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Updated mechanisms of MASLD pathogenesis

Yuxuan Li, Peipei Yang, Jialu Ye and 3 more

Lipids in Health and Disease · 2024 · Review · CC BY

doi:10.1186/s12944-024-02108-x

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) has garnered considerable attention globally. Changing lifestyles, over-nutrition, and physical inactivity have promoted its development. MASLD is typically accompanied by obesity and is strongly linked to metabolic syndromes. Given that MASLD prevalence is on the rise, there is an urgent need to elucidate its pathogenesis. Hepatic lipid accumulation generally triggers lipotoxicity and induces MASLD or progress to metabolic dysfunction-associated steatohepatitis (MASH) by mediating endoplasmic reticulum stress, oxidative stress, organelle dysfunction, and ferroptosis. Recently, significant attention has been directed towards exploring the role of gut microbial dysbiosis in the development of MASLD, offering a novel therapeutic target for MASLD. Considering that there are no recognized pharmacological therapies due to the diversity of mechanisms involved in MASLD and the difficulty associated with undertaking clinical trials, potential targets in MASLD remain elusive. Thus, this article aimed to summarize and evaluate the prominent roles of lipotoxicity, ferroptosis, and gut microbes in the development of MASLD and the mechanisms underlying their effects. Furthermore, existing advances and challenges in the treatment of MASLD were outlined.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 21, 2026. Paragraph numbers are ours, so an answer can point at one.

Introduction

Nonalcoholic fatty liver disease (NAFLD) is a metabolic liver injury characterized by excessive deposition of triglycerides (TG) in hepatocytes. It is an umbrella term for a range of liver diseases, including non-alcoholic fatty liver (NAFL), simple fatty liver (SFL), non-alcoholic steatohepatitis (NASH), cirrhosis, and hepatocellular carcinoma (HCC) in severe circumstances. With the age of onset of NAFLD progressively decreasing and its relationship with cancer risk, research on NAFLD has become even more urgent.

The two-hit hypothesis was initially proposed to explain the pathogenesis of NAFLD, implying that a second strike of other causative factors needs to be involved in the development from simple hepatic steatosis to NASH. Nevertheless, this hypothesis is gradually being revised as new theories emerge. Indeed, various factors, including genetics, dietary habits, air pollution, alcohol, smoking, and insulin resistance, influence the development of NAFLD. Notably, oral health, such as periodontitis, has been reported to be linked to the development of NAFLD. With an evolving understanding of the pathogenesis of NAFLD, its terminology has shifted to MASLD, whilst that of NASH was redefined as metabolic dysfunction-associated steatohepatitis (MASH). Given the correlation between MASLD and metabolic syndrome, it often coexists with metabolic disorders. At the same time, MASLD involves multiple pathogenic molecular pathways, thus leading to heterogeneity in its pathogenesis and clinical manifestations. Based on these findings, a new theory is proposed referring to conditions beyond normal hepatic metabolic capacity, excessive deposition of toxic lipids, hepatocellular stress, injury, and death. The intricate molecular mechanisms underlying MASLD are gradually elucidated. For instance, transmembrane 6 superfamily member 2 (TM6SF2) plays a key role in MASLD, and participates in the regulation of lipid metabolic processes. Nevertheless, there is still no clinically recognized agent for the treatment of MASLD. Therefore, there is an urgent need for further exploration of its pathogenesis. Herein, we aim to conclude molecular mechanisms of MASLD, thus laying a theoretical reference for subsequent diagnostic and therapeutic development.

The pathogenesis of MASLD

Risk factors for MASLD include obesity, insulin resistance, hypertension, and hypertriglyceridemia (Fig. 1). As anticipated, the global prevalence of MASLD increases in parallel with global obesity rates. A meta-analysis documented a prevalence of MASLD of 75.27% in the obese population. Disorders of lipid metabolism are the primary cause of fatty liver. MASLD is predominantly hallmarked by triglyceride accumulation in hepatocytes. Earlier studies have established that a reduction in the level of triglyceride lipase could effectively lower the risk of high-fat diet-induced MASH in mice. While the majority of MASLD patients are obese adults, its incidence in leaner individuals is on the rise, leading to its designation as “lean liver disease”.

Hepatic steatosis can induce oxidative stress, organelle dysfunction, apoptosis, and other pathophysiological changes, thereby promoting the progression of MASLD to MASH and liver fibrosis. Steatosis is the result of caloric overload and the accumulation of large amounts of triglycerides in hepatocytes. The metabolism of free fatty acids (FFA), substrates for TG formation, is of particular importance in this process. The hepatic pathway for fatty acid acquisition encompasses exogenous dietary intake, as well as de novo lipogenesis (DNL). Numerous studies have described that the fatty acids (FAs) are tightly regulated in tissue despite fluctuations in FFA intake. Consequently, increasing FFA intake will not significantly affect its concentration in tissue, but prolonged intake exceeding 10% of total energy can have detrimental effects on health. The close association between the liver and adipose tissue is related to the uptake and synthesis of lipids in the liver. FAs are released into the bloodstream from adipose tissue and transported to the liver bound to plasma proteins. Membrane-bound fatty acid transport proteins (FATPs), namely FATP2 and FATP5, which have been identified in the liver, facilitate the uptake of fatty acids and make them available for hepatic lipid metabolism. According to earlier studies, deficiency of FATPs mitigated the accumulation of hepatic FAs in a high-fat model of mice, demonstrating the promising role of FATPs during hepatic steatosis.

The level of the fatty acid translocase CD36 is increased on the plasma membrane of hepatocytes of MASH patients, while inhibition of CD36 palmitoylation ameliorates intracellular lipid accumulation, providing a viable therapeutic strategy for the treatment of MASLD. Moreover, the levels of two key enzymes in DNL, acetyl-CoA carboxylase (ACC) and fatty acid synthase (FAS), are elevated in MASLD patients, implying that DNL plays an essential role in lipid deposition. Although the mechanisms underlying the activation of DNL in MASLD remain to be elucidated, dysregulation of DNL is considered crucial for fatty liver formation. Increased fatty acid oxidation does not eliminate hepatic lipid deposits but induces dysfunctional mitochondria to produce excessive ROS, thereby contributing to oxidative stress and leading to the development of liver disease. Elevated levels of triglycerides in circulation facilitate FFA infiltration into non-fat tissues, leading to abnormal accumulation of fat and dysfunction of non-fat cells. Recently, the concept of lipotoxicity was introduced. Lipotoxicity drives hepatocyte death by activating inflammatory pathways.

As previously mentioned, the precise mechanisms underlying MASLD remain to be elucidated. This article focused on organelle dysfunction related to hepatocyte injury in the progression of MASLD. The concept of lipotoxicity has been proposed as one of the driving factors leading to MASH, which causes dysregulation of hepatic lipid metabolism and, thus, hepatocellular damage. Enhanced lipotoxicity results in substantial hepatocyte damage via endoplasmic reticulum (ER) stress, activation of inflammatory vesicles, and cell death (Fig. 1). Meanwhile, ferroptosis and gut microbial dysbiosis have also emerged as research hotspots in recent years for exploring the underlying mechanisms of MASLD pathogenesis.

ER stress

As is documented, the unfolded protein response (UPR) refers to a defensive response that maintains the dynamic homeostasis of the endoplasmic reticulum environment, but its prolonged activation induces apoptotic pathways that ultimately cause hepatocyte damage and death. Under different stressful conditions, molecular chaperones undergo ectopic translocation, phosphorylating the three ER receptors and subsequently activating the immunoglobulin-regulated enhancer 1 (IRE1), protein kinase RNA-like endoplasmic reticulum kinase (PERK) or activating transcription factor 6 (ATF6) signaling pathways. Previous studies have reported that ATF6α, PERK/eukaryotic initiation factor-2α (eIF2α), and IRE1α/X-box binding protein 1(XBP1), three ER stress sensing pathways, can regulate the development of MASLD by altering lipid synthesis. Similarly, all three pathways promote the synthesis of C/EBP-homologous protein (CHOP) and directly affect ER stress. The down-regulated expression of GRP78, IRE1α, XBP1, phosphorylated eIF2α, CHOP, and ATF6 attenuates inflammation and HFD-induced ER stress. Salubrinal regulates lipid metabolism and down-regulates CHOP expression via the eIF2α signaling pathway to alleviate lipid accumulation in the liver, providing strategies to mitigate MASLD. Narjes et al. demonstrated that the administration of empagliflozin for five weeks reduced hepatocyte apoptosis and relieved MASLD in HFD-fed mice. Meanwhile, a newly discovered traditional Chinese medicine, Berberine, effectively inhibited PERK-ATF4-CHOP pathway in mouse hepatocytes and macrophages but did not affect ATF6, IRE1α, and GRP78 protein levels. Valdecoxib (VAL), a COX-2 inhibitor, was reported to alleviate lipid accumulation in hepatocytes, and this protective effect was dependent on reduction of ER stress. Therefore, modulating hepatic ER stress represents an effective approach for the treatment of MASLD.

Overall, ER stress remains a popular topic for exploring the pathogenesis of MASLD, wherein CHOP plays a critical role (Fig. 2). Moreover, molecules like XBP1 are also closely related to URP activation and constitute a potential novel target for suppressing ER stress. A growing body of evidence has acknowledged the important role of maladaptive UPR in the progression of liver disease. Therefore, future research may focus on liver-specific ER stress modulators. Additionally, studies with IRE1 and ATF6 in MASLD are warranted to determine the effects of IRE1 or ATF6 inhibitors on MASLD and to identify new targeted drugs for this scenario.

B-cell lymphoma-2(Bcl-2) family proteins and apoptosis

Saturated fatty acids induce apoptosis in hepatocytes (Fig. 2) through the up-regulation of Bcl2-associated x (Bax) and Bcl-2 interacting mediator (Bim) of cell death in the c-Jun N-terminal kinase (JNK)-a dependent pathway and upregulation of the BH3-only protein (bcl-2 homolog3r domain only proteins). P53-up-regulated modulator of apoptosis (PUMA) has also been detected in human samples and animal models with MASH. Upregulation of hepatic PUMA expression is governed by JNK1 and CHOP transcription. The pro-apoptotic protein PUMA interacts with Bax to mediate mitochondrial apoptosis and mobilize caspase activity, which is strongly associated with the progression of MASLD and MASH. In addition, Bim likewise contributes to adipocyte apoptosis and interacts with PUMA to mediate palmitate-induced hepatocytotoxicity. Thus, the deficiency of Bim and PUMA in hepatocytes might alleviate apoptosis and provide a promising direction for the development of MASLD. Prior experiments have demonstrated that the JNK inhibitor JM-2 attenuated adipocyte apoptosis and MASLD by limiting palmitic acid (PA)-induced liver fibrosis and lipid metabolism. Tamoxifen was found to inhibit hepatic fat accumulation by mediating the JNK/MARK signaling pathway, suggesting potential implications for MASLD treatment. At the same time, the protein expression levels of anti-apoptotic such as Mcl-1, which comprises four BH structural domains, were reduced in FFA-exposed hepatocytes. Fernando J et al. revealed that FFA regulates Bim expression by activating FoxO3a and proposed a strategy for the potential treatment of MASH. Cellular Keap1 protein responds to PA-induced hepatotoxicity by undergoing degradation via the p62-dependent autophagy pathway to activate Bim and PUMA, triggering apoptotis. Activation of the pro-apoptotic protein Bax results in cell death by altering mitochondrial membrane permeability and stimulating the caspase response. Given that the level of cytokeratin fragments produced by caspase catabolism serves as a marker in the development of MASLD, caspase inhibitors are a prospective treatment direction. Various caspase inhibitors (Q-VD-OPh, Belnacasan/VX765) have been pioneered, offering candidate therapeutic strategies for MASLD. An aldose reductase inhibitor, epalrestat, acts as the upstream of caspase-1 to inhibit NLRP3 inflammatory vesicles and ameliorate MASH pathology. Recently, Elodie Bosc et al. presented a definitive perspective on caspase-2-specific inhibitors for the treatment of MASLD, while their studies exposed that 3-(S)-neopentyl proline (LJ3a) and 6-methyl-tetrahydro-isoquinoline (LJ2a) inhibited caspase-2-mediated activation of SREBP2.

Taken together, hepatic apoptosis induced by caspases, Bcl-2 family proteins, and c-Jun N-terminal kinase has an impact on influences MASLD/MASH activation. Multiple apoptosis inhibitors have been identified as potential treatments for MASH. Several clinical trials targeting apoptosis in MASH patients are currently ongoing and are expected to be an attractive field for mitigating the progression of MASLD in the future.

Mitochondrial disorder

Bedair Dewidar et al. constructed a MASLD mouse model and measured its mitochondrial respiration. The findings showed that hepatic mitochondrial respiration increased due to fatty acid oxidation (FAO)-driven adaptation to metabolic disorders in response to alterations in lipid metabolism, systemic oxidative stress, and other changes. Interestingly, MASH patients, on the other hand, exhibit increased mitochondrial uncoupling and leakage activity, structural defects, and decreased function, leading to excessive oxidative stress in the liver. Voltage-dependent anion channel (VDAC) acts as an early sensor of lipotoxicity. In response to lipid accumulation, VDAC exhibits a reduction in GSK3-mediated phosphorylation, modulating the permeability of the outer mitochondrial membrane. This allows a large influx of water and calcium into the mitochondria, leading to organelle edema as well as the release of cyt C that eventually induces cell death. Furthermore, in PA-mediated lipotoxicity, the mitochondrial protein Sab interacts with JNK, leading to impairment of the mitochondrial electron respiratory chain, increased ROS production, and ultimately activation of apoptosis. Mitochondrial autophagy eliminates ROS to maintain mitochondrial homeostasis and holds significant implications for the treatment of MASLD. At the same time, excessive intake of SFAs affects the structure and function of hepatic mitochondria and limits respiratory efficiency, which induces liver damage. Additionally, cAMP-response element binding protein H (CREBH), which specifically regulates hepatic lipid metabolism, has been implied as a therapeutic target for hepatocyte resistance to mitochondrial oxidative stress and inflammation in MASH.

Collectively, the previous study demonstrated that SFA plays a vital role in the progression of hepatic steatosis as well as MASLD by impacting the regulation of mitochondrial function. A large number of studies conducted in mice and humans have determined that mitochondrial respiration is typically increased in the early stages of hepatic steatosis. However, this role of mitochondrial respiration in bioenergetics remains underexplored, and there is growing evidence that reactive oxygen species and lipid peroxidation are generated in patients with hepatic steatosis, thereby impairing the respiratory chain and inducing apoptosis. This culminates in a vicious cycle in which massive ROS production exacerbates apoptosis. Although a link between apoptosis stimulated by mitochondrial dysfunction and MASLD has been proposed, further research is necessitated to determine the mechanisms by which SFA regulates mitochondrial respiration, electron leakage, and other pathways that may play a role in the initiation of apoptotic processes.

Lysosomal dysfunction

Studies have uncovered that the relative absence of lysosomal acid lipase in the liver of patients with MASLD reflects lysosomal dysfunction. Of note, damaged autophagy in MASLD is caused by defective lysosomal acidification and lysosomal calcium retention. FFA contributes to the translocation of Bax to lysosomes in hepatocytes, rendering lysosomes unstable and releasing cathepsin B (ctsb) into the cytoplasm, thereby mediating lipotoxicity. Autophagy refers to the mechanism responsible for removing dysfunctional intracellular components through lysosomal degradation and has been shown to mediate intracellular lipid metabolism, a phenomenon termed lipophagy. Recently, Karla K. Frietze et al. unveiled that DDX58 deficiency impairs autophagy and that DDX58 overexpression prevents PA-induced death, indicating that autophagy is a new direction for the treatment of MASLD. At the same time, Liu et al. concluded that autophagy inhibition could be regarded as a potential contributor to MASLD and highlighted the potential of Nrf2, an anti-oxidative stress transcription factor, for the treatment of fatty liver disease. Previous studies have also reported that unsaturated fatty acids exert a protective effect on organelle dysfunction induced by saturated fatty acids. Liu et al.‘s study further demonstrated that oleic acid (OA) supplementation attenuated lysosomal dysfunction caused by disrupted autophagy, presenting OA as a therapeutic agent for metabolic diseases, including MASLD. Of note, cholesterol from dead hepatocytes induces macrophage lysosomal dysfunction, thereby promoting the occurrence of MASH.

Ferroptosis in MASLD

Ferroptosis, first introduced by Stockwell’s work, is an iron-dependent type of non-apoptotic cell death. It is driven by the accumulation of lipid peroxides, unlike the universal forms of cell death (autophagy, apoptosis, and necrosis). Several studies have corroborated that ferroptosis exhibits unique morphological, biochemical, and genetic features. In terms of cellular morphology, ferroptosis is characterized by smaller mitochondrial volume, increased membrane density, and a lower number of cristae, along with insignificant changes in the nucleus. Biochemically, it is usually accompanied by increased lipid peroxidation, elevated ROS levels, and related genetic changes. The regulation of ferroptosis is closely linked to a wide range of metabolisms. Consequently, mounting evidence emphasizes the close relationship between ferroptosis and liver metabolic diseases, including MASLD. Given the relevance of ferroptosis to MASLD, understanding and elucidating the exact pathogenesis of ferroptosis in affecting MASLD is significant. In other words, such insights may contribute to the development and application of potential therapeutic target drugs for MASLD in the future.

Considering the susceptibility of the liver to iron metabolism and lipid peroxidation, a substantial body of evidence supports the notion that ferroptosis may be closely associated with the pathogenesis of MASLD. Li et al. conducted RNA-seq analysis and revealed that ferroptosis was promoted by arachidonic acid metabolism in a methionine-choline deficient (MCD)-diet induced MASH mouse model, suggesting that ferroptosis may be a therapeutic target for MASH. The role of ferroptosis as a trigger for eliciting inflammation in MASH was noted in a study carried out in 2019. Although the underlying mechanisms of ferroptosis in MASLD remain enigmatic, research on ferroptosis has remained vigorous in recent years. Tong et al. observed that the ferroptosis inhibitor liproxstatin-1 restricted hepatocyte apoptosis, pyroptosis, and necroptosis in a mouse model of MAFLD. In addition, Liu et al. documented the antioxidative and anti-inflammatory effects of zeaxanthin (ZAF), an inhibitor of ferroptosis, in FFA-induced HepG2 cells. Most ferroptosis inhibitors can alleviate liver damage and offer possible strategies for intervening in the development of MASLD and inflammation. MASH progression is regulated by numerous ferroptosis-related genes. Among them, GPX4 and Nrf2 stand out as protective mechanisms that inhibit ferroptosis (Fig. 3). Further study of these genes may be beneficial for MASLD treatment. GPX4 is an essential target in MASH, and up-regulation of GPX4 expression can effectively alleviate hepatic metabolic injury. However, a precise understanding of the genetic modulation of GPX4 is still lacking. Further elucidation of the role of GPX4 in MASH via depletion or overexpression in hepatocytes is required. Thymosin beta 4 (Tβ4) inhibits ferroptosis and optimizes lipid metabolism in HFD-induced MASLD mice by protecting against hepatocyte injury and upregulating GPX4. Zhang et al. identified inhibition of the tripartite motif-containing (TRIM59) family as a possible candidate for MASLD treatment, given that it promotes ferroptosis and lipoatrophy by enhancing GPX4 ubiquitination. Targeted induction of inducible-GPX4 (iGPX4) promotes deleterious ferroptosis under MAFLD conditions, contrary to the effect of canonical-GPX4 (cGPX4). Thus, the conversion of GPX4 isoforms provides new horizons for ferroptosis regulation. Nevertheless, MCD dietary modeling is not a complete substitute for physiologically relevant diets in MASLD, posing limitations on data interpretation on GPX4 isozyme conversion.

Given the complex involvement of multiple metabolic pathways and ambiguity in the mechanisms of MASLD, the role of ferroptosis in the prevention and treatment of MASLD deserves further in-depth investigation. Liproxstatin-1 (LPT1), a ferroptosis inhibitor, significantly inhibits PANoptosis (a combination of apoptosis, pyroptosis, and necroptosis) in MASLD and thus attenuates hepatic lipoatrophy, which is conducive to the prevention and treatment of MASLD. In summary, although ferroptosis inhibitors have shown promise in the treatment of MASLD, long-term safety, and optimal dosing regiments need to be further evaluated. In addition, prospective studies remain a prerequisite prior to performing clinical trials.

Gut microbial dysbiosis in MASLD

Gut microbes (GM) play a pivotal role in metabolic homeostasis, and disruptions in gut microbial homeostasis can lead to the development of a variety of metabolic disorders, including MASLD. Dysbiosis of the intestinal flora may increase the permeability of the intestinal barrier, which leads to enhanced absorption of fatty acids. On the other hand, intestinal damage may induce liver damage by exposing the liver to bacteria and their products, such as endotoxins. GM can also chemically modify bile acids (BA) and affect glucose and lipid metabolism in the liver by modulating the BA signaling pathway, thereby influencing the pathogenesis of MASLD. Observations from several studies indicate that the diversity of gut microflora is generally lower in MASLD patients than in the healthy population. Abundance of Gram-negative bacteria (e.g., Bacteroidetes) is enriched, while abundance of Prevotella is lower. Mbaye et al. identified a potential association between lactic acid bacteria and MASH by statistically analyzing the microflora of 10 MASH patient cases and controls. It is universally recognized that gut microbial metabolites play a key role in regulating MASLD pathogenesis. Treatment using Lingguizhugan decoction (a traditional Chinese medicine prescription) for four weeks effectively ameliorated MCD-induced MASH features and reversed the alterations in the abundance of 57 gut microbial metabolites, suggesting the potential of gut flora and its metabolites as therapeutic MASH targets. Short-chain fatty acids (SCFAs), as one of the most common products of carbohydrates (CHOs) and proteins, exerts an integral positive effect in MASLD. Furthermore, clinical evidence demonstrated that SCFA levels are significantly lower in patients with MASH. For example, recent studies have evinced that commensal microbe-derived acetate moderates the development of MASLD through the free fatty acid receptor 2 (FFAR2) signaling pathway in mouse models. In addition, ethanol, an essential gut microbial metabolite, is also strongly associated with MASLD. The role of microbial-derived ethanol in the pathogenesis of MASLD warrants further investigation. By intervening with the selective alcohol dehydrogenase (ADH) inhibitor 4-methyl pyrazole in MASH patients and controls, Meijnikman et al. demonstrated that the elevated ethanol production in patients with MASLD may be driven by the gut microbiome. Elevated levels of alcohol-producing bacteria in the gut and blood ethanol concentrations have been detected in MASH patients, compared to those with hepatic steatosis, indicating that endogenous alcohol could be implicated in the pathogenesis of MASLD. The role of lipid factors in the complex mechanisms of MASLD cannot be overlooked, and recent discoveries suggest potential interactions with gut microbiota homeostasis, offering promising therapeutic directions for delaying MASLD progression. Apelin (APLN) has been hypothesized to be associated with MASLD progression and the gut microbiota, particularly associated with the abundance of Enterobactericae, Prevotellaceae, and Lactobacillaceae. Therefore, changing Apelin levels by altering the gut microbiota may be an effective approach to preventing the progression of MASLD. At present, modulation of gastrointestinal microbiota has been widely studied and applied as a novel target for the treatment of MASLD. Recent studies have found that alanyl-glutamine (AG), a dipeptide comprising alanine and glutamine, can alleviate HFD-induced MASLD by modulating gut microbial composition. The recent discovery that Oat beta-glucan regulates the gut microbiota, and mitigates hepatic inflammation and fibrosis in MASLD, indicating a well-tolerated approach to preventing MASLD. In addition, Liu et al. explored interplay of apolipoprotein H (APOH) and gut microbiota in MASLD. They concluded that down-regulation of APOH induces gut microbial disorders and exacerbates fatty liver, highlighting the role of APOH in fatty liver. Notably, oral health, such as periodontitis, has been theorized to be linked to the development of MASLD. In addition, emerging evidence suggests a relationship between oral and gut microorganisms. The oral-gut-liver axis concept has been proposed, portraying periodontal treatment as a potential treatment and prevention strategy for MASLD. Psoriasis, a prevalent dermatological disease affecting 125 million people worldwide, is closely related to liver disease due to systemic inflammation, as evidenced in various studies. Furthermore, beyond the chronic inflammatory status, intestinal dysbiosis exacerbates the pathogenesis of psoriasis-like phenotypes through fluctuations in fatty acid metabolism. On the other hand, the microbiome plays a critical role in preserving the homeostasis of T cells and immunoglobulin A production in the gastrointestinal tract. At present, the causal relationship between specific intestinal flora and MASLD has not been fully elucidated. Further exploration is required to determine the impact of regulating the intestinal flora and metabolites as a therapeutic strategy for MASLD in the future.

Research prospects for therapeutic strategies

At present, no licensed pharmacological therapy has been approved for the treatment of MASLD, and drug development in MASLD trials remains challenging due to the high variability in histopathological assessment of liver biopsies. Nevertheless, research into treatment options for MASLD is underway, and this review aims to summarize current treatment advances to lay a theoretical reference for future studies.

A healthy diet combined with regular exercise remains the first-line non-pharmacological intervention for the treatment of MASLD. A meta-analysis conducted by Shirin Hassani Zadeh et al. determined that the Mediterranean dietary (MD) pattern reduced the risk of MASLD by 23% compared to the Western dietary pattern. Therefore, lowering ketosis and free fatty acid intake and controlling carbohydrate consumption enhances hepatic metabolic function and reduces the risk of liver disease, thereby preventing the development of MASLD. In addition, the ketogenic diet is involved in controlling MASLD by altering the functional state of liver mitochondria, promoting ketogenesis, and improving hepatic fat metabolism. However, the precise mechanisms of ketosis in MASLD remains unknown. Li et al. explored the therapeutic effects of diet in MASLD patients and determined that intermittent fasting (IF) was more beneficial in reducing the lipotoxicity of MASLD compared to conventional therapies than switching to a normal diet (ND). Recently, a high-fat/high-fructose diet including 10% of bean leaves has also been found to ameliorate lipoatrophy and lipid peroxidation in fatty liver disease, providing new perspectives for the prevention and treatment of MASLD and MASH. Regular exercise may also alleviate glycolipid metabolism disorders and thus be effective against MASLD, but there is no clear evidence regarding the therapeutic effects of exercise modalities in patients with MASLD in the literature.

Although weight loss, dietary modifications, and exercise are recommended for the prevention and treatment of MASLD, they are not a long-term solution, necessitating additional research on effective therapeutic agents for MASLD. The guidance in 2018 stated that omega-3 fatty acids may be effective in MASLD. There have been several subsequent studies addressing the benefits of omega-3 fatty in the treatment of MASLD, among which Mohammad Mohammadi et al. identified the potential synergistic efficacy of fish oils (FOs) and chicory acid (CA) in reducing hepatic fat accumulation in a MASLD in vitro model. Ascribed to the unclear pathogenesis of MASLD, targeted drugs for MASLD have not yet been developed. However, the prevalence of MASLD is statistically higher in T2DM patients; consequently, anti-T2DM drugs such as sodium-glucose cotransporter2 inhibitors, biguanides, and thiazolidinediones are often employed for the treatment of MASLD in the clinical setting. Noteworthily, insulin resistance plays a central role in obesity-related MASLD. It is reported that gremlin-1, a novel secreted insulin antagonist, facilitates MAFLD development according to in vivo and in vitro observation. This effects were accompanied by elevated ER stress and inhibition of autophagy pathway. Resveratrol effectively decreases the levels of fatty liver biomarkers and confers protection against MASLD in animal studies. Nonetheless, further studies are needed to determine its clinical applicability. Breviscapine directly inhibits the TGF-β-activated kinase 1 (TAK1) and is deemed a possible candidate for the treatment of MASH. In recent years, the effect of gut microbes on MASLD has been a research hotspot. Prebiotics and probiotics are considered reasonable options for the prevention and treatment of MASLD. The gut microbiota participates in intestinal energy metabolism, and their implication in the pathogenesis of obesity and MASLD is being increasingly recognized. Similarly, intestinal hormone pathways are potential therapeutic targets for the management of MASLD. Newly identified targeted drugs like PPAR agonists, FXR agonists, and THR-β agonists are currently being investigated in clinical trials and are anticipated to be applied for the treatment of MASLD. To date, bariatric surgery can effectively control obesity and reduce prevalence of MASLD. In addition, the possibility that bariatric surgery induces microbiome alterations and thus prevents MASLD cannot be excluded, a concept that holds promise for the development of novel therapeutic strategies.

Strengths and limitations

This article focuses on the major pathogenic mechanisms of MASLD, including recent research advances in lipotoxicity and gastrointestinal microbiology, as well as possible therapeutic approaches and emerging targets for the treatment of MASLD. Moreover, the article offers a comprehensive overview of the latest research results on MASLD. Nevertheless, there are certain shortcomings that merit acknowledgment. Attributed to data limitations, the provision of clinical trial results on drugs for the treatment of MASLD is relatively lacking. In addition, the bidirectional relationship between pathogenesis and MASLD was not explored in this article. Finally, more research is necessitated to elucidate the intricate links between various mechanisms and the development of MASLD.

Conclusion and outlook

The term MASLD encompasses a spectrum of liver diseases. Among them, MASH, which is featured as inflammation, steatosis, and cellular damage, can lead to liver fibrosis, cirrhosis, and hepatocellular carcinoma. Instead of the conventional two-hit doctrine, the multiple-hit theory is widely accepted, attributing the complex pathogenesis of MASLD to factors such as genetic susceptibility, epigenetic changes, signaling pathways related to hepatic lipid metabolism pathways, and dysbiosis of intestinal microflora. Excessive energy is stored in the body in the form of fatty acids, which are deposited in the liver through fat mobilization and DNL from substrates such as amino acids. Evidently, disturbances in fatty acid metabolism promote hepatic lipid deposition, and the resulting metabolite-induced lipotoxicity strikingly affects MASLD development(Fig. 4). Although MASLD has become a global health concern, pharmacological interventions for its treatment are in the developmental stage. So far, lifestyle interventions remain fundamental to the prevention and treatment of MASLD, with antidiabetic drugs as well as lipid-lowering drugs playing a complementary role. Research into the dysfunction of metabolism remains a key focus for pharmaceutical development, and the influence of gut microbes on MASLD is of interest as a potential therapeutic strategy (Fig. 4). Considering the global prevalence of MASLD and the relatively young age of disease onset, healthcare providers should be more vigilant in timely diagnosing the disease. Likewise, regular medical check-ups are essential for early disease diagnosis and prevention prior to the development of complications.

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    Zhu X, Cai J, Wang Y, Liu X, Chen X, Wang H, et al. A high-Fat Diet increases the characteristics of Gut Microbial Composition and the Intestinal Damage Associated with non-alcoholic fatty liver disease. Int J Mol Sci. 2023.

    Not in our library10.3390/ijms242316733

  17. 17.
  18. 18.

    Luo F, Oldoni F, Das A. TM6SF2: a Novel Genetic Player in nonalcoholic fatty liver and Cardiovascular Disease. Hepatol Commun. 2022;6:448-60.

    Not in our library10.1002/hep4.1822

  19. 19.
  20. 20.

    Quek J, Chan KE, Wong ZY, Tan C, Tan B, Lim WH, et al. Global prevalence of non-alcoholic fatty liver disease and non-alcoholic steatohepatitis in the overweight and obese population: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol. 2023;8:20-30.

    Not in our library10.1016/s2468-1253(22)00317-x

  21. 21.

    Fuchs CD, Radun R, Dixon ED, Mlitz V, Timelthaler G, Halilbasic E, et al. Hepatocyte-specific deletion of adipose triglyceride lipase (adipose triglyceride lipase/patatin-like phospholipase domain containing 2) ameliorates dietary induced steatohepatitis in mice. Hepatology (Baltimore MD). 2022;75:125-39.

    Not in our library10.1002/hep.32112

  22. 22.
  23. 23.

    Hydes T, Alam U, Cuthbertson DJ. The impact of Macronutrient Intake on non-alcoholic fatty liver Disease (NAFLD): too much Fat, too much carbohydrate, or just too many calories? Front Nutr. 2021;8640557. 10.3389/fnut.2021.640557.

    Not in our library10.3389/fnut.2021.640557

  24. 24.

    Marangoni F, Galli C, Ghiselli A, Lercker G, La Vecchia C, Maffeis C, et al. Palm oil and human health. Int J Food Sci Nutr. 2017;68:643-55.

    Not in our library10.1080/09637486.2016.1278431

  25. 25.

    Pohl J, Ring A, Hermann T, Stremmel W. Role of FATP in parenchymal cell fatty acid uptake. Biochim Biophys Acta. 2004;1686:1-6.

    Not in our library10.1016/j.bbalip.2004.06.004

  26. 26.
  27. 27.

    Zhao L, Zhang C, Luo X, Wang P, Zhou W, Zhong S, et al. CD36 palmitoylation disrupts free fatty acid metabolism and promotes tissue inflammation in non-alcoholic steatohepatitis. J Hepatol. 2018;69:705-17.

    Not in our library10.1016/j.jhep.2018.04.006

  28. 28.

    Simões ICM, Amorim R, Teixeira J, Karkucinska-Wieckowska A, Carvalho A, Pereira SP, et al. The alterations of mitochondrial function during NAFLD Progression-An Independent Effect of mitochondrial ROS production. Int J Mol Sci. 2021.

    Not in our library10.3390/ijms22136848

  29. 29.

    Mota M, Banini BA, Cazanave SC, Sanyal AJ. Molecular mechanisms of lipotoxicity and glucotoxicity in nonalcoholic fatty liver disease. Metabolism. 2016;65:1049-61.

    Not in our library10.1016/j.metabol.2016.02.014

  30. 30.

    Pereira ENGS, BPd A, Rodrigues KL, Silvares RR, Guimarães FV, Martins CSM, et al. Cholesterol exacerbates the pathophysiology of non-alcoholic steatohepatitis by Upregulating Hypoxia-Inducible factor 1 and modulating Microcirculatory Dysfunction. Nutrients. 2023;15. 10.3390/nu15245034.

    Not in our library10.3390/nu15245034

  31. 31.

    Pham TH, Lee GH, Jin SW, Lee SY, Han EH, Kim ND, et al. Sesamin ameliorates lipotoxicity and lipid accumulation through the activation of the estrogen receptor alpha signaling pathway. Biochem Pharmacol. 2023;216:115768.

    Not in our library10.1016/j.bcp.2023.115768

  32. 32.

    Ajoolabady A, Aslkhodapasandhokmabad H, Libby P, Tuomilehto J, Lip GYH, Penninger JM, et al. Ferritinophagy and ferroptosis in the management of metabolic diseases. Trends Endocrinol Metab. 2021;32:444-62.

    Not in our library10.1016/j.tem.2021.04.010

  33. 33.
  34. 34.

    Hetz C, Zhang K, Kaufman RJ. Mechanisms, regulation and functions of the unfolded protein response. Nat Rev Mol Cell Biol. 2020;21:421-38.

    Not in our library10.1038/s41580-020-0250-z

  35. 35.
  36. 36.

    Ajoolabady A, Kaplowitz N, Lebeaupin C, Kroemer G, Kaufman RJ, Malhi H, et al. Endoplasmic reticulum stress in liver diseases. Hepatology (Baltimore MD). 2023;77:619-39.

    Not in our library10.1002/hep.32562

  37. 37.

    Gelen V, Sengul E, Yildirim S, Cinar İ. The role of GRP78/ATF6/IRE1 and caspase-3/Bax/Bcl2 signaling pathways in the protective effects of gallic acid against cadmium-induced liver damage in rats. Iran J Basic Med Sci. 2023;26:1326-33.

    Not in our library10.22038/ijbms.2023.71343.15525

  38. 38.

    Liu L, Tang L, Luo J-M, Chen S-Y, Yi C-Y, Liu X-M, et al. Activation of the PERK-CHOP signaling pathway during endoplasmic reticulum stress contributes to olanzapine-induced dyslipidemia. Acta Pharmacol Sin. 2024;45:502-16.

    Not in our library10.1038/s41401-023-01180-w

  39. 39.

    Luo Y, Lei Y, Zhou H, Chen Y, Liu H, Jiang J, et al. ARRB1 downregulates acetaminophen-induced hepatoxicity through binding to p-eIF2α to inhibit ER stress signaling. Cell Biol Toxicol. 2024;40:1.

    Not in our library10.1007/s10565-024-09842-z

  40. 40.
  41. 41.
  42. 42.

    Yang L, Yu S, Yang Y, Wu H, Zhang X, Lei Y, et al. Berberine improves liver injury induced glucose and lipid metabolic disorders via alleviating ER stress of hepatocytes and modulating gut microbiota in mice. Bioorg Med Chem. 2021;55:116598.

    Not in our library10.1016/j.bmc.2021.116598

  43. 43.

    Park SY, Cho W, Abd El-Aty AM, Hacimuftuoglu A, Jeong JH, Jung TW. Valdecoxib attenuates lipid-induced hepatic steatosis through autophagy-mediated suppression of endoplasmic reticulum stress. Biochem Pharmacol. 2022;199:115022.

    Not in our library10.1016/j.bcp.2022.115022

  44. 44.

    Kern P, Balzer NR, Blank N, Cygon C, Wunderling K, Bender F, et al. Creld2 function during unfolded protein response is essential for liver metabolism homeostasis. FASEB J. 2021;35:e21939.

    Not in our library10.1096/fj.202002713rr

  45. 45.

    Luo Y, Jiao Q, Chen Y. Targeting endoplasmic reticulum stress-the responder to lipotoxicity and modulator of non-alcoholic fatty liver diseases. Expert Opin Ther Targets. 2022;26:1073-85.

    Not in our library10.1080/14728222.2022.2170780

  46. 46.

    Alkhouri N, Carter-Kent C, Feldstein AE. Apoptosis in nonalcoholic fatty liver disease: diagnostic and therapeutic implications. Expert Rev Gastroenterol Hepatol. 2011;5:201-12.

    Not in our library10.1586/egh.11.6

  47. 47.

    El-Kashef DH, Sewilam HM. Empagliflozin mitigates methotrexate-induced hepatotoxicity: Targeting ASK-1/JNK/Caspase-3 pathway. Int Immunopharmacol. 2023;114:109494.

    Not in our library10.1016/j.intimp.2022.109494

  48. 48.

    Zhao Q, Yu M, Li J, Guo Y, Wang Z, Hu K, et al. GLUD1 inhibits hepatocellular carcinoma progression via ROS-mediated p38/JNK MAPK pathway activation and mitochondrial apoptosis. Discover Oncol. 2024;15:8.

    Not in our library10.1007/s12672-024-00860-1

  49. 49.

    Cazanave SC, Elmi NA, Akazawa Y, Bronk SF, Mott JL, Gores GJ. CHOP and AP-1 cooperatively mediate PUMA expression during lipoapoptosis. Am J Physiol Gastrointest Liver Physiol. 2010;299:G236-G.

    Not in our library10.1152/ajpgi.00091.2010

  50. 50.

    Chen Y, Yan X, Wang T, Deng H, Deng X, Xu F, et al. PNPLA3 148 M/M Is More Susceptible to Palmitic Acid-Induced Endoplasmic Reticulum Stress-Associated Apoptosis in HepG2 Cells. Int J Endocrinol. 2023;2023(2872408). 10.1155/2023/2872408.

    Not in our library10.1155/2023/2872408

  51. 51.

    Cazanave SC, Mott JL, Elmi NA, Bronk SF, Werneburg NW, Akazawa Y, et al. JNK1-dependent PUMA expression contributes to hepatocyte lipoapoptosis. J Biol Chem. 2009;284:26591-602.

    Not in our library10.1074/jbc.m109.022491

  52. 52.

    Kanda T, Matsuoka S, Yamazaki M, Shibata T, Nirei K, Takahashi H, et al. Apoptosis and non-alcoholic fatty liver diseases. World J Gastroenterol. 2018;24:2661-72.

    Not in our library10.3748/wjg.v24.i25.2661

  53. 53.

    Erlacher M, Labi V, Manzl C, Böck G, Tzankov A, Häcker G, et al. Puma cooperates with Bim, the rate-limiting BH3-only protein in cell death during lymphocyte development, in apoptosis induction. J Exp Med. 2006;203:2939-51.

    Not in our library10.1084/jem.20061552

  54. 54.

    Barreyro FJ, Kobayashi S, Bronk SF, Werneburg NW, Malhi H, Gores GJ. Transcriptional regulation of Bim by FoxO3A mediates hepatocyte lipoapoptosis. J Biol Chem. 2007;282:27141-54.

    Not in our library10.1074/jbc.m704391200

  55. 55.

    Jin L, Wang M, Yang B, Ye L, Zhu W, Zhang Q, et al. A small-molecule JNK inhibitor JM-2 attenuates high-fat diet-induced non-alcoholic fatty liver disease in mice. Int Immunopharmacol. 2023;115109587. 10.1016/j.intimp.2022.109587.

    Not in our library10.1016/j.intimp.2022.109587

  56. 56.

    Fang Z, Xu H, Duan J, Ruan B, Liu J, Song P, et al. Short-term tamoxifen administration improves hepatic steatosis and glucose intolerance through JNK/MAPK in mice. Signal Transduct Target Ther. 2023;8:94.

    Not in our library10.1038/s41392-022-01299-y

  57. 57.

    Masuoka HC, Mott J, Bronk SF, Werneburg NW, Akazawa Y, Kaufmann SH, et al. Mcl-1 degradation during hepatocyte lipoapoptosis. J Biol Chem. 2009;284:30039-48.

    Not in our library10.1074/jbc.m109.039545

  58. 58.

    Zhang M-H, Li J, Zhu X-Y, Zhang Y-Q, Ye S-T, Leng Y-R, et al. Physalin B ameliorates nonalcoholic steatohepatitis by stimulating autophagy and NRF2 activation mediated improvement in oxidative stress. Free Radic Biol Med. 2021.

    Not in our library10.1016/j.freeradbiomed.2020.12.020

  59. 59.

    Hao F, Cubero FJ, Ramadori P, Liao L, Haas U, Lambertz D, et al. Inhibition of Caspase-8 does not protect from alcohol-induced liver apoptosis but alleviates alcoholic hepatic steatosis in mice. Cell Death Dis. 2017;8e3152. 10.1038/cddis.2017.532.

    Not in our library10.1038/cddis.2017.532

  60. 60.

    Chauvier D, Ankri S, Charriaut-Marlangue C, Casimir R, Jacotot E. Broad-spectrum caspase inhibitors: from myth to reality? Cell Death Differ. 2007;14:387-91.

    Not in our library10.1038/sj.cdd.4402044

  61. 61.

    Linton SD, Aja T, Armstrong RA, Bai X, Chen L-S, Chen N, et al. First-in-class pan caspase inhibitor developed for the treatment of liver disease. J Med Chem. 2005;48:6779-82.

    Not in our library10.1021/jm050307e

  62. 62.

    Shi W, Xu G, Gao Y, Zhao J, Liu T, Zhao J, et al. Novel role for epalrestat: protecting against NLRP3 inflammasome-driven NASH by targeting aldose reductase. J Transl Med. 2023;21:700.

    Not in our library10.1186/s12967-023-04380-4

  63. 63.

    Bosc E, Anastasie J, Soualmia F, Coric P, Kim JY, Wang LQ, et al. Genuine selective caspase-2 inhibition with new irreversible small peptidomimetics. Cell Death Dis. 2022;13:959.

    Not in our library10.1038/s41419-022-05396-2

  64. 64.

    Dewidar B, Mastrototaro L, Englisch C, Ress C, Granata C, Rohbeck E, et al. Alterations of hepatic energy metabolism in murine models of obesity, diabetes and fatty liver diseases. EBioMedicine. 2023;94:104714.

    Not in our library10.1016/j.ebiom.2023.104714

  65. 65.

    Koliaki C, Szendroedi J, Kaul K, Jelenik T, Nowotny P, Jankowiak F, et al. Adaptation of hepatic mitochondrial function in humans with non-alcoholic fatty liver is lost in Steatohepatitis. Cell Metab. 2015;21:739-46.

    Not in our library10.1016/j.cmet.2015.04.004

  66. 66.

    Greatorex S, Kaur S, Xirouchaki CE, Goh PK, Wiede F, Genders AJ, et al. Mitochondria- and NOX4-dependent antioxidant defense mitigates progression to nonalcoholic steatohepatitis in obesity. J Clin Invest. 2023;134. 10.1172/JCI162533.

    Not in our library10.1172/jci162533

  67. 67.

    Martel C, Allouche M, Esposti DD, Fanelli E, Boursier C, Henry C, et al. Glycogen synthase kinase 3-mediated voltage-dependent anion channel phosphorylation controls outer mitochondrial membrane permeability during lipid accumulation. Hepatology (Baltimore MD). 2013.

    Not in our library10.1002/hep.25967

  68. 68.

    Wei X, Lin L, Yuan Q-Q, Wang X-Y, Zhang Q, Zhang X-M, et al. Bavachin protects against diet-induced hepatic steatosis and obesity in mice. Acta Pharmacol Sin. 2023;44:1416-28.

    Not in our library10.1038/s41401-023-01056-z

  69. 69.

    Win S, Than TA, Le BHA, García-Ruiz C, Fernandez-Checa JC, Kaplowitz N, Sab. Sh3bp5) dependence of JNK mediated inhibition of mitochondrial respiration in palmitic acid induced hepatocyte lipotoxicity. J Hepatol. 2015;62:1367-74.

    Not in our library10.1016/j.jhep.2015.01.032

  70. 70.

    Zhu L, Wu X, Liao R. Mechanism and regulation of mitophagy in nonalcoholic fatty liver disease (NAFLD): a mini-review. Life Sci. 2023;312:121162.

    Not in our library10.1016/j.lfs.2022.121162

  71. 71.

    Meex RCR, Blaak EE. Mitochondrial dysfunction is a key pathway that Links Saturated Fat Intake to the Development and Progression of NAFLD. Mol Nutr Food Res. 2021;65:e1900942.

    Not in our library10.1002/mnfr.201900942

  72. 72.

    Zhang J, Zhao Y, Wang S, Li G, Xu K. CREBH alleviates mitochondrial oxidative stress through SIRT3 mediating deacetylation of MnSOD and suppression of Nlrp3 inflammasome in NASH. Free Radic Biol Med. 2022;190:28-41.

    Not in our library10.1016/j.freeradbiomed.2022.07.018

  73. 73.

    Li S, Dou X, Ning H, Song Q, Wei W, Zhang X, et al. Sirtuin 3 acts as a negative regulator of autophagy dictating hepatocyte susceptibility to lipotoxicity. Hepatology (Baltimore MD). 2017;66:936-52.

    Not in our library10.1002/hep.29229

  74. 74.

    Yanran W, Jung S, Ko KS. Saturated fatty Acid-Induced impairment of hepatic lipid metabolism is worsened by Prohibitin 1 Deficiency in Hepatocytes. J Med Food. 2022;25:845-52.

    Not in our library10.1089/jmf.2022.k.0028

  75. 75.

    Fan L, Gokaltun A, Maggipinto S, Kitagawa Y, Martyn J, Yeh H, et al. Alterations in Cytoskeleton and Mitochondria in the development and reversal of steatosis in human hepatocytes. Cell Mol Gastroenterol Hepatol. 2023;16:243-61.

    Not in our library10.1016/j.jcmgh.2023.04.003

  76. 76.

    Ferrer MD, Reynés C, Monserrat-Mesquida M, Quetglas-Llabrés M, Bouzas C, García S, et al. Polyunsaturated and Saturated Oxylipin plasma levels allow monitoring the non-alcoholic fatty liver disease progression to severe stages. Antioxid (Basel). 2023.

    Not in our library10.3390/antiox12030711

  77. 77.

    Li S, Li X, Chen F, Liu M, Ning L, Yan Y, et al. Nobiletin mitigates hepatocytes death, liver inflammation, and fibrosis in a murine model of NASH through modulating hepatic oxidative stress and mitochondrial dysfunction. J Nutr Biochem. 2022;100108888. 10.1016/j.jnutbio.2021.108888.

    Not in our library10.1016/j.jnutbio.2021.108888

  78. 78.

    Wolff G, Sakurai M, Mhamane A, Troullinaki M, Maida A, Deligiannis IK, et al. Hepatocyte-specific activity of TSC22D4 triggers progressive NAFLD by impairing mitochondrial function. Mol Metab. 2022;60:101487.

    Not in our library10.1016/j.molmet.2022.101487

  79. 79.
  80. 80.

    Tovoli F, Napoli L, Negrini G, D’Addato S, Tozzi G, D’Amico J, et al. A relative Deficiency of lysosomal acid lypase activity characterizes non-alcoholic fatty liver disease. Int J Mol Sci. 2017;18. 10.3390/ijms18061134.

    Not in our library10.3390/ijms18061134

  81. 81.

    Kim KE, Shin HJ, Ju Y, Jung Y, An HS, Lee SJ, et al. Intermittent fasting attenuates metabolic-dysfunction-Associated Steatohepatitis by enhancing the hepatic autophagy-lysosome pathway. Nutrients. 2023.

    Not in our library10.3390/nu15214574

  82. 82.
  83. 83.

    Feldstein AE, Werneburg NW, Canbay A, Guicciardi ME, Bronk SF, Rydzewski R, et al. Free fatty acids promote hepatic lipotoxicity by stimulating TNF-alpha expression via a lysosomal pathway. Hepatology (Baltimore MD). 2004;40:185-94.

    Not in our library10.1002/hep.20283

  84. 84.

    Singh R, Kaushik S, Wang Y, Xiang Y, Novak I, Komatsu M, et al. Autophagy regulates lipid metabolism. Nature. 2009;458:1131-5.

    Not in our library10.1038/nature07976

  85. 85.

    Frietze KK, Brown AM, Das D, Franks RG, Cunningham JL, Hayward M, et al. Lipotoxicity reduces DDX58/Rig-1 expression and activity leading to impaired autophagy and cell death. Autophagy. 2022;18:142-60.

    Not in our library10.1080/15548627.2021.1920818

  86. 86.

    Liu P, Anandhan A, Chen J, Shakya A, Dodson M, Ooi A, et al. Decreased autophagosome biogenesis, reduced NRF2, and enhanced ferroptotic cell death are underlying molecular mechanisms of non-alcoholic fatty liver disease. Redox Biol. 2023;59102570. 10.1016/j.redox.2022.102570.

    Not in our library10.1016/j.redox.2022.102570

  87. 87.

    Liu W, Zhu M, Gong M, Zheng W, Zeng X, Zheng Q, et al. Comparison of the effects of Monounsaturated fatty acids and polyunsaturated fatty acids on liver lipid disorders in obese mice. Nutrients. 2023.

    Not in our library10.3390/nu15143200

  88. 88.

    Liu X, Li X, Su S, Yuan Y, Liu W, Zhu M, et al. Oleic acid improves hepatic lipotoxicity injury by alleviating autophagy dysfunction. Exp Cell Res. 2023;429:113655.

    Not in our library10.1016/j.yexcr.2023.113655

  89. 89.

    Itoh M, Tamura A, Kanai S, Tanaka M, Kanamori Y, Shirakawa I, et al. Lysosomal cholesterol overload in macrophages promotes liver fibrosis in a mouse model of NASH. J Exp Med. 2023.

    Not in our library10.1084/jem.20220681

  90. 90.

    Dixon SJ, Lemberg KM, Lamprecht MR, Skouta R, Zaitsev EM, Gleason CE, et al. Ferroptosis: an iron-dependent form of nonapoptotic cell death. Cell. 2012;149:1060-72.

    Not in our library10.1016/j.cell.2012.03.042

  91. 91.

    Yagoda N, von Rechenberg M, Zaganjor E, Bauer AJ, Yang WS, Fridman DJ, et al. RAS-RAF-MEK-dependent oxidative cell death involving voltage-dependent anion channels. Nature. 2007;447:864-8.

    Not in our library10.1038/nature05859

  92. 92.

    Yang WS, Stockwell BR. Synthetic Lethal Screening identifies compounds Activating Iron-Dependent, nonapoptotic cell death in Oncogenic-RAS-Harboring Cancer cells. Chem Biol. 2008;15:234-45.

    Not in our library10.1016/j.chembiol.2008.02.010

  93. 93.

    Gautheron J, Gores GJ, Rodrigues CMP. Lytic cell death in metabolic liver disease. J Hepatol. 2020;73:394-408.

    Not in our library10.1016/j.jhep.2020.04.001

  94. 94.
  95. 95.

    Zhang Y, Xin L, Xiang M, Shang C, Wang Y, Wang Y, et al. The molecular mechanisms of ferroptosis and its role in cardiovascular disease. Biomed Pharmacother. 2022;145:112423.

    Not in our library10.1016/j.biopha.2021.112423

  96. 96.

    Zhang H, Axinbai M, Zhao Y, Wei J, Qu T, Kong J, et al. Bioinformatics analysis of ferroptosis-related genes and immune cell infiltration in non-alcoholic fatty liver disease. Eur J Med Res. 2023;28:605.

    Not in our library10.1186/s40001-023-01457-0

  97. 97.

    Zhang T, Wang M-Y, Wang G-D, Lv Q-Y, Huang Y-Q, Zhang P, et al. Metformin improves nonalcoholic fatty liver disease in db/db mice by inhibiting ferroptosis. Eur J Pharmacol. 2024;966:176341.

    Not in our library10.1016/j.ejphar.2024.176341

  98. 98.

    Li X, Wang T-X, Huang X, Li Y, Sun T, Zang S, et al. Targeting ferroptosis alleviates methionine-choline deficient (MCD)-diet induced NASH by suppressing liver lipotoxicity. Liver Int. 2020;40:1378-94.

    Not in our library10.1111/liv.14428

  99. 99.

    Qi J, Kim J-W, Zhou Z, Lim C-W, Kim B. Ferroptosis affects the progression of nonalcoholic steatohepatitis via the modulation of lipid peroxidation-mediated cell death in mice. Am J Pathol. 2020;190:68-81.

    Not in our library10.1016/j.ajpath.2019.09.011

  100. 100.
  101. 101.

    Tong J, Lan X-T, Zhang Z, Liu Y, Sun D-Y, Wang X-J, et al. Ferroptosis inhibitor liproxstatin-1 alleviates metabolic dysfunction-associated fatty liver disease in mice: potential involvement of PANoptosis. Acta Pharmacol Sin. 2023;44:1014-28.

    Not in our library10.1038/s41401-022-01010-5

  102. 102.

    Liu H, Yan J, Guan F, Jin Z, Xie J, Wang C, et al. Zeaxanthin prevents ferroptosis by promoting mitochondrial function and inhibiting the p53 pathway in free fatty acid-induced HepG2 cells. Biochim Biophys Acta Mol Cell Biol Lipids. 2023;1868159287. 10.1016/j.bbalip.2023.159287.

    Not in our library10.1016/j.bbalip.2023.159287

  103. 103.

    Zhu Z, Zhang Y, Huang X, Can L, Zhao X, Wang Y, et al. Thymosin beta 4 alleviates non-alcoholic fatty liver by inhibiting ferroptosis via up-regulation of GPX4. Eur J Pharmacol. 2021;908:174351.

    Not in our library10.1016/j.ejphar.2021.174351

  104. 104.

    Zhang J, Xie H, Yao J, Jin W, Pan H, Pan Z, et al. TRIM59 promotes steatosis and ferroptosis in non-alcoholic fatty liver disease via enhancing GPX4 ubiquitination. Hum Cell. 2023;36:209-22.

    Not in our library10.1007/s13577-022-00820-3

  105. 105.

    Liu Y, Chen M. The TRIM family as a potential target for nonalcoholic fatty liver disease. Hum Cell. 2023;36:870-1.

    Not in our library10.1007/s13577-022-00838-7

  106. 106.
  107. 107.

    Fan Y, Pedersen O. Gut microbiota in human metabolic health and disease. Nat Rev Microbiol. 2021;19:55-71.

    Not in our library10.1038/s41579-020-0433-9

  108. 108.

    Wu J, Li Y, Yang P, Fu J, Wang Y. Gut microbiota and vascular diseases: an update. Cardiovasc Innov Appl. 2024.

    Not in our library10.15212/cvia.2023.0090

  109. 109.

    Xie F, Xu H-F, Zhang J, Liu X-N, Kou B-X, Cai M-Y, et al. Dysregulated hepatic lipid metabolism and gut microbiota associated with early-stage NAFLD in ASPP2-deficiency mice. Front Immunol. 2022;13:974872.

    Not in our library10.3389/fimmu.2022.974872

  110. 110.

    Yuan H, Wu X, Wang X, Zhou J-Y, Park S. Microbial Dysbiosis Linked to Metabolic Dysfunction-Associated fatty liver disease in asians: Prevotella copri promotes Lipopolysaccharide Biosynthesis and Network Instability in the Prevotella Enterotype. Int J Mol Sci. 2024.

    Not in our library10.3390/ijms25042183

  111. 111.

    Zhang D, Wang H, Liu A, Wang S, Xu C, Lan K, et al. The chronic consumption of dietary fructose promotes the gut Clostridium species imbalance and bile acid alterations in developing nonalcoholic fatty liver disease. J Nutr Biochem. 2023;121109434. 10.1016/j.jnutbio.2023.109434.

    Not in our library10.1016/j.jnutbio.2023.109434

  112. 112.

    Kapil S, Duseja A, Sharma BK, Singla B, Chakraborti A, Das A, et al. Small intestinal bacterial overgrowth and toll-like receptor signaling in patients with non-alcoholic fatty liver disease. J Gastroenterol Hepatol. 2016;31:213-21.

    Not in our library10.1111/jgh.13058

  113. 113.

    Boursier J, Mueller O, Barret M, Machado M, Fizanne L, Araujo-Perez F, et al. The severity of nonalcoholic fatty liver disease is associated with gut dysbiosis and shift in the metabolic function of the gut microbiota. Hepatology (Baltimore MD). 2016;63:764-75.

    Not in our library10.1002/hep.28356

  114. 114.

    Mbaye B, Wasfy RM, Alou MT, Borentain P, Andrieu C, Caputo A, et al. Limosilactobacillus Fermentum, Lactococcus lactis and thomasclavelia ramosa are enriched and Methanobrevibacter smithii is depleted in patients with non-alcoholic steatohepatitis. Microb Pathog. 2023;180106160. 10.1016/j.micpath.2023.106160.

    Not in our library10.1016/j.micpath.2023.106160

  115. 115.

    Zhu M, Wang X, Wang K, Zhao Z, Dang Y, Ji G, et al. Lingguizhugan decoction improves non-alcoholic steatohepatitis partially by modulating gut microbiota and correlated metabolites. Front Cell Infect Microbiol. 2023;131066053. 10.3389/fcimb.2023.1066053.

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    Zhu L, Baker SS, Gill C, Liu W, Alkhouri R, Baker RD, et al. Characterization of gut microbiomes in nonalcoholic steatohepatitis (NASH) patients: a connection between endogenous alcohol and NASH. Hepatology (Baltimore MD). 2013;57:601-9.

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    Mbaye B, Magdy Wasfy R, Borentain P, Tidjani Alou M, Mottola G, Bossi V, et al. Increased fecal ethanol and enriched ethanol-producing gut bacteria limosilactobacillus fermentum, Enterocloster bolteae, Mediterraneibacter Gnavus and Streptococcus mutans in nonalcoholic steatohepatitis. Front Cell Infect Microbiol. 2023;131279354. 10.3389/fcimb.2023.1279354.

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    Zeng F, Su X, Liang X, Liao M, Zhong H, Xu J, et al. Gut microbiome features and metabolites in non-alcoholic fatty liver disease among community-dwelling middle-aged and older adults. BMC Med. 2024;22:104.

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    Effenberger M, Grander C, Hausmann B, Enrich B, Pjevac P, Zoller H, et al. Apelin and the gut microbiome: potential interaction in human MASLD. Dig Liver Dis. 2023.

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    Zheng Y, Ying H, Shi J, Li L, Zhao Y. Alanyl-Glutamine Dipeptide attenuates non-alcoholic fatty liver Disease Induced by a high-Fat Diet in mice by improving gut microbiota dysbiosis. Nutrients. 2023;15. 10.3390/nu15183988.

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    Jaeger JW, Brandt A, Gui W, Yergaliyev T, Hernández-Arriaga A, Muthu MM, et al. Microbiota modulation by dietary oat beta-glucan prevents steatotic liver disease progression. JHEP Rep. 2024.

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    Liu Y, Zhao Y, Liu Q, Li B, Daniel PV, Chen B, et al. Effects of apolipoprotein H downregulation on lipid metabolism, fatty liver disease, and gut microbiota dysbiosis. J Lipid Res. 2024.

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    Qiao F, Li X, Liu Y, Zhang S, Liu D, Li C. Periodontitis and NAFLD-related diseases: a bidirectional two-sample mendelian randomization study. Oral Dis. 2023.

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    Wang M, Li L, Qian J, Wang N, Bao J, Lu J, et al. Periodontitis salivary microbiota exacerbates nonalcoholic fatty liver disease in high-fat diet-induced obese mice. IScience. 2023;26:106346.

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    Kuraji R, Ye C, Zhao C, Gao L, Martinez A, Miyashita Y, et al. Nisin lantibiotic prevents NAFLD liver steatosis and mitochondrial oxidative stress following periodontal disease by abrogating oral, gut and liver dysbiosis. NPJ Biofilms Microbiomes. 2024.

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    Kamata Y, Kessoku T, Shimizu T, Sato S, Kobayashi T, Kurihashi T, et al. Periodontal Treatment and Usual Care for nonalcoholic fatty liver disease: a Multicenter, Randomized Controlled Trial. Clin Transl Gastroenterol. 2022;13:e00520.

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    Balato N, Napolitano M, Ayala F, Patruno C, Megna M, Tarantino G. Nonalcoholic fatty liver disease, spleen and psoriasis: New aspects of low-grade chronic inflammation. World J Gastroenterol. 2015;21:6892-7.

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    Takezaki D, Morizane S, Ikeda K, Iseki M, Sakamoto Y, Kawakami Y, et al. Co-occurrence of non-alcoholic steatohepatitis exacerbates psoriasis associated with decreased adiponectin expression in a murine model. Front Immunol. 2023;14:1214623.

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    Zhao Q, Yu J, Zhou H, Wang X, Zhang C, Hu J, et al. Intestinal dysbiosis exacerbates the pathogenesis of psoriasis-like phenotype through changes in fatty acid metabolism. Signal Transduct Target Ther. 2023.

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    Huus KE, Petersen C, Finlay BB. Diversity and dynamism of IgA-microbiota interactions. Nat Rev Immunol. 2021;21:514-25.

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    Harrison SA, Allen AM, Dubourg J, Noureddin M, Alkhouri N. Challenges and opportunities in NASH drug development. Nat Med. 2023;29:562-73.

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    Al Hashmi K, Giglio RV, Pantea Stoian A, Patti AM, Al Waili K, Al Rasadi K, et al. Metabolic dysfunction-associated fatty liver disease: current therapeutic strategies. Front Nutr. 2024;11:1355732.

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    Hassani Zadeh S, Mansoori A, Hosseinzadeh M. Relationship between dietary patterns and non-alcoholic fatty liver disease: a systematic review and meta-analysis. J Gastroenterol Hepatol. 2021;36:1470-8.

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    Risi R, Tozzi R, Watanabe M. Beyond weight loss in nonalcoholic fatty liver disease: the role of carbohydrate restriction. Curr Opin Clin Nutr Metab Care. 2021;24:349-53.

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    Luukkonen PK, Dufour S, Lyu K, Zhang X-M, Hakkarainen A, Lehtimäki TE, et al. Effect of a ketogenic diet on hepatic steatosis and hepatic mitochondrial metabolism in nonalcoholic fatty liver disease. Proc Natl Acad Sci U S A. 2020;117:7347-54.

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    Watanabe M, Tozzi R, Risi R, Tuccinardi D, Mariani S, Basciani S, et al. Beneficial effects of the ketogenic diet on nonalcoholic fatty liver disease: a comprehensive review of the literature. Obes Rev. 2020;21:e13024.

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    Li D, Dun Y, Qi D, Ripley-Gonzalez JW, Dong J, Zhou N, et al. Intermittent fasting activates macrophage migration inhibitory factor and alleviates high-fat diet-induced nonalcoholic fatty liver disease. Sci Rep. 2023;13:13068.

    Not in our library10.1038/s41598-023-40373-5

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    Becerril-Campos AA, Ramos-Gómez M, De Ríos-Arellano L, Ocampo-Anguiano EA, González-Gallardo PV, Macotela A. Bean leaves ameliorate lipotoxicity in fatty liver disease. Nutrients. 2023.

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    Fang C, Liu S, Yang W, Zheng G, Zhou F, Gao X, et al. Exercise ameliorates lipid droplet metabolism disorder by the PLIN2-LIPA axis-mediated lipophagy in mouse model of non-alcoholic fatty liver disease. Biochim Biophys Acta Mol Basis Dis. 2024;1870167045. 10.1016/j.bbadis.2024.167045.

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    Qi Z, Le S, Cheng R, Du X, Zhao C, Zhang Z, et al. Responses of the serum lipid Profile to Exercise and Diet interventions in nonalcoholic fatty liver disease. Med Sci Sports Exerc. 2024.

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    Mohammadi M, Abbasalipourkabir R, Ziamajidi N. Fish oil and chicoric acid combination protects better against palmitate-induced lipid accumulation via regulating AMPK-mediated SREBP-1/FAS and PPARα/UCP2 pathways. Arch Physiol Biochem. 2023;129:1-9.

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    He X, Li Y, Deng X, Xiao X, Zeng J. Integrative evidence construction for resveratrol treatment of nonalcoholic fatty liver disease: preclinical and clinical meta-analyses. Front Pharmacol. 2023;14:1230783.

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    Lan T, Jiang S, Zhang J, Weng Q, Yu Y, Li H, et al. Breviscapine alleviates NASH by inhibiting TGF-β-activated kinase 1-dependent signaling. Hepatology (Baltimore MD). 2022;76:155-71.

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    Rodríguez-Pastén A, Fernández-Martínez E, Pérez-Hernández N, Soria-Jasso LE, Cariño-Cortés R. Prebiotics and Probiotics: effects on Dyslipidemia and NAFLD/NASH and the Associated mechanisms of Action. Curr Pharm Biotechnol. 2023;24:633-46.

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    Koukias N, Buzzetti E, Tsochatzis EA. Intestinal hormones, gut microbiota and non-alcoholic fatty liver disease. Minerva Endocrinol. 2017;42:184-94.

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    Dong TS, Katzka W, Yang JC, Chang C, Arias-Jayo N, Lagishetty V, et al. Microbial changes from bariatric surgery alters glucose-dependent insulinotropic polypeptide and prevents fatty liver disease. Gut Microbes. 2023;15:2167170.

    Not in our library10.1080/19490976.2023.2167170

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