attenuates camptothecin-induced apoptosis through caspase-3 pathway in porcine preadipocytes. Experimental cell research. 2013;319:670-83.
Not in our library10.1016/j.yexcr.2012.12.025
- 77.
Adipocyte SIRT1 controls systemic insulin sensitivity by modulating macrophages in adipose tissue. EMBO reports. 2017;18:645-57.
Not in our library10.15252/embr.201643184
- 78.
Doses of Quercetin in the Range of Serum Concentrations Exert Delipidating Effects in 3T3-L1 Preadipocytes by Acting on Different Stages of Adipogenesis, but Not in Mature Adipocytes. Oxidative medicine and cellular longevity. 2015;2015:480943.
Not in our library10.1155/2015/480943
- 79.
Sirt1 promotes fat mobilization in white adipocytes by repressing PPAR-gamma. Nature. 2004;429:771-6.
Not in our library10.1038/nature02583
- 80.
Brown remodeling of white adipose tissue by SirT1-dependent deacetylation of Pparγ. Cell. 2012;150:620-32.
Not in our library10.1016/j.cell.2012.06.027
- 81.
Adipose Tissue and FoxO1: Bridging Physiology and Mechanisms. Cells. 2020.
Not in our library10.3390/cells9040849
- 82.
Role of FoxO1 in FFA-induced oxidative stress in adipocytes. American journal of physiology Endocrinology and metabolism. 2007;293:E159-64.
Not in our library10.1152/ajpendo.00629.2006
- 83.
SIRT1 controls lipolysis in adipocytes via FOXO1-mediated expression of ATGL. Journal of lipid research. 2011;52:1693-701.
Not in our library10.1194/jlr.m014647
- 84.
Fucosterol, isolated from Ecklonia stolonifera, inhibits adipogenesis through modulation of FoxO1 pathway in 3T3-L1 adipocytes. The Journal of pharmacy and pharmacology. 2017;69:325-33.
Not in our library10.1111/jphp.12684
- 85.
Shear stress, SIRT1, and vascular homeostasis. Proceedings of the National Academy of Sciences of the United States of America. 2010;107:10268-73.
Not in our library10.1073/pnas.1003833107
- 86.
Mechanisms underlying caloric restriction and lifespan regulation: implications for vascular aging. Circulation research. 2008;102:519-28.
Not in our library10.1161/circresaha.107.168369
- 87.
The case for uric acid-lowering treatment in patients with hyperuricaemia and CKD. Nature reviews Nephrology. 2019;15:767-75.
Not in our library10.1038/s41581-019-0174-z
- 88.
Relationship between serum uric acid and cerebral white matter lesions in the elderly. Nutrition, metabolism, and cardiovascular diseases: NMCD. 2012;22:154-9.
Not in our library10.1016/j.numecd.2010.06.005
- 89.
Study on the correlation between constituents detected in serum from Rhizoma Smilacis Glabrae and the reduction of uric acid levels in hyperuricemia. Journal of ethnopharmacology. 2013;150:747-54.
Not in our library10.1016/j.jep.2013.09.024
- 90.
Anti-hyperuricemic and nephroprotective effects of Smilax china L. Journal of ethnopharmacology. 2011;135:399-405.
Not in our library10.1016/j.jep.2011.03.033
- 91.
SIRT1 prevents hyperuricemia via the PGC-1α/PPARγ-ABCG2 pathway. Endocrine. 2016;53:443-52.
Not in our library10.1007/s12020-016-0896-7
- 92.
Association between uric acid, renal haemodynamics and arterial stiffness over the natural history of type 1 diabetes. Diabetes, obesity & metabolism. 2019;21:1388-98.
Not in our library10.1111/dom.13665
- 93.
Uric acid and angiotensin II additively promote inflammation and oxidative stress in human proximal tubule cells by activation of toll-like receptor 4. Journal of cellular physiology. 2019;234:10868-76.
Not in our library10.1002/jcp.27929
- 94.
Simiao pill ameliorates renal glomerular injury via increasing Sirt1 expression and suppressing NF-κB/NLRP3 inflammasome activation in high fructose-fed rats. Journal of ethnopharmacology. 2015;172:108-17.
Not in our library10.1016/j.jep.2015.06.015
- 95.
Treating hyperuricemia related non-alcoholic fatty liver disease in rats with resveratrol. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2019;110:844-9.
Not in our library10.1016/j.biopha.2018.12.039
- 96.
Gender effect of hyperuricemia on the development of nonalcoholic fatty liver disease (NAFLD): A clinical analysis and mechanistic study. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2019;117:109158.
Not in our library10.1016/j.biopha.2019.109158
- 97.
Reduction of serum uric acid by hormone replacement therapy in postmenopausal women with hyperuricaemia. Lancet (London, England). 1999;354:650.
Not in our library10.1016/s0140-6736(99)92381-4
- 98.
17-β Oestradiol prevents cardiovascular dysfunction in post-menopausal metabolic syndrome by affecting SIRT1/AMPK/H3 acetylation. British journal of pharmacology. 2013;170:779-95.
Not in our library10.1111/bph.12290
- 99.
The global epidemiology of hypertension. Nature reviews Nephrology. 2020;16:223-37.
Not in our library10.1038/s41581-019-0244-2
- 100.
Hypertension-induced cognitive impairment: from pathophysiology to public health. Nature reviews Nephrology. 2021;17:639-54.
Not in our library10.1038/s41581-021-00430-6
- 101.
Device Therapy of Hypertension. Circulation research. 2021;128:1080-99.
Not in our library10.1161/circresaha.121.318091
- 102.
Genetic screening in arterial hypertension. Nature reviews Endocrinology. 2017;13:289-98.
Not in our library10.1038/nrendo.2016.196
- 103.
Hypertension: Do Inflammation and Immunity Hold the Key to Solving this Epidemic? Circulation research. 2021;128:908-33.
Not in our library10.1161/circresaha.121.318052
- 104.
Neuroimmune crosstalk in the pathophysiology of hypertension. Nature reviews Cardiology. 2019;16:476-90.
Not in our library10.1038/s41569-019-0178-1
- 105.
Microglial Cells Impact Gut Microbiota and Gut Pathology in Angiotensin II-Induced Hypertension. Circulation research. 2019;124:727-36.
Not in our library10.1161/circresaha.118.313882
- 106.
GABAergic excitation of vasopressin neurons: possible mechanism underlying sodium-dependent hypertension. Circulation research. 2013;113:1296-307.
Not in our library10.1161/circresaha.113.301814
- 107.
Current role of neprilysin inhibitors in hypertension and heart failure. Pharmacology & therapeutics. 2014;144:41-9.
Not in our library10.1016/j.pharmthera.2014.05.002
- 108.
Oxidative Stress, GTPCH1, and Endothelial Nitric Oxide Synthase Uncoupling in Hypertension. Antioxidants & redox signaling. 2021;34:750-64.
Not in our library10.1089/ars.2020.8112
- 109.
SIRT1, a longevity gene, downregulates angiotensin II type 1 receptor expression in vascular smooth muscle cells. Arteriosclerosis, thrombosis, and vascular biology. 2008;28:1263-9.
Not in our library10.1161/atvbaha.108.166991
- 110.
SIRT1-Mediated eNAMPT Secretion from Adipose Tissue Regulates Hypothalamic NAD+ and Function in Mice. Cell metabolism. 2015;21:706-17.
Not in our library10.1016/j.cmet.2015.04.002
- 111.
Nicotinamide Phosphoribosyltransferase in Smooth Muscle Cells Maintains Genome Integrity, Resists Aortic Medial Degeneration, and Is Suppressed in Human Thoracic Aortic Aneurysm Disease. Circulation research. 2017;120:1889-902.
Not in our library10.1161/circresaha.116.310022
- 112.
NAMPT/SIRT1 Attenuate Ang II-Induced Vascular Remodeling and Vulnerability to Hypertension by Inhibiting the ROS/MAPK Pathway. Oxidative medicine and cellular longevity. 2020;2020:1974265.
Not in our library10.1155/2020/1974265
- 113.
Argininosuccinate Lyase Deficiency Causes an Endothelial-Dependent Form of Hypertension. American journal of human genetics. 2018;103:276-87.
Not in our library10.1016/j.ajhg.2018.07.008
- 114.
Stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension. Journal of extracellular vesicles. 2020;9:1783869.
Not in our library10.1080/20013078.2020.1783869
- 115.
Protective effects of a novel niacin-bound chromium complex and a grape seed proanthocyanidin extract on advancing age and various aspects of syndrome X. Annals of the New York Academy of Sciences. 2002;957:250-9.
Not in our library10.1111/j.1749-6632.2002.tb02921.x
- 116.
Selective inhibition by grape seed proanthocyanidin extracts of cell adhesion molecule expression induced by advanced glycation end products in endothelial cells. Journal of cardiovascular pharmacology. 2006;48:47-53.
Not in our library10.1097/01.fjc.0000242058.72471.0c
- 117.
Grape seed proanthocyanidin extracts enhance endothelial nitric oxide synthase expression through 5'-AMP activated protein kinase/Surtuin 1-Krüpple like factor 2 pathway and modulate blood pressure in ouabain induced hypertensive rats. Biological & pharmaceutical bulletin. 2012;35:2192-7.
Not in our library10.1248/bpb.b12-00598
- 118.
Activation of SIRT1 Attenuates Klotho Deficiency-Induced Arterial Stiffness and Hypertension by Enhancing AMP-Activated Protein Kinase Activity. Hypertension (Dallas, Tex: 1979). 2016;68:1191-9.
Not in our library10.1161/hypertensionaha.116.07709
- 119.
Autophagy in ovary and polycystic ovary syndrome: role, dispute and future perspective. Autophagy. 2021;17:2706-33.
Not in our library10.1080/15548627.2021.1938914
- 120.
Adipocyte and steroidogenic cell cross-talk in polycystic ovary syndrome. Human reproduction update. 2021;27:771-96.
Not in our library10.1093/humupd/dmab004
- 121.
Polycystic ovary syndrome: definition, aetiology, diagnosis and treatment. Nature reviews Endocrinology. 2018;14:270-84.
Not in our library10.1038/nrendo.2018.24
- 122.
Follicle dynamics and anovulation in polycystic ovary syndrome. Human reproduction update. 2008;14:367-78.
Not in our library10.1093/humupd/dmn015
- 123.
Energy sensors and reproductive hypothalamo-pituitary ovarian axis (HPO) in female mammals: Role of mTOR (mammalian target of rapamycin), AMPK (AMP-activated protein kinase) and SIRT1 (Sirtuin 1). Molecular and cellular endocrinology. 2021;521:111113.
Not in our library10.1016/j.mce.2020.111113
- 124.
Metformin for the treatment of the polycystic ovary syndrome. The New England journal of medicine. 2008;358:47-54.
Not in our library10.1056/nejmct0707092
- 125.
Metformin for Cardiovascular Protection, Inflammatory Bowel Disease, Osteoporosis, Periodontitis, Polycystic Ovarian Syndrome, Neurodegeneration, Cancer, Inflammation and Senescence: What Is Next? ACS pharmacology & translational science. 2021;4:1747-70.
Not in our library10.1021/acsptsci.1c00167
- 126.
- 127.
Expression of SIRT1 in the ovaries of rats with polycystic ovary syndrome before and after therapeutic intervention with exenatide. International journal of clinical and experimental pathology. 2015;8:8276-83.
Not in our library
- 128.
Effects of metformin and Exenatide on insulin resistance and AMPKα-SIRT1 molecular pathway in PCOS rats. Journal of ovarian research. 2019;12:86.
Not in our library10.1186/s13048-019-0555-8
- 129.
Therapeutic potential of quercetin in an animal model of PCOS: Possible involvement of AMPK/SIRT-1 axis. European journal of pharmacology. 2021;900:174062.
Not in our library10.1016/j.ejphar.2021.174062
- 130.
Effects of BMAL1-SIRT1-positive cycle on estrogen synthesis in human ovarian granulosa cells: an implicative role of BMAL1 in PCOS. Endocrine. 2016;53:574-84.
Not in our library10.1007/s12020-016-0961-2
- 131.
Follicle-stimulating hormone/cAMP regulation of aromatase gene expression requires beta-catenin. Proceedings of the National Academy of Sciences of the United States of America. 2006;103:12435-40.
Not in our library10.1073/pnas.0603006103
- 132.
Insulin, osteoblasts, and energy metabolism: why bone counts calories. The Journal of clinical investigation. 2014;124:1465-7.
Not in our library10.1172/jci75554
- 133.
Osteoporosis: now and the future. Lancet (London, England). 2011;377:1276-87.
Not in our library10.1016/s0140-6736(10)62349-5
- 134.
A decrease in NAD(+) contributes to the loss of osteoprogenitors and bone mass with aging. NPJ aging and mechanisms of disease. 2021;7:8.
Not in our library10.1038/s41514-021-00058-7
- 135.
Role of sirtuins in bone biology: Potential implications for novel therapeutic strategies for osteoporosis. Aging cell. 2021;20:e13301.
Not in our library10.1111/acel.13301
- 136.
- 137.
Sirt1 is a regulator of bone mass and a repressor of Sost encoding for sclerostin, a bone formation inhibitor. Endocrinology. 2011;152:4514-24.
Not in our library10.1210/en.2011-1128
- 138.
Increased apoptotic chondrocytes in articular cartilage from adult heterozygous SirT1 mice. Annals of the rheumatic diseases. 2012;71:613-6.
Not in our library10.1136/ard.2011.200504
- 139.
Reduced Sirtuin1 expression at the femoral neck in women who sustained an osteoporotic hip fracture. Osteoporosis international: a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 2016;27:2373-8.
Not in our library10.1007/s00198-016-3536-4
- 140.
Sirtuin 1 activity in peripheral blood mononuclear cells of patients with osteoporosis. Medical science monitor basic research. 2014;20:142-5.
Not in our library10.12659/msmbr.891372
- 141.
Upregulation of SIRT1 inhibits H2O2-induced osteoblast apoptosis via FoxO1/β-catenin pathway. Molecular medicine reports. 2018;17:6681-90.
Not in our library10.3892/mmr.2018.8657
- 142.
Up-regulation of SIRT1 induced by 17beta-estradiol promotes autophagy and inhibits apoptosis in osteoblasts. Aging. 2021;13:23652-71.
Not in our library10.18632/aging.203639
- 143.
NADPH Oxidase Isoforms Are Involved in Glucocorticoid-Induced Preosteoblast Apoptosis. Oxidative medicine and cellular longevity. 2019;2019:9192413.
Not in our library10.1155/2019/9192413
- 144.
Particle-induced SIRT1 downregulation promotes osteoclastogenesis and osteolysis through ER stress regulation. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2018;104:300-6.
Not in our library10.1016/j.biopha.2018.05.030
- 145.
Resveratrol-mediated SIRT-1 interactions with p300 modulate receptor activator of NF-kappaB ligand (RANKL) activation of NF-kappaB signaling and inhibit osteoclastogenesis in bone-derived cells. The Journal of biological chemistry. 2011;286:11492-505.
Not in our library10.1074/jbc.m110.198713
- 146.
Class IA phosphatidylinositol 3-kinase in pancreatic β cells controls insulin secretion by multiple mechanisms. Cell metabolism. 2010;12:619-32.
Not in our library10.1016/j.cmet.2010.11.005
- 147.
Poor glycaemic control in type 2 diabetes patients reduces endothelial progenitor cell number by influencing SIRT1 signalling via platelet-activating factor receptor activation. Diabetologia. 2013;56:162-72.
Not in our library10.1007/s00125-012-2749-0
- 148.
Sirtuin 1 in lipid metabolism and obesity. Annals of medicine. 2011;43:198-211.
Not in our library10.3109/07853890.2010.547211
- 149.
Identification of a SIRT1 mutation in a family with type 1 diabetes. Cell metabolism. 2013;17:448-55.
Not in our library10.1016/j.cmet.2013.02.001
- 150.
Sirtuin 1-mediated cellular metabolic memory of high glucose via the LKB1/AMPK/ROS pathway and therapeutic effects of metformin. Diabetes. 2012;61:217-28.
Not in our library10.2337/db11-0416
- 151.
Metformin modulates hyperglycaemia-induced endothelial senescence and apoptosis through SIRT1. British journal of pharmacology. 2014;171:523-35.
Not in our library10.1111/bph.12496
- 152.
SirT1 knockdown in liver decreases basal hepatic glucose production and increases hepatic insulin responsiveness in diabetic rats. Proceedings of the National Academy of Sciences of the United States of America. 2009;106:11288-93.
Not in our library10.1073/pnas.0812931106
- 153.
Hepatic Sirt1 deficiency in mice impairs mTorc2/Akt signaling and results in hyperglycemia, oxidative damage, and insulin resistance. The Journal of clinical investigation. 2011;121:4477-90.
Not in our library10.1172/jci46243
- 154.
Role of transcription factor acetylation in diabetic kidney disease. Diabetes. 2014;63:2440-53.
Not in our library10.2337/db13-1810
- 155.
Resveratrol improves oxidative stress and protects against diabetic nephropathy through normalization of Mn-SOD dysfunction in AMPK/SIRT1-independent pathway. Diabetes. 2011;60:634-43.
Not in our library10.2337/db10-0386
- 156.
Melatonin prevents Drp1-mediated mitochondrial fission in diabetic hearts through SIRT1-PGC1α pathway. Journal of pineal research. 2018;65:e12491.
Not in our library10.1111/jpi.12491
- 157.
Endocrine functions of bile acids. The EMBO journal. 2006;25:1419-25.
Not in our library10.1038/sj.emboj.7601049
- 158.
Susceptibility gene discovery for common metabolic and endocrine traits. Journal of molecular endocrinology. 2002;28:1-17.
Not in our library10.1677/jme.0.0280001
- 159.
Underutilization of aspirin for primary prevention of cardiovascular disease among HIV-infected patients. Clinical infectious diseases: an official publication of the Infectious Diseases Society of America. 2012;55:1550-7.
Not in our library10.1093/cid/cis752
- 160.
Development of a dietary-induced metabolic syndrome model using miniature pigs involvement of AMPK and SIRT1. European journal of clinical investigation. 2015;45:70-80.
Not in our library10.1111/eci.12370
- 161.
SIRT1 activator E1231 protects from experimental atherosclerosis and lowers plasma cholesterol and triglycerides by enhancing ABCA1 expression. Atherosclerosis. 2018;274:172-81.
Not in our library10.1016/j.atherosclerosis.2018.04.039
- 162.
Parental SIRT1 Overexpression Attenuate Metabolic Disorders Due to Maternal High-Fat Feeding. International journal of molecular sciences. 2020.
Not in our library10.3390/ijms21197342
- 163.
Early hyperlipidemia promotes endothelial activation via a caspase-1-sirtuin 1 pathway. Arteriosclerosis, thrombosis, and vascular biology. 2015;35:804-16.
Not in our library10.1161/atvbaha.115.305282
- 164.
Conserved role of SIRT1 orthologs in fasting-dependent inhibition of the lipid/cholesterol regulator SREBP. Genes & development. 2010;24:1403-17.
Not in our library10.1101/gad.1901210
- 165.
Fasting and fasting-mimicking treatment activate SIRT1/LXRα and alleviate diabetes-induced systemic and microvascular dysfunction. Diabetologia. 2021;64:1674-89.
Not in our library10.1007/s00125-021-05431-5
- 166.
Cinnamon as Dietary Supplement Caused Hyperlipidemia in Healthy Rats. Evidence-based complementary and alternative medicine: eCAM. 2021;2021:9892088.
Not in our library10.1155/2021/9892088
- 167.
SIRT1 decreases Lox-1-mediated foam cell formation in atherogenesis. European heart journal. 2010;31:2301-9.
Not in our library10.1093/eurheartj/ehq107
- 168.
Profiling of promoter occupancy by PPARalpha in human hepatoma cells via ChIP-chip analysis. Nucleic acids research. 2010;38:2839-50.
Not in our library10.1093/nar/gkq012
- 169.
PPARα-dependent Insig2a overexpression inhibits SREBP-1c processing during fasting. Scientific reports. 2017;7:9958.
Not in our library10.1038/s41598-017-10523-7
- 170.
SIRT1 regulates hepatocyte lipid metabolism through activating AMP-activated protein kinase. The Journal of biological chemistry. 2008;283:20015-26.
Not in our library10.1074/jbc.m802187200
- 171.
Metformin opposes impaired AMPK and SIRT1 function and deleterious changes in core clock protein expression in white adipose tissue of genetically-obese db/db mice. Diabetes, obesity & metabolism. 2011;13:1097-104.
Not in our library10.1111/j.1463-1326.2011.01466.x
- 172.
Hyperlipidemia Determines Dysfunctional HDL Production and Impedes Cholesterol Efflux in the Small Intestine: Alleviation by Ginger Extract. Molecular nutrition & food research. 2019;63:e1900029.
Not in our library10.1002/mnfr.201900029
- 173.
Erratum: Leucine-nicotinic acid synergy stimulates AMPK/Sirt1 signaling and regulates lipid metabolism and lifespan in Caenorhabditis elegans, and hyperlipidemia and atherosclerosis in mice. American journal of cardiovascular disease. 2017;7:97.
Not in our library
- 174.
Ginsenoside Rb2 Alleviates Hepatic Lipid Accumulation by Restoring Autophagy via Induction of Sirt1 and Activation of AMPK. International journal of molecular sciences. 2017.
Not in our library10.3390/ijms18051063
- 175.
Melatonin Modulation of Sirtuin-1 Attenuates Liver Injury in a Hypercholesterolemic Mouse Model. BioMed research international. 2018;2018:7968452.
Not in our library10.1155/2018/7968452
- 176.
Low serum level of sirtuin 1 predicts coronary atherosclerosis plaques during computed tomography angiography among an asymptomatic cohort. Coronary artery disease. 2019;30:621-5.
Not in our library10.1097/mca.0000000000000804
- 177.
- 178.
Resveratrol improves adipose insulin signaling and reduces the inflammatory response in adipose tissue of rhesus monkeys on high-fat, high-sugar diet. Cell metabolism. 2013;18:533-45.
Not in our library10.1016/j.cmet.2013.09.004
- 179.
Sirt1 activation protects the mouse renal medulla from oxidative injury. The Journal of clinical investigation. 2010;120:1056-68.
Not in our library10.1172/jci41563
- 180.
SIRT1-Activating Compounds (STAC) Negatively Regulate Pancreatic Cancer Cell Growth and Viability Through a SIRT1 Lysosomal-Dependent Pathway. Clinical cancer research: an official journal of the American Association for Cancer Research. 2016;22:2496-507.
Not in our library10.1158/1078-0432.ccr-15-1760
- 181.
Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes. Nature. 2007;450:712-6.
Not in our library10.1038/nature06261
- 182.
The Selective Sirtuin 1 Activator SRT2104 Reduces Endotoxin-Induced Cytokine Release and Coagulation Activation in Humans. Critical care medicine. 2015;43:e199-202.
Not in our library10.1097/ccm.0000000000000949
- 183.
The Sirt1 activator SRT3025 provides atheroprotection in Apoe-/- mice by reducing hepatic Pcsk9 secretion and enhancing Ldlr expression. European heart journal. 2015;36:51-9.
Not in our library10.1093/eurheartj/ehu095
- 184.
Effects of resveratrol on collagen type II protein in the superficial and middle zone chondrocytes of porcine articular cartilage. Journal of ethnopharmacology. 2016;178:25-33.
Not in our library10.1016/j.jep.2015.11.047
- 185.
Molecular mechanisms of action of resveratrol in modulation of diabetic and non-diabetic cardiomyopathy. Pharmacological research. 2020;161:105112.
Not in our library10.1016/j.phrs.2020.105112
- 186.
Resveratrol (RV): A pharmacological review and call for further research. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2021;143:112164.
Not in our library10.1016/j.biopha.2021.112164
- 187.
- 188.
Is the use of resveratrol in the treatment and prevention of obesity premature? Nutrition research reviews. 2009;22:111-7.
Not in our library10.1017/s0954422409990084
- 189.
Calorie restriction-like effects of 30 days of resveratrol supplementation on energy metabolism and metabolic profile in obese humans. Cell metabolism. 2011;14:612-22.
Not in our library10.1016/j.cmet.2011.10.002
- 190.
High-dose resveratrol treatment for 2 weeks inhibits intestinal and hepatic lipoprotein production in overweight/obese men. Arteriosclerosis, thrombosis, and vascular biology. 2013;33:2895-901.
Not in our library10.1161/atvbaha.113.302342
- 191.
Mechanism of human SIRT1 activation by resveratrol. The Journal of biological chemistry. 2005;280:17187-95.
Not in our library10.1074/jbc.m501250200
- 192.
Resveratrol increases iodide trapping in the rat thyroid cell line FRTL-5. Thyroid: official journal of the American Thyroid Association. 2010;20:195-203.
Not in our library10.1089/thy.2009.0171
- 193.
Resveratrol and Markers of Polycystic Ovary Syndrome: a Systematic Review of Animal and Clinical Studies. Reproductive sciences (Thousand Oaks, Calif). 2021.
Not in our library10.1007/s43032-021-00653-9
- 194.
The effects of resveratrol intake on weight loss: a systematic review and meta-analysis of randomized controlled trials. Critical reviews in food science and nutrition. 2020;60:375-90.
Not in our library10.1080/10408398.2018.1529654
- 195.
Resveratrol pretreatment protects rat brain from cerebral ischemic damage via a sirtuin 1-uncoupling protein 2 pathway. Neuroscience. 2009;159:993-1002.
Not in our library10.1016/j.neuroscience.2009.01.017
- 196.
Sirtuin/uncoupling protein gene variants and carotid plaque area and morphology. International journal of stroke: official journal of the International Stroke Society. 2015;10:1247-52.
Not in our library10.1111/ijs.12623
- 197.
The Sirtuin1 activator SRT3025 down-regulates sclerostin and rescues ovariectomy-induced bone loss and biomechanical deterioration in female mice. Endocrinology. 2014;155:3508-15.
Not in our library10.1210/en.2014-1334
- 198.
SIRT1 activation attenuates α cell hyperplasia, hyperglucagonaemia and hyperglycaemia in STZ-diabetic mice. Scientific reports. 2018;8:13972.
Not in our library10.1038/s41598-018-32351-z
- 199.
Sirt1 Promotes a Thermogenic Gene Program in Bone Marrow Adipocytes: From Mice to (Wo)Men. Frontiers in endocrinology. 2019;10:126.
Not in our library10.3389/fendo.2019.00126
- 200.
Advanced oxidation protein products aggravate age-related bone loss by increasing sclerostin expression in osteocytes via ROS-dependent downregulation of Sirt1. International journal of molecular medicine. 2021.
Not in our library10.3892/ijmm.2021.4941
- 201.
Targeting sirtuin-1 in Huntington's disease: rationale and current status. CNS drugs. 2013;27:345-52.
Not in our library10.1007/s40263-013-0055-0
- 202.
- 203.
A novel inverse relationship between metformin-triggered AMPK-SIRT1 signaling and p53 protein abundance in high glucose-exposed HepG2 cells. American journal of physiology Cell physiology. 2012;303:C4-c13.
Not in our library10.1152/ajpcell.00296.2011
- 204.
Sirtuins and renal diseases: relationship with aging and diabetic nephropathy. Clinical science (London, England: 1979). 2013;124:153-64.
Not in our library10.1042/cs20120190
- 205.
SRT2183 impairs ovarian cancer by facilitating autophagy. Aging. 2020;12:24208-18.
Not in our library10.18632/aging.104126
- 206.
SIRT1 modulating compounds from high-throughput screening as anti-inflammatory and insulin-sensitizing agents. Journal of biomolecular screening. 2006;11:959-67.
Not in our library10.1177/1087057106294710
- 207.
Macrophages and dendritic cells infiltrating islets with or without beta cells produce tumour necrosis factor-alpha in patients with recent-onset type 1 diabetes. Diabetologia. 2007;50:596-601.
Not in our library10.1007/s00125-006-0569-9
- 208.
Adipose tissue dysfunction in obesity, diabetes, and vascular diseases. European heart journal. 2008;29:2959-71.
Not in our library10.1093/eurheartj/ehn387
- 209.
Elucidation of SIRT-1/PGC-1α-associated mitochondrial dysfunction and autophagy in nonalcoholic fatty liver disease. Lipids in health and disease. 2021;20:40.
Not in our library10.1186/s12944-021-01461-5
- 210.
Resveratrol ameliorates endothelial dysfunction in diabetic and obese mice through sirtuin 1 and peroxisome proliferator-activated receptor δ. Pharmacological research. 2019;139:384-94.
Not in our library10.1016/j.phrs.2018.11.041
- 211.
SRT1720 retards renal fibrosis via inhibition of HIF1α /GLUT1 in diabetic nephropathy. The Journal of endocrinology. 2019.
Not in our library10.1530/joe-18-0536
- 212.
SIRT1 activator (SRT1720) improves the follicle reserve and prolongs the ovarian lifespan of diet-induced obesity in female mice via activating SIRT1 and suppressing mTOR signaling. Journal of ovarian research. 2014;7:97.
Not in our library10.1186/s13048-014-0097-z
- 213.
SRT2104 attenuates diabetes-induced aortic endothelial dysfunction via inhibition of P53. The Journal of endocrinology. 2018;237:1-14.
Not in our library10.1530/joe-17-0672
- 214.
Citrus Flavanones Upregulate Thyrotroph Sirt1 and Differently Affect Thyroid Nrf2 Expressions in Old-Aged Wistar Rats. Journal of agricultural and food chemistry. 2020;68:8242-54.
Not in our library10.1021/acs.jafc.0c03079
- 215.
Genistein affects gonadotrophin-releasing hormone secretion in GT1-7 cells via modulating kisspeptin receptor and key regulators. Systems biology in reproductive medicine. 2022;68:138-50.
Not in our library10.1080/19396368.2021.2003910
- 216.
Randomized study of the effects of vitamin D and/or magnesium supplementation on mood, serum levels of BDNF, inflammation, and SIRT1 in obese women with mild to moderate depressive symptoms. Nutritional neuroscience. 2021;1-13.
Not in our library10.1080/1028415x.2021.1945859
- 217.
- 218.
The Natural Carotenoid Crocetin and the Synthetic Tellurium Compound AS101 Protect the Ovary against Cyclophosphamide by Modulating SIRT1 and Mitochondrial Markers. Oxidative medicine and cellular longevity. 2017;2017:8928604.
Not in our library10.1155/2017/8928604
- 219.
Berberine Alleviates Oxidative Stress in Islets of Diabetic Mice by Inhibiting miR-106b Expression and Up-Regulating SIRT1. Journal of cellular biochemistry. 2017;118:4349-57.
Not in our library10.1002/jcb.26089
- 220.
Ferulic acid protects against radiation-induced testicular damage in male rats: impact on SIRT1 and PARP1. Environmental science and pollution research international. 2018;25:6218-27.
Not in our library10.1007/s11356-017-0873-6
- 221.
SIRT inhibitors induce cell death and p53 acetylation through targeting both SIRT1 and SIRT2. Molecular cancer therapeutics. 2010;9:844-55.
Not in our library10.1158/1535-7163.mct-09-0971
- 222.
Sirtuin activators and inhibitors. BioFactors (Oxford, England). 2012;38:349-59.
Not in our library10.1002/biof.1032
- 223.
A small molecule Inauhzin inhibits SIRT1 activity and suppresses tumour growth through activation of p53. EMBO molecular medicine. 2012;4:298-312.
Not in our library10.1002/emmm.201100211
- 224.
Current advances in the synthesis and antitumoral activity of SIRT1-2 inhibitors by modulation of p53 and pro-apoptotic proteins. Current medicinal chemistry. 2012;19:5871-84.
Not in our library10.2174/092986712804143303
- 225.
Far-infrared radiation prevents decline in β-cell mass and function in diabetic mice via the mitochondria-mediated Sirtuin1 pathway. Metabolism: clinical and experimental. 2020;104:154143.
Not in our library10.1016/j.metabol.2020.154143
- 226.
Fucoidan ameliorates pancreatic β-cell death and impaired insulin synthesis in streptozotocin-treated β cells and mice via a Sirt-1-dependent manner. Molecular nutrition & food research. 2017.
Not in our library10.1002/mnfr.201700136
- 227.
Curcumin ameliorates HO-induced injury through SIRT1-PERK-CHOP pathway in pancreatic beta cells. Acta biochimica et biophysica Sinica. 2022;54:370-7.
Not in our library10.3724/abbs.2022004
- 228.
SIRT1 regulates macrophage self-renewal. The EMBO journal. 2017;36:2353-72.
Not in our library10.15252/embj.201695737
- 229.
Prepregnancy consumption of fruits and fruit juices and the risk of gestational diabetes mellitus: a prospective cohort study. Diabetes care. 2012;35:1079-82.
Not in our library10.2337/dc11-2105
- 230.
Histone Deacetylase Sirtuin 1 Promotes Loss of Primary Cilia in Cholangiocarcinoma. Hepatology (Baltimore, Md). 2021;74:3235-48.
Not in our library10.1002/hep.32080
- 231.
SIRT1-Mediated Expression of CD24 and Epigenetic Suppression of Novel Tumor Suppressor miR-1185-1 Increases Colorectal Cancer Stemness. Cancer research. 2020;80:5257-69.
Not in our library10.1158/0008-5472.can-19-3188
- 232.
Adiponectin/SIRT1 Axis Induces White Adipose Browning After Vertical Sleeve Gastrectomy of Obese Rats with Type 2 Diabetes. Obesity surgery. 2020;30:1392-403.
Not in our library10.1007/s11695-019-04295-4
- 233.
Myeloid-specific deletion of SIRT1 increases hepatic steatosis and hypothalamic inflammation in mice fed a high-fat diet. Metabolic brain disease. 2014;29:635-43.
Not in our library10.1007/s11011-014-9542-3
- 234.
Sirtuins and their relevance to the kidney. Journal of the American Society of Nephrology: JASN. 2010;21:1620-7.
Not in our library10.1681/asn.2010010046
- 235.
The Nutrient and Energy Sensor Sirt1 Regulates the Hypothalamic-Pituitary-Adrenal (HPA) Axis by Altering the Production of the Prohormone Convertase 2 (PC2) Essential in the Maturation of Corticotropin-releasing Hormone (CRH) from Its Prohormone in Male Rats. The Journal of biological chemistry. 2016;291:5844-59.
Not in our library10.1074/jbc.m115.675264
- 236.
Sirtuin1 Maintains Actin Cytoskeleton by Deacetylation of Cortactin in Injured Podocytes. Journal of the American Society of Nephrology: JASN. 2015;26:1939-59.
Not in our library10.1681/asn.2014030289
- 237.
- 238.
SIRT1 activation ameliorates hyperglycaemia by inducing a torpor-like state in an obese mouse model of type 2 diabetes. Diabetologia. 2015;58:819-27.
Not in our library10.1007/s00125-014-3485-4
- 239.
Leucine-nicotinic acid synergy stimulates AMPK/Sirt1 signaling and regulates lipid metabolism and lifespan in Caenorhabditis elegans, and hyperlipidemia and atherosclerosis in mice. American journal of cardiovascular disease. 2017;7:33-47.
Not in our library
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