The Effect of Probiotics on the Production of Short-Chain Fatty Acids by Human Intestinal Microbiome

1The most attention in research on human microbiome is devoted to the analysis of the diversity of microorganisms present in the digestive system, especially in the intestines. This metagenome is often called the third main mammalian genome, in addition to the nuclear and mitochondrial genomes. Nutrient absorption and energy regulation depend on environmental and lifestyle factors (dietary habits, drug treatments, intestinal motility and stool frequency and consistency) as well as the bacteria commonly found in the gastrointestinal tract (referred to as the intestinal or gut microbiome). Among the about 60 phyla of bacteria currently known, only some are present in human intestines (e.g., Firmicutes, Bacteroides, Actinobacteria, Fusobacteria, Proteobacteria, Verrucomicrobia, Cyanobacteria, and Spirochaetes). Two bacterial phyla, Gram-positive Firmicutes (Lactobacillus spp., Bacillus spp., and Clostridium spp.) and Gram-negative Bacteroidetes, predominate in human gut.

2The type and proportions of microorganisms found in the intestines, i.e., the enterotype may determine the host’s energy balance. In addition, the intestinal microbiome supports the biotransformation of numerous chemical compounds. Due to their metabolic abilities, intestinal microorganisms enable the transformation of complex nutrients, such as plant cell wall components (cellulose, pectin, hemicellulose, lignin) and mucins into simple sugars that are fermented to form short-chain fatty acids (SCFAs, mainly acetate, propionate and butyrate). The intestinal microbiome also plays an important role in modulating mucosal homeostasis of immune cell subpopulations and the synthesis of certain vitamins. The activity of microorganisms in the intestines has a significant effect on the action of gastrointestinal hormones, maintaining intestinal homeostasis, regulates the proliferation and differentiation of epithelial cells, and prevents mucosal colonization by pathogenic microorganisms.

3An imbalance of the intestinal microbiome and a decrease in the number of bacteria producing metabolites such as SCFAs (e.g., acetic, propionic and butyric acid) often occur in patients with inflammatory bowel diseases (IBD), irritable bowel syndrome (IBS), type 2 diabetes (T2D), obesity, autoimmune disorders or in cancer patients. A lower abundance of specific bacteria and SCFAs leading to gut barrier dysfunction, low-grade inflammation and altered glucose, lipid and energy homeostasis are characteristic for obesity and T2D. The composition of the intestinal microbiota was found to be different in people with obesity than in people of normal weight. This is confirmed, among others, by studies in which Faecalibacterium prausnitzii was found to be the most abundant (about 5% of the bacterial population) in the intestines of healthy adults, while overweight people had a higher number of Firmicutes and Actinobacteria and a lower number of Bacteroidetes, Verrucomicrobia and F. prausnitzii. Thus, research results indicate that obesity is associated with a decrease in the number of Bacteroidetes and an increase in the number of Firmicutes, with the intestinal microbiome of an obese person being less diverse than that of a lean person. It should also be noted that Faecalibacterium prausnitzii is the first anti-inflammatory commensal bacterium identified on the basis of human clinical data and is also one of the major butyrate-producer of the human intestinal microbiome. Other studies have shown a higher concentration of SCFAs (especially butyric and propionic acid) in the feces of overweight children compared to healthy children. Similar results were obtained in a study of Swiss children, in this case the concentration of butyric and propionic acid was also significantly higher in the feces of overweight children. However, different results were obtained for overweight Japanese and Mexican children, where SCFAs concentration was higher in the feces of children with normal weight. Therefore, the trend of SCFAs content in feces cannot be dependent on a specific BMI group. Instead, the concentration of these acids is more associated with dysbiosis of the intestinal microbiome, genetics, environmental factors and diet.

4There are many methods for modulating the intestinal microbiome. One of these is the use of probiotics, which can be helpful in maintaining or restoring homeostasis in the intestines to improve human health and prevent many diseases. According to the definition formulated in 2002 by the FAO (Food and Agriculture Organization of the United Nations, Rome, Italy) and the WHO (World Health Organization, Geneva, Switzerland), probiotics are live microorganisms which, when administered in adequate amounts, confer a health benefit on the host. The definition was maintained by the International Scientific Association for Probiotics and Prebiotics (ISAPP) in 2013 and is still currently used. The most commonly used probiotics are lactic acid bacteria (LAB) and bifidobacteria. The growth and metabolic activity of probiotic microorganisms can be selectively stimulated by various types of carbohydrates that are not digested by the host (prebiotics). The combinations of probiotics with prebiotics (called synbiotics) are able to shift the predominant bacteria and the production of SCFAs of fecal microorganisms in a model system of the human colon.

5Organic acids, principally the short-chain fatty acids (SCFAs) are formed in the GI tract in millimolar quantities and especially occur in high amounts in those areas where anaerobic microorganisms are predominant. SCFAs are volatile saturated fatty acids that have in their chain 1-6 carbon atoms in the aliphatic chain, existing in a straight or branched conformation. In this review, attention has been focused on SCFAs with a simple conformation, which include formic, acetic, propionic, butyric, valerian, and caproic acids (Table 1).

6SCFAs represent the main carbon flow from the diet to the host microbiome. The formation of these acids is relatively well-known and described. The concentration and ratio of resulting SCFAs depend not only on the composition of the microbiome and the number of individual microorganisms in the colon, but also on the type of dietary fibers supplied to the microorganisms as a substrate in the fermentation process, and thus on the diet. The most common are acetic acid, propionic acid and butyric acid (in a 3:1:1 molar ratio), which constitute 90%–95% of SCFAs present in the human colon, while a smaller proportion of these is formic acid.

7In addition, the fermentation of selected, often rapidly fermentable non-digestible carbohydrates (NDCs) produces another organic acid-lactic acid. Although it does not belong to the group of SCFAs, this acid can be produced by lactic acid bacteria, e.g., the genera Lactobacillus and Bifidobacterium. However, under normal conditions it is not accumulated in the colon due to the presence of some bacterial species, e.g., Eubacterium hallii, that can convert lactate into different SCFAs. Metagenomic analyses have greatly facilitated the identification of the types of bacteria responsible for the production of SCFAs and lactic acid (Table 2).

8Endogenous short-chain fatty acids are formed by bacterial fermentation of food fiber and NDCs, which become available to intestinal microorganisms in the large intestine. In addition to resistant starch (RS), plant-derived NDCs include non-starch polysaccharides (NSP), oligosaccharides (prebiotics), oligofructose, disaccharides (lactose, stachyose, raffinose) and monosaccharides e.g., alcohols (sorbitol, mannitol). There are four types of resistant starch (RS1–RS4) present in the human diet that are resistant to degradation in the small intestine. The type of RS has a significant effect on the composition of the intestinal microbiome. In the case of oligosaccharides, particularly important are prebiotics defined as a nonviable food component that confers a health benefit on the host associated with modulation of the microbiota. However, endogenous indigestible carbohydrates include mucin and milk oligosaccharides.

9Fermentation is an anaerobic redox process in the cytoplasm in which organic compounds are both electron donors and acceptors. In the fermentation process, electrons detached from the oxidized substrate are transferred by NADH directly to the endogenous acceptor. ATP is formed as a result of substrate phosphorylation, with the participation of the corresponding phosphoglycerate, pyruvate, acetate or butyrate kinases. During carbohydrate fermentation, the final electron acceptor is pyruvate or the compounds that are produced from it. The end products of fermentation are various short chain carboxylic acids (e.g., formic, acetic, lactic, butyric, propionic), CO2, H2, ethanol, glycerol, acetoin, 2,3-butanediol. Importantly, bacterial growth in populations mixed with other microorganisms can affect the type and amount of products produced during fermentation. The substrates most commonly used by microorganisms in the fermentation process are hexoses and pentoses.

10Bacteria have a variety of pathways to transform sugars. These sugars are first phosphorylated and then in glycolysis (Embden–Meyerhof–Parnassian pathway), in the Entner–Doudoroff pathway or in the Bifidobacterium pathway are transformed into pyruvate or into pyruvate and additional acetyl-phosphate. The Embden–Meyerhof–Parnassian pathway, the major colonic pathway for the catabolism of hexoses, occurs in enterobacteria, clostridia, homofermentative lactic acid bacteria, and propionibacteria, and produces only pyruvate as a partial oxidation product). The Entner–Doudoroff pathway is used in the fermentation metabolism by e.g., Zymomonas (alcoholic fermentation), as well as Escherichia coli in gluconate fermentation. The Bifidobacterium pathway is active in bacteria of the genus Bifidobacterium, inhabiting, among others, the human digestive system. Two acetate molecules and one lactate are formed in this pathway. In the phosphoketolase pathway that occurs in heterofermentative lactic acid bacteria or the Bifidobacterium pathway, an additional molecule of acetyl-phosphate is generated (Figure 1).

11In a mixed population such as the intestinal microbiome, carbohydrate breakdown into a mixture of acids involves more than one species. This type of fermentation is called mixed acid fermentation or Enterobacteriaceae fermentation and is carried out by some bacteria belonging to this family, including Escherichia, Proteus, Salmonella, and Shigella. The fermentation products of some species are substrates for fermentation or incorporated as intermediate metabolites into the metabolic pathways of other species, resulting in substrates being sequentially fermented. Lactate, ethanol, and pyruvate are diminished by subsequent bacterial utilization and SCFAs production. Accordingly, the main final products of sugar catabolism are SCFAs, acetate, propionate and butyrate that account for 85%–95% of total SCFAs in all regions of the colon. Other fermentation end products, such as caproate and valerate, occur in lower amounts.

12Acetic acid is the most abundant SCFAs in the colon, accounting for more than half of the total SCFAs found in feces. Intestinal microorganisms can produce acetic acid through two major metabolic processes. Most often it is fermentation of indigestible carbohydrates, while about 1/3 of acetic acid is formed as a result of synthesis from hydrogen and carbon dioxide or formic acid by acetogenic bacteria through the Wood–Ljungdahl pathway.

13Some types of Clostridium (C. acetobutylicum, C. butyricum, C. pasteurianum, C. perfringens) participate in butyric fermentation, as well as e.g., Butyrivibrio fibrisolvens and Fusobacterium nucleatum. The end products are butyric acid, a small amount of acetic acid and CO2 and H2. Some species may also form lactic acid and/or ethanol as well.

14For propionic fermentation, the main substrates are glucose and lactate. Its course varies depending on the bacteria; it can occur that it forms succinate or acrylate.

15Bacteria are capable of fermenting sugar degradation products (glycerol, citrate, malate, succinate, pyruvate, lactate, ethanol, acetate), and a small share of dietary protein fermentation processes in the production of SCFAs has been shown, mainly in the form of acetic and propionic acid. Bacteria of the genus Clostridium are capable of fermenting amino acids. In this process, carbon dioxide, hydrogen, acetate, as well as ammonia and butyrate may form, which have an unpleasant odor. In addition, amino acids such as valine, leucine and isoleucine resulting from the anaerobic breakdown of proteins can be converted into compounds with strong odor, such as isobutyric, isovaleric and hexanoic acids, as well as cadaverine, putrescine, other amines, and hydrogen sulfide and methylmercaptan. Excessive accumulation of isobutyric acid and isovaleric acid indicates a malfunctioning fermentation and digestion processes. These are putrefactive acids, the increased production of which may be associated with an excess of unabsorbed amino acids or proteins reaching the intestines. The possibility of blood in the intestinal contents and the overly intensive development of pathogenic microbiota in the small intestine should also be taken into account, where access to protein compounds is facilitated.

16SCFAs have been shown to have a very positive effect on the energy metabolism of mammals that use them together with glucose as a metabolic fuel. It has been estimated that the use of SCFAs as an energy source can provide up to 10% of the host’s daily calories. The presence of these acids in the human body, mainly acetic, butyric and propionic acids in sufficient quantities is essential for the health and well-being of the host. However, the production of these acids requires the presence of appropriate substrates (dietary fiber and prebiotics) needed for the proper course of the fermentation processes.

17SCFAs play a very important role in maintaining intestinal and immune homeostasis in the human body (Figure 2).

18SCFAs are speculated to have a mediational role in the microbiota–gut–brain axis crosstalk. Two major SCFAs signaling mechanisms have been identified, namely inhibition of HDACs and activation of GPCRs—The binding partners of GPR41 and GPR43 (Table 3).

19SCFAs play a very important role in regulating pH, increasing the absorption of calcium, iron, as well as magnesium, and are beneficial for glucose and protein metabolism in the liver. In addition, these acids affect the maintenance of the normal structure, integrity and function of the intestines. They show anti-inflammatory activity, which involves inhibiting the activity of inflammatory mediators in the intestinal epithelium, and thus inhibiting the activation of NFκB macrophages, which are the main source of cytokines in the course of the inflammatory process of inflammatory bowel diseases. These acids are the primary source of energy for colonocytes. It has been shown that the source of 70% of the energy used by intestinal epithelial cells (IEC) is butyric acid produced by commensal bacteria, especially such as Ruminococcus and Faecalibacterium (Table 4). In addition, by simulating the growth of saprophytic microflora, SCFAs inhibit the development of pathogenic microorganisms such as Escherichia coli, Salmonella, or Campylobacter, competing for colonization sites. Studies have shown that butyric acid stimulates the expression of the MUC2 gene in cell lines and the production of mucin, and the sticky layer it creates protects the intestinal epithelium from contact with toxins and pathogenic microorganisms. In contrast, studies of programmed cell death from a tumor line have demonstrated the effectiveness of butyric acid in inhibiting their development and inducing the process of apoptosis. In addition, butyric acid and propionic, acetic, and valeric acids have been shown to induce apoptosis (Table 4).

20SCFAs increase the amount of mucus produced and the speed of blood flow. More importantly, they provide acetyl-CoA used in the process of fat biosynthesis and cell membrane production, guaranteeing the integrity of mucous membranes. There are indications that SCFAs are key mediators of the beneficial effects of intestinal microbiota. SCFAs also directly modulate host health through a number of tissue-specific mechanisms associated with intestinal barrier function, glucose homeostasis, immunomodulation, appetite regulation, obesity, and have a direct and indirect effect on cardiovascular disease (CVD) risk markers.

21At present, relatively little is known about the function of formic acid in the intestines. There are indications that its presence is associated with methanogenesis and its concentration may be elevated during inflammation (Table 4). Acetic acid concentration in the colon is the highest of all SCFAs, and in cells it is a key factor in the metabolism of carbohydrates and fats. In addition, acetic acid is absorbed by the liver, where it participates in the synthesis of cholesterol (Table 4). Propionic acid is produced in the human gut mainly by Bacteroidetes and Firmicutes. This acid is an inhibitor of gluconeogenesis and cholesterol synthesis in the liver. In addition, it has antibacterial and anti-inflammatory effects, taking part in the protection of human intestines against pathogens. Butyric acid exerts the strongest anti-inflammatory effect of all SCFAs. The cause of the inflammatory process of the intestinal mucosa, which accompanies many pathological processes, is a lack of energy. Butyric acid is the main source of energy for intestinal epithelial cells. Butyric acid has a beneficial immunoregulatory effect on intestinal epithelial cells and other mucosal cell populations. It modulates gene expression by affecting both stimulants and inhibitors of expression. Some of these mechanisms are based on histone hyperacetylation due to inhibition of the histone deacetylase enzyme activity (Table 4).

22Unlike other SCFAs, the role of valeric acid in gut health is not fully understood. In a limited number of studies, it was found that valeric acid can stimulate the growth of intestinal epithelium and have a beneficial effect on the pathogenesis of diseases such as colitis, cardio-metabolic diseases and cancer (Table 4).

23In order to determine the effect of probiotics on the SCFA production to human intestinal microbiome of a literature review was conducted using the database Web of Science, Medline, Elsevier. To identify relevant studies, articles from 1996 to 2020 in databases were searched. The following keywords were used in the search: Probiotic, SCFA, colorectal cancer, obesity, diabetes, type 2 diabetes, atopic dermatitis, autism spectrum disorders, cardiovascular disease, gastrointestinal disorders, etc. The search was restricted to publications in English. A comprehensive full-text review of identified studies was conducted after the title and abstract screening of potentially relevant articles.

24Intestinal microorganisms, due to their participation in metabolic processes, have a significant impact on the metabolism of the whole body. The balance of this microbiome is necessary to maintain the proper health of the host and prevent many diseases. Therefore, researchers hypothesized that in people in whom the number of certain groups of microorganisms is too low, deliberate reproduction or administration of these microorganisms may be beneficial.

25In in vitro human intestinal model studies (the M-SHIME® system), effect of an aqueous probiotic suspension (SymproveTM, containing Lactobacillus acidophilus NCIMB 30175, Lactobacillus plantarum NCIMB 30173, Lactobacillus rhamnosus NCIMB 30174, and Enterococcus faecium NCIMB 30176) on bacterial diversity was tested. SCFAs production and inflammatory markers after 3 weeks dosing of probiotic was found. The results confirmed colonization and growth of three probiotic species in the luminal and mucosal compartments of the proximal and distal colon, and growth of a last species in the luminal proximal colon. The colonization and growth probiotic bacteria leaded to higher proximal and distal colonic lactate concentrations. In effect, the lactate stimulated growth of lactate-consuming bacteria and resulting in increased SCFAs production, especially butyrate. Additionally, an immunomodulatory effect of the probiotics was seen; production of anti-inflammatory cytokines (IL-10 and IL-6) was increased and production of inflammatory chemokines (IL-8, CXCL 10 and MCP-1 and) was reduced.

26In another study, the effect of oral consumption of Lactobacillus plantarum P-8 (Lp-8) on human intestinal microflora, and SCFAs of different aged adults was tested. 33 volunteers including young (mean age 26 years), middle-aged (mean age 51 years), and elderly (mean age 76 years) received Lp-8 (6 × 1010 colony forming units daily) for 4 weeks. The increase in Bifidobacterium and other beneficial bacteria was found, whereas Desulfovibrio and other opportunistic pathogens decreased after taking probiotic for 4 weeks. A statistically significant increase in acetate and propionate levels in all age groups was found, which reached a peak after 5 weeks in all age groups.

27Other scientists also tested the anti-aging potential of a probiotic in combination containing Lactobacillus paracasei ssp. paracasei BCRC 12188, Lactobacillus plantarum BCRC 12251, and Streptococcus thermophilus BCRC13869. The studies used the murine model in vivo, wherein the aging induced d-galactose. The 12-week study was conducted on 15 mice. It turns out that long-term administration of the probiotic mixture by increasing the production of SCFAs (might regulate antioxidant enzymes by inducing expression of Nrf2 or HO-1) and inhibiting cell apoptosis and brain injury, resulting in improved memory and learning abilities in d-galactose–treated aging mice.

28Moreover, in different research the potential health benefits of a fermented salami with a probiotic Lactobacillus rhamnosus HN001 and added citrus fiber for 4 weeks in 24 health people was tested. It was found that the inflammatory markers CRP and TNFα decreased significantly after intervention, suggesting a less inflammatory environment after reformulated salami consumption. In addition, antioxidant plasmatic markers also improved and butyrate production was significantly increased within the intervention group.

29CRC is the third most prevalent cause of death among the different types of cancer and the highest incidence being in developed countries. It is estimated that by 2035, 24.4 million new cases of CRC will be diagnosed annually. CRC is strongly correlated with decreased levels of SCFAs and microbiome dysbiosis. Administration of Butyrivibrio fibrisolvens MDT-1, (known for their high production of butyrate) in mouse model of colon cancer, inhibited progression of tumor development, affecting also the reduction of β-glucuronidase and increasing the immune response. Currently, it is suggested to modulate SCFA-producing bacteria through dietary intervention with fermentable fibers as a possible treatment for CRC. In many in vitro studies have attempted to determine effects and potential mechanisms of action of probiotics in the inhibition of cancer cell proliferation. In the research on human colonic cancer cell line Caco-2, Pediococcus pentosaceus FP3, Lactobacillus salivarius FP25 and FP35, and Enterococcus faecium FP51 in different concentrations were tested. Tested probiotics reduced cell proliferation. Mechanisms responsible for this effect were adhesion of probiotic bacteria to colon cancer cells and an increase in bioproduction of SCFAs. On the other hand, in the study on human colonic cancer cells lines HT-29 and Caco-2 with using skimmed milk kefir and ayran, antioxidant and SCFAs activities were recognized as mechanisms responsible for the beneficial effect of the probiotic. In this case, beneficial effect of probiotics was associated with lowering genotoxicity of fecal water added to the medium. Other studies also confirmed the beneficial effect of SCFAs. In the research on human colonic cancer cells lines HCT116, SW1116, and Caco-2, the effect and the mechanism of action Clostridium butyricum ATCC 23857 and Bacillus subtilis ATCC 19398 were analyzed. A beneficial effect was the reduction of cell proliferation and expression of inflammatory genes as a result of the presence of bacitracin or butyrate in the conditioned medium induced cell cycle arrest and apoptosis activation. In the studies on male rats F344 (5 weeks old) the effect of Lactobacillus salivarius was tested. As a result of the decrease in azoreductase activity and the intestinal population of Bacillus and Ruminococcaceae while increasing the number of intestinal populations of Prevotella, Bacteroides, Lachnospiraceae, Clostridium, and the concentration of SCFAs in feces, a decrease in aberrant crypt foci (ACF) incidence was found. As part of the randomized, double-blind, placebo-controlled research 10 colorectal cancer patients and 20 healthy subjects were receiving Lactobacillus gasseri OLL271 6: LG21 for 12 weeks. The effect of the tested probiotic was increase number of Lactobacillus spp. and decrease number of Clostridium perfringens in intestinal population. Moreover, increase in concentration isobutyric acid in feces and natural killer (NK) cell activity were found. In addition, supplementation of probiotic caused a decrease in pH and the synthesis of fecal putrefaction products (Table 5).

30In another research, effect of Bifidobacterium lactis LAFTI B94 administration in 17 healthy subjects (aged 45 to 75 years) for 4 weeks was tested. The treatment resulted increase number of Bifidobacterium lactis in intestinal population, but changes in the pH, the SFCA fecal concentration, the serum hs-CRP and cytokines and also the crypt proliferation and cell height weren’t found (Table 5).

31Obesity is a risk factor for CVD, dyslipidemia, hepatobiliary disease diabetes, premature death, and several cancers. There is an estimate of 1.7 billion people in the world that are overweight. Individuals with obesity usually have an altered composition of intestinal microbiome, which suggest that intestinal microbiome can be considered the factor that creates the development of obesity. Changes in the composition of the intestinal microbiome can be associated with obesity through changes in the form of reduced activity of the fasting-induced adipose factor (FIAF) and AMP-activated protein kinase (AMK), reduced production of SCFAs, increased inflammation or altered LPS-endocannabinoid (eCB) system regulators loops, and bile acid metabolism. The host’s diet is considered to be the cause of these changes. Manipulating microbial populations with probiotics in the presence of proper diets can reduce enteritis, improve intestinal barrier integrity, and increase the number of beneficial bacteria, which leads to weight loss. Improvement of intestinal dysbiosis and obesity in animals and humans have been reported as a result of the use of probiotics. However, animal studies still prevail, while there is little research on the effects of probiotics on SCFAs content in human feces. The administration of the probiotic strain Lactobacillus acidophilus DDS-1 has been shown to modulate the intestinal microbiome and the associated metabolic phenotype in aging mice. Probiotic administration increased the number of beneficial bacteria such as Akkermansia spp. and Lactobacillus spp and also caused an increase in butyric acid concentration, while reducing the production of inflammatory cytokines in serum and colonic explants. The results of many other animal studies indicate that supplementation with probiotic Lactobacillus spp. bacteria induced SCFAs production by modulation of the intestinal microbiome. For example, the probiotic bacteria Bifidobacterium pseudocatenulatum CECT 7765 administered to rats that received high-fat diets had an effect on increasing the intestinal barrier function, reducing endotoxemia and accelerating metabolism. Satisfactory results for Lactobacillus plantarum strain no. 14 on improving metabolism have been shown in studies on obesity in animal models. Other studies tested the efficacy of probiotic VSL#3 in preventing and treating obesity and diabetes in several mouse models. It was confirmed that probiotic formula VSL#3 suppressed body weight gain and insulin resistance via modulation of the gut flora composition. In addition, it was found that VSL#3 promoted the release of the hormone GLP-1, resulting in reduced food intake and improved glucose tolerance. The VSL#3-induced changes were associated with an increase in the levels of a short-chain fatty acid (SCFAs), butyrate. In another study feces from 40 Malaysian school-age children (19 of normal weight and 21 overweight children) who consumed a probiotic drink containing the Lactobacillus casei Shirota strain in two stages (four weeks each) were examined. It was found that the consumption of the probiotic drink caused a significant increase in the number of Lactobacillus spp. and Bifidobacterium spp. in the composition of intestinal microbiota of overweight children. Both in normal weight and overweight children after four weeks of supplementation, a significant increase in SCFAs concentration, especially of propionic acid, was observed. In addition, a higher SCFAs concentration (especially butyric and propionic acid) was observed in the stool of overweight children than in normal weight children (Table 5). Also, when Lactobacillus casei Shirota was administered to children with obesity for six months, there was an improvement in the profile of intestinal microbiota and an increase in the concentration of acetic acid in the faces of children with obesity (Table 5).

32Diabetes may be closely associated with a higher risk of CVD. This is due to the compensatory effect leading to hyperinsulinemia and ultimately to various metabolic abnormalities. People with diabetes are also characterized by an altered intestinal microbiome, which can cause obesity, metabolic endotoxemia, B-cell dysfunction, systemic inflammation, and oxidative stress related to disease. As a result of intestinal microbiome imbalance in T2D, production of SCFAs is reduced. Probiotic therapy due to the increased production of SCFAs by intestinal bacteria as well as other functions may be effective in the treatment of diabetes.

33In the study on 60 mice for 6 weeks, the anti-diabetic mechanisms of probiotics composed of 14 strains (Lactobacillus plantarum, Lactobacillus helveticus, Lactococcus lactis, Lactobacillus pentosus, Lactobacillus paracasei, Lactobacillus paracasei sbusp.tolerans, Lactobacillus mucosae, Lactobacillus rhamnosus, Lactobacillus harbinensis and Lactobacillus hilgardii, Issatchenkia orientalis, Candida ethanolica, Kluyveromyces marxianus, Pichia membranifaciens) isolated from traditional fermented camel milk was tested. It was found that tested probiotics improve blood glucose and blood lipid parameters, which can lead to delayed development of T2D. In addition, these probiotics improve the function of the intestinal microbiome by increasing the levels of SCFA-producing bacteria (including lactic acid bacteria, Bifidobacterium, Clostridium leptum, Roseburia) and SCFAs (propionic acid and butyric acid) as well as the expression of cluaudin-1 and mucin -2, and decreasing Escherichia coli and lipopolysaccharide levels. The results obtained in these studies indicated that 14 composite probiotics might be considered to be a potential treatment method for treating patients with T2D.

34The aim of other studies was to determine the effect of probiotic (fermented goat’s milk containing Lactobacillus acidophilus La-5 and Bifidobacterium animalis subsp. lactis BB-12) on glycemic control, lipid profile, inflammation, oxidative stress and SCFAs in T2D. In a double-blind, randomized, placebo-controlled trial 50 volunteers consumed daily 120 g/d of fermented milk for 6 weeks. The control sample was the group receiving conventional fermented goat milk contained Streptococcus thermophilus TA-40. At end of trial, the proportion of propionic: acetic: butyric acids, taking into account the mean values, was also similar: 10:8:1 in the control group and 14:10:1 in the probiotic group. The authors found that administration of the test probiotic improves glycemic control in people with T2D, however, the intake of fermented goat’s milk seems to be involved with changes in inflammatory cytokines (TNF-α and resistin) and in the acetic acid concentrations (Table 5).

35CVD is the main cause of morbidity and mortality in the world, there is currently a search for methods of treating elevated blood cholesterol. Researchers suggest that high-fat diet consumption has been associated with gut dysbiosis and lead to dyslipidemia, hypertension and T2D mellitus. In addition, SCFAs have the ability to modulate CVD risk factors, including blood pressure reduction and regulation of glucose and lipid homeostasis.

36To this end, the impact of Daily Body Restore (DBR) (a proprietary blend of nine probiotic organisms of the genera Lactobacillus and Bifidobacterium and ten digestive enzymes) on cholesterol metabolism using an in vitro system and a mouse model of hypercholesterolemia induced by a high fat diet. Hypercholesterolemic mice were supplemented with DBR in their drinking water for eight weeks and compared to control mice given low fat diets or unsupplemented high fat diets. As a result, it was found that the probiotic-enzyme supplement used increased the microbiological production of propionic acid in colon reactors and also lowered harmful LDL and increased HDL levels in a mouse model.

37A different study was designed to determination of the probiotic effect of Lactobacillus fermentum 296 on cardiometabolic disorders induced by high-fat diet in a rat model. The probiotic was administrated by oral gavage to rats for 4 weeks. Results of this research suggest the ability of Lactobacillus fermentum 296 improve cardiovascular and biochemical parameters altered in cardiometabolic disorders. The increased production of short-chain fatty acids which modulate vasodilatation and induce hypotension has been proposed as possible mechanism of action this probiotic strain.

38ASD is a collection of neurodevelopmental disorders (including impaired social interaction, communication, and repetitive and stereotyped patterns of behaviors) with evidence of genetic predisposition. Intestinal imbalance and compositional changes in gut microbiome in ASD patients are reported. However, the role of intestinal microbiome in brain disorders is poorly documented. Children with ASD have often been reported to have gastrointestinal problems that are more frequent and more severe than in children from the general population. A strong correlation of gastrointestinal symptoms with the severity of ASD was confirmed in studies of the feces 58 children with ASD (of which half received a daily probiotic and half did not receive one) and 39 healthy children (who did not receive a probiotic). In the feces of children with ASD, significantly lower levels of SCFAs (including acetate, propionate and valerate) compared to healthy children and children with ASD taking probiotics were found. In addition, results of these research indicate an imbalance of gut microbiota in children with ASD (Table 5).

39Presumably, intestinal microbiome dysbiosis is also associated with AD. This was confirmed in studies in which 19 children with atopic dermatitis and 18 healthy individuals were given a probiotic (Bifidobacterium breve BR03, Lactobacillus salivarius LS01) for 20 days. It was found that AD is characterized by dysbiosis of the intestinal microbiome with a predominance of some species such as Faecalibacterium, Oscillospira, Bacteroides, Parabacteroides, and Sutterella, that can act as possible biomarkers associated with the disease. In addition, a reduction or absence of some microorganisms, including those producing SCFAs (Bifidobacterium, Blautia, Coprococcus, Eubacterium, and Propionibacterium) with anti-inflammatory effects or involved in immune homeostasis, which might have a protective role against AD, has been identified. However, no significant changes were observed in the composition of intestinal microorganisms and the concentration of SCFAs in children with AD as a result of probiotic supplementation (Table 5). Therefore, differences in the composition of the intestinal microbiome of healthy children and those with AD may suggest that other probiotics be tested to restore intestinal homeostasis.

40SCFAs have a significant impact on preventing colonization of intestinal epithelium by pathogens. Current research shows that the effect of probiotic microorganisms in preventing pathogen infection is maintaining intestinal barrier or immune regulation. Research on probiotics in gastrointestinal disorders has made huge progress in recent years. According to scientists Lactobacillus casei has anti-inflammatory effects on human intestinal epithelial cells infected by Shigella. In addition, probiotic formulas can treat and prevent diarrhea caused by bacterial and viral infections. Probiotics are effective in preventing Clostridium difficile infection. Twenty-two children with shigellosis and 11 children with salmonellosis were examined for ten days, Lactobacillus rhamnosus GG and comparatively antibacterial drug (TMP-SMX or Polymyxin) were administered for five days and then the SCFAs content in the feces was evaluated. Iso-caproic acid was not found in children receiving the probiotic strain, but an increase in fecal propionic acid concentration was observed. Iso-caproic acid is not found in healthy adults and may be indicative of Clostridium difficile (Table 5). Probiotics prevented C. difficile infection and in randomized clinical studies, prophylactic supplementation of Lactobacillus GG (LGG) to children reduced the incidence of HRV disease.

41Maintaining the balance of the intestinal microbiome is crucial for maintaining normal human health and preventing many diseases. Short-chain fatty acids, as metabolites of intestinal bacteria, perform many important functions. The concentration of SCFAs depends on the composition and size of the population of intestinal microorganisms, genetic factors, environmental factors and the diet conditioning access to appropriate substrates. Imbalance of the intestinal microbiome and a decrease in the number of bacteria producing metabolites such as SCFAs (e.g., acetic, propionic and butyric acid) are often diagnosed in patients with inflammatory bowel diseases (IBD), irritable bowel syndrome (IBS), type 2 diabetes (T2D), obesity, infections bacterial, autoimmune disorders, or cancer patients. Numerous scientific reports confirm the effectiveness of probiotics in modulating the intestinal microbiome and their effect on the SCFAs content in the colon. Many studies, in addition to acting in the digestive system, concern the effect of SCFAs produced by intestinal microbiome on functions of distant tissues and organs. Researchers highlight the immunomodulatory effect of SCFAs produced by probiotics, but the mechanisms of their action still need further study. The use of probiotic microorganisms to prevent and treat intestinal dysbiosis, leading to an increase in SCFAs in the colon, seems to be an important direction for further research. Research on SCFAs in relation to diseases covered by the review is much-needed to understand their etiology and pathogenesis, and to propose new therapies. Clinical studies in human populations in this area are highly desirable.