Tian Tang
Jing Wang†- Chongqing Tianyou Dairy Co., Ltd., Chongqing, China
Probiotics have received widespread attention as a healthy ingredient. The preventive effect of Bifidobacterium lactis TY-S01 on loperamide-induced constipation in mice was investigated in this study. TY-S01 accelerated the peristalsis of intestine, maintained the humidity of faeces, and prevented the destruction of gut barrier. TY-S01 also maintained the 5-HT, MTL and SP at normal levels in constipated mice. Simultaneously, TY-S01 up-regulated the mRNA expressions of 5-HT4R, SERT, and MUC-2, while down-regulated the mRNA expressions of pro-inflammatory genes remarkably. The levels of short-chain fatty acids in the feces of constipated mice were also increased because of the intervention with TY-S01. Moreover, TY-S01 prevented gut microbiological dysbiosis in constipated mice. Spearman’s correlation analysis revealed that there was an obvious association between metabolic biomarkers and gut microbiota. In summary, TY-S01 regulated gut microbiota and the production of intestinal metabolites to prevent loperamide-induced constipation.
Introduction
Constipation is a prevalent gastrointestinal disease characterized by reduced stool volume, dry stools, difficulty defecation, and infrequent bowel movements (1). Drugs are frequently utilized to treat constipation currently, however, the therapy gives rise to many complications such as severe diarrhea and drug dependence (2). Hence, efficacious treatments without side effects are being expected.
The latest research has revealed that dysbiosis of gut microbiota increases constipation. Decreased abundance of beneficial bacteria while the excessive abundance of opportunistic pathogens in the gut of constipated individuals has been reported (3). The inflammatory response, impaired intestinal mucosal barrier, reduced intestinal metabolites, intestinal dysfunction, abnormal neurotransmitter, and neurochemical signaling caused by the dysbiosis of gut microbiota can decelerate intestinal motility, thereby contributing to constipation (4–6). Intestinal metabolites short-chain fatty acids (SCFAs) are beneficial, which promote intestinal motility by reducing intestinal pH and inhibiting inflammation (7). The 5-hydroxytryptamine (5-HT) is mainly synthesized in the gut and is a pivotal neurotransmitter of the brain–gut axis (8). 5-HT receptor 4 (5-HT4R) is a specific receptor for 5-HT, which contributes to ameliorating constipation (9). Serotonin transporter (SERT) is a transmembrane transporter responsible for transporting 5-HT (2). Therefore, the down-regulated expression of SERT and 5-HT4R predicts intestinal dysfunction.
Probiotics, including Bifidobacterium and Lactobacillus, have been confirmed to have multiple health benefits. Recent studies suggested that probiotics could influence the development of constipation by affecting the intestinal transit time, the stool frequency and consistency, and the gut microbiota (10). Agrawal et al. put forward that Bifidobacterium lactis DN173010 shortened the time of intestinal transit by an average of 12.2 h (11). The research by Yang et al. determined that dietary synbiotics (Bifidobacterium animalis subsp. lactis, Lactobacillus rhamnosus, Lactobacillus acidophilus, and Lactobacillus plantarum participated in the composition) alleviated constipation via increasing the population of beneficial bacteria, stimulating the emancipation of gastrointestinal hormones and repressing the inflammatory response in mice (12). Not exclusively, another report verified that Bifidobacterium heightened the population of Lactobacillus but lowered the population of Odoribacter and Clostridium in the gut to attenuate constipation in mice, and illustrated interspecies differences (13). Wang et al. proposed that B. animalis subsp. lactis MN-Gup relieved constipation by enhancing the levels of intestinal SCFAs (14). Furthermore, the emancipation of 5-HT was promoted and the expressions of SERT and 5-HT4R were up-regulated after the supplementation of Lactobacillus paracasei X11 and prebiotics in constipated mice (2). Probiotics are “strain-specific” in their efficacy. Therefore, the selection and breeding of probiotics with excellent performance in preventing constipation will contribute to enriching probiotic resources and provide more personalized choices.
In this study, we provided a probiotic strain, B. lactis TY-S01, and surveyed its preventive effect on loperamide-induced constipation of mice. Furthermore, the potential mechanism of TY-S01 to prevent constipation was explored.
Materials and Methods
Materials
Bifidobacterium lactis TY-S01 was separated from the intestine of long-lived elderly in Bama, Guangxi, China, and was preserved in the China General Microbiological Culture Collection Center (Beijing, China) with the accession No. 21255. The colony number was adjusted to 1.0 × 109 CFU/kg.BW before gavage.
Animal Experiments
The animal experimental scheme was authorized by the Experimental Animal Welfare Ethics Review Committee of Chongqing Institute of Traditional Chinese Medicine (5001087226041, Chongqing, China). Seven-week-old BALB/c male mice were housed in a standardized laboratory and fed under standard conditions. The experiment was started after 1 week of adaptive feeding. Mice were divided into three groups randomly, namely control (NC), constipation model (CM), and TY-S01 intervention (TY-S01) group containing 10 mice each. The experiment was divided into two periods, the TY-S01 intervention period and constipation modeling period, respectively, and the model design and the dosage of loperamide referred to the method of Wang et al. (15). In the TY-S01 intervention period (1–14 days): the NC group and CM group were given normal saline while the TY-S01 group was given 109 CFU/kg.BW bacterial solution. In the constipation modeling period (15–17 days): all of the groups were gavaged 10 mg/kg.BW loperamide except for the NC group, the mice of the NC group were given normal saline. The mice were administered again as similar to the TY-S01 intervention period after an interval of 1 h. The gavage volume was 10 mL/kg.BW throughout the whole experiment. On the 17th day, all mice were fasted for 16 h after the gavage and then given 10 ml/kg.BW of activated carbon solution (18th day). Five mice in each group were used to measure the time of the first black stool (FBS), and the remaining five mice were used to measure the gastrointestinal transit rate (GTR). All mice had free access to water and food during the experiment, and the weight of the mice was recorded.
Sample Collection
The feces of mice in each group on day 17 were collected for the determination of fecal water content (FWC) and fecal SCFAs level. After the experiment, blood was collected, and the serum was obtained after refrigerated centrifugation at 3,000 g for 15 min for biochemical analysis and metabolomics analysis; small intestine and colon tissues were collected for histological observation and real-time PCR; the cecal contents of each mouse were collected for microbiome analysis.
Measurement of Time of First Black Stool
Mice were placed in a clean cage individually and the time that each mouse excreted its FBS was recorded.
Measurement of Fecal Water Content
The wet weight of the feces was measured after the defecation of the mice instantly, then the feces were thoroughly dried in an oven and weighed again to obtain the dry weight. FWC was calculated in the light of following formula: FWC(%)=[(wetweight−dryweight)/wetweight]×100%.
Measurement of the Gastrointestinal Transit Rate
The mice were sacrificed 20 min after gavage with activated carbon and the whole intestines were collected to survey the transit distance of activated charcoal. GTR was calculated in the light of following formula: GTR(%)=(charcoalmarker/intestinallength)×100%.
Histological Analysis of the Small Intestine
About 0.5 cm of intestinal segments were cut, washed with saline, and fixed in 4% paraformaldehyde, embedded and paraffin sectioned within 72 h, then the fixed intestinal segments were routinely stained with hematoxylin and eosin (H&E) (2). An inverted fluorescence microscope (Leica DMi8, Weztlar, Germany) was used to observe the tissue state.
Measurement of the Biochemical Indicators
The levels of 5-HT, motilin (MTL), and substance P (SP) were surveyed in the serum of mice using an enzyme-linked immunosorbent assay kit (Elisa Biotech Co., Ltd., Shanghai, China).
Measurement of mRNA Expression by RT-PCR
Total RNA from colon tissues was extracted with TRIzol (Invitrogen, CA, United States). cDNA was synthesized by reverse transcription of 1 μg RNA using the RevertAid First Strand cDNA Synthesis Kit (Invitrogen, CA, United States). The level of mRNA expressions was measured by a real-time PCR machine (Bio-Rad, CA, United States). Primer sequences are shown in Table 1 (GAPDH as reference gene). The relative expression of mRNA was computed using the 2–ΔΔCT method.
Table 1. The sequences of the target gene.
Measurement of the Short-Chain Fatty Acids by GC
About 50 mg of feces were added to saturated sodium chloride solution, followed by acidification with 10% sulfuric acid and extraction with 1,000 μl of ether. The supernatant was added with 0.25 g of anhydrous sodium sulfate, and the supernatant was collected again (16). Chromatography was performed using a GC-7890A (Agilent Technologies Inc., CA, United States) with a flame ionization detector. GC conditions: the initial temperature was 100°C, maintained for 5 min, increased to 250°C at a rate of 10°C min–1, and held for 12 min. The injection volume was 1 μl.
Analysis of the Microbial Diversity
Eight samples of cecal contents were randomly selected from each group for gut microbiota analysis. The ABI GeneAmp® 9700 PCR thermocycler (ABI, CA, United States) was used to amplify the hypervariable region V3–V4 of the bacterial 16S rRNA gene with primer pairs 338F (5′-ACTCCTACGGGAGGCAGCAG-3′) and 806R (5′-GGACTACHVGGGTWTCTAAT-3′). Sequencing was performed using an Illumina NovaSeq PE250 platform (Illumina, San Diego, CA, United States) according to the standard protocols by Majorbio Bio-Pharm Technology Co., Ltd. (Shanghai, China). The data were analyzed on the online platform of Majorbio Cloud Platform.1 The representative sequences for the ASVs were annotated using the Bayes annotation method and through the Silva 138/16S-bacteria database. In order to complete the subsequent analysis, sequences were rarefied to the lowest number of sequences per sample (n = 25,359 sequences).
Statistical Analysis
The difference between groups was compared by one-way ANOVA and Tukey’s test using SPSS version 20.0 software. Figures were made using GraphPad Prism 7.0 software. A p < 0.05 was considered statistically significant.
Results
TY-S01 Prevented Loperamide-Induced Constipation in Mice
The mice was treated with TY-S01 for 14 days followed by giving with loperamide for 3 days to assess the effect of TY-S01 on constipation. Body weight had no obvious difference in mice during the experiment (p < 0.05) (Figure 1A), illustrating that the mice were in good physiological status. The consequence demonstrated that TY-S01 intervention shortened the time of FBS remarkably and maintained the FWC in constipated mice (p < 0.05, Figures 1B,C). Besides, the GTR in the CM group was dramatically lower than in the NC group, while increased in the TY-S01 group (p < 0.05, Figures 1D,E). Hence, TY-S01 treatment prevented constipation in mice effectively.
Figure 1. TY-S01 prevented loperamide-induced constipation in mice. (A) Body weight; (B) the time of the first black stool; (C) fecal water content; (D) intestinal advancement distance; (E) gastrointestinal transit rate; and (F) small intestinal sections stained with hematoxylin and eosin. NC is the normal control group; CM is the constipation model group; TY-S01 is the treatment group with TY-S01. # represents the significant difference between the NC and CM groups (p < 0.05); * represents the significant difference between the CM and TY-S01 groups (p < 0.05). Data are presented as mean ± SD.
The effect of TY-S01 on intestinal morphology was determined in constipated mice by histological staining. H&E staining revealed that loperamide caused the fractured and uncomplete villi in the small intestine, while TY-S01 maintained the integrity of the ileal wall and villi. Furthermore, TY-S01 administration suppressed the lamina propria cell infiltration in the intestine (p < 0.05, Figure 1F). The results illustrated that TY-S01 maintained intestinal epithelial integrity in constipated mice.
Effect of TY-S01 on the Levels of 5-Hydroxytryptamine and Gastrointestinal Hormone in Serum of Mice
The effect of TY-S01 on the serum level of 5-HT, MTL, and SP is displayed in Figure 2. The 5-HT, MTL, and SP levels in the CM group were notably reduced compared to the NC group (p < 0.05). However, 5-HT, MTL, and SP remained at normal levels after TY-S01 treatment (p < 0.05). The results suggested that the mechanism by which TY-S01 prevented constipation was associated with the release of 5-HT and gastrointestinal hormones probably.
Figure 2. Effect of TY-S01 on the levels of 5-HT and gastrointestinal hormone in serum of mice. The serum level of 5-HT (A), MTL (B), and SP (C). 5-HT is 5-hydroxytryptamine; MTL is motilin; SP is substance P. NC is the normal control group; CM is the constipation model group; TY-S01 is the treatment group with TY-S01. # represents the significant difference between the NC and CM groups (p < 0.05); * represents the significant difference between the CM and TY-S01 groups (p < 0.05). Data are presented as mean ± SD.
Effect of TY-S01 on Intestinal Function and Intestinal Inflammation of Mice
The effect of TY-S01 on function, mucosal barrier, and inflammation in the colon of mice was assessed by RT-PCR. In the CM group, the mRNA expression of 5-HT4GPCR and SERT was lessened obviously (p < 0.05, Figures 3A,B). TY-S01 treatment maintained the mRNA expressions of 5-HT4G and SERT at normal levels (p < 0.05, Figures 3A,B), which attenuated intestinal dysfunction in constipated mice. The MUC-2 was the element of intestinal tight junction, and the MUC-2 mRNA expression was down-regulated in the CM group but was up-regulated significantly in the TY-S01 group (p < 0.05, Figure 3C). Moreover, the mRNA expression levels of TNF-α, IL-6, and IL-1β were decreased in mice of the CM group compared with the NC group, TY-S01 suppressed the expression of TNF-α, IL-6, and IL-1β meaningfully (p < 0.05, Figures 3D–F). The consequences proved that TY-S01 attenuated intestinal inflammation in constipated mice.
Figure 3. Effect of TY-S01 on intestinal function and intestinal inflammation of mice. The mRNA expression levels of 5-HT4R (A), SERT (B), MUC-2 (C), TNF-α (D), IL-6 (E), and IL-1β (F). 5-HT4R is 5-HT receptor 4; SERT is serotonin transporter; MUC-2 is mucin 2; TNF-α is tumor necrosis factor-α; IL-6 is interleukin-6; IL-1β is interleukin-1β. NC is the normal control group; CM is the constipation model group; TY-S01 is the treatment group with TY-S01. # represents the significant difference between the NC and CM groups (p < 0.05); * represents the significant difference between the CM and TY-S01 groups (p < 0.05). Data are presented as mean ± SD.
Effect of TY-S01 on the Structure of Gut Microbiota in Mice
The effect of TY-S01 on gut microbiota in constipated mice was explored by 16S rDNA sequencing technology. Chao index and Shannon index are α-diversity indices, which are utilized to assess the richness and diversity of a community, respectively. Chao index and Shannon index were reduced in the CM group, but higher in the NC group and TY-S01 group (p < 0.05, Figures 4A,B). The β-diversity between microbiome samples was determined via the non-metric dimensional scaling (NMDS), which illustrated that the cluster of the TY-S01 group was similar to the NC group but relatively separated from the CM group (Figure 4C). Therefore, even after loperamide treatment, TY-S01 maintained the gut microbiota of mice in a balanced state.
Figure 4. Effect of TY-S01 on the structure of gut microbiota in mice. (A) Chao index; (B) Shannon index; and (C) NMDS at the ASV level. NMDS is non-metric multidimensional scaling; ASV is amplicon sequence variants. NC is the normal control group; CM is the constipation model group; TY-S01 is the treatment group with TY-S01. # represents the significant difference between the NC and CM groups (p < 0.05); * represents the significant difference between the CM and TY-S01 groups (p < 0.05). Data are presented as mean ± SD.
Effect of TY-S01 on the Composition of Gut Microbiota in Mice
The effect of TY-S01 on the abundance of special species in the gut of mice was explored at the phylum, family, and genus levels, respectively. At the phylum level, the ratio of Firmicutes to Bacteroidetes was increased because of TY-S01 in constipated mice (p < 0.05, Figures 5A,C). Meanwhile, the abundance of Proteobacteria in the CM group was significantly higher than that in the TY-S01 group and NC group (p < 0.05, Figures 5A,D). At the family level, loperamide decreased the populations of Lachnospiraceae, Bacteroidaceae, and increased the population of Ruminococcaceae (p < 0.05, Figures 5B,E–G). However, TY-S01 maintained the normal abundance of these species (p < 0.05, Figures 5B,E–G). At the genus level, compared with the TY-S01 group, the abundance of Escherichia–Shigella, Parasutterella, Clostridium-sensu-stricto-1, and Clostridioides in the CM group was significantly increased while the abundance of unclassified-f-Lachnospiraceae, Desulfovibrio, Eubacterium-brachy-group and Lachnospiraceae-UCG-006 was significantly reduced (Figures 5H,I).
Figure 5. Effect of TY-S01 on the composition of gut microbiota in mice. (A) Taxonomic distribution of bacterial communities at the phylum level; (B) taxonomic distribution of bacterial communities at the family level; (C) the ratio of Firmicutes to Bacteroidetes; (D) the relative abundance of Proteobacteria; (E) the relative abundance of Lachnospiraceae; (F) the relative abundance of Bacteroidaceae; (G) the relative abundance of Ruminococcaceae; (H) taxonomic distribution of bacterial communities at the genus level; and (I) species difference analysis at the genus level. NC is the normal control group; CM is the constipation model group; TY-S01 is the treatment group with TY-S01. # represents the significant difference between the NC and CM groups (p < 0.05); * represents the significant difference between the CM and TY-S01 groups (p < 0.05). Data are presented as mean ± SD. *, **, and *** represent 0.01 < p ≤ 0.05, 0.001 < p ≤ 0.01, and p ≤ 0.001, respectively.
Effect of TY-S01 on the Short-Chain Fatty Acids Content in Feces of Mice
GC was utilized to determine the effect of TY-S01 on the content of SCFAs in feces. The acetic acid (AA), butyric acid (BA), and valeric acid (VA) were obviously decreased in the CM group compared to the NC group (p < 0.05, Figures 6A,C,E). Although the levels of propionic acid (PA) and isobutyric acid (IBA) also declined, there was no statistical difference (p < 0.05, Figures 6B,D). The levels of AA, PA, BA, IBA, and VA in the TY-S01 group were significantly higher compared to the CM group (p < 0.05, Figures 6A–E). Apparently, TY-S01 maintained the levels of SCFAs, which provided assistance to prevent constipation possibly.
Figure 6. Effect of TY-S01 on the SCFAs content in feces of mice. The fecal levels of acetic acid (A), propionic acid (B), butyrate acid (C), isobutyrate acid (D), and valeric acid (E). NC is the normal control group; CM is the constipation model group; TY-S01 is the treatment group with TY-S01. # represents the significant difference between the NC and CM groups (p < 0.05); * represents the significant difference between the CM and TY-S01 groups (p < 0.05). Data are presented as mean ± SD.
Correlations Analysis Between Gut Microbiota and Metabolic Biomarkers
Spearman’s correlation analysis was used to clarify the association of metabolic biomarkers of constipation with the top 50 species at the genus level (Figure 7). Lachnospiraceae-NK4A136-group, Desulfovibrio, Eubacterium-brachy-group, and lachnospiraceae-UCG-006 were positively associated with metabolic biomarkers (5-HT, MTL, SP, AA, PA, BA, IBA, and VA). The unclassified-f-Lachnospiraceae was positively correlated with all of the above metabolic biomarkers but not IBA. The SP and AA were negative correlations with Escherichia-Shigella and Clostridium-sensu-stricto-1 was negatively related to SP, AA, PA, BA, and VA. Moreover, the 5-HT, AA, PA, and BA were a negative association with Parasutterella. The above data indicated that the evolvement of constipation was closely associated with the gut microbiota.
Figure 7. Correlation analysis between gut microbiota and metabolic biomarkers at the genus level. The color ranges from blue to red, indicating the change in correlation from negative to positive. HT is 5-hydroxytryptamine; MTL is motilin; SP is substance P; AA is acetic acid; PA is propionic acid; BA is butyrate acid; IBA is isobutyrate acid; VA is valeric acid. Asterisks *, **, and *** represent 0.01 < p ≤ 0.05, 0.001 < p ≤ 0.01, and p ≤ 0.001, respectively.
Discussion
Recently, probiotics have acquired plenty of attention owing to their efficacy and no side effects (17). In this investigation, we approved that B. lactis TY-S01 modulated gut microbiota and its metabolites to prevent loperamide-induced constipation in mice.
The FWC, time of FBS, and GTR are prerequisite indicators for judging the severity of constipation (18). The supply of loperamide incited reduced FWC, prolonged time to FBS, and decreased GTR in the current study. Our results confirmed the ability of TY-S01 to maintain stool humidity and accelerate intestinal peristalsis.
The damaged intestinal morphology could weaken the frequency and degree of the intestinal peristalsis (19). According to H&E staining, mice in the CM group displayed impaired epithelial integrity of the intestine, the disruption of intestinal villi, and the infiltration of inflammatory cells. Nevertheless, TY-S01 maintained the intestinal morphology to the criterion of the NC group. MUC-2 is mucin that covers intestinal epithelial cells to form a protective layer, which helps maintain the integrity of the intestinal mucosal barrier (20). The MUC-2 expression was increased obviously after the supplementation of TY-S01. Constipation is also correlated to impairment of the intestinal mucosal immune system, and animal models verified a causal relationship between the presence of mucosal inflammation and altered sensorimotor function (21). TY-S01 inhibited mRNA expression of pro-inflammatory mediators, including TNF-α, IL-6, and IL-1β. The reduced inflammatory response in the intestine would help avoid the destruction of tight junction proteins and the subsequent increase in intestinal permeability (22). The results indicated that TY-S01 maintained the integrity of gut barrier and attenuated intestinal inflammation.
5-Hydroxytryptamine is mainly distributed in the digestive tract and is secreted by enterochromaffin cells on intestinal mucosa (23). The release of 5-HT from enterochromaffin cells is one of the main triggers of motor and sensory reflex activity in the gut, so the concentration of 5-HT in serum can be used to determine the changes in intestinal function. As 5-HT enhances diarrhea while lessens in constipation symptoms. The elevation of 5-HT induce the release of gastrointestinal hormones such as SP and MTL (24). The SP and MTL are excitatory neuropeptides and associated with the acceleration of intestinal motility (25, 26). In our study, TY-S01 maintained the 5-HT, SP, and MTL at normal levels in constipated mice. Studies have confirmed that 5-HT needs to bind to specific receptors to function in vivo. 5-HT4R is one of the specific receptors for 5-HT, which is associated with enhanced intestinal propulsion and shortened intestinal transit time (27). Down-regulation of 5-HT4R expression was proposed in constipation patients (28). SERT is a transmembrane transporter and expresses on enterochromaffin membranes and presynaptic membranes devote to the transport of 5-HT secreted in the intestine (2). Lactobacillus could relieve constipation by up-regulating the SERT expression in intestinal epithelial cells (29). Aberrant expressions of 5-HT4R and SERT indicate gastrointestinal dysfunction (2). TY-S01 up-regulated the mRNA expressions of 5-HT4R and SERT remarkably, indicating that TY-S01 contributed to the normalization of intestinal function.
Short-chain fatty acids are the final metabolites of indigestible carbohydrates that are fermented by gut microbiota (including acetic, propionic, isobutyrate, butyrate, valeric, etc.), which promote the normalization of intestinal motility (30, 31). Several studies have indicated that probiotics ensure the levels of SCFAs in the gut, which maintains normal bowel movements (32). Different SCFAs have different divisions of labor in relieving constipation. As the foremost outcome of colonic fermentation, acetic accelerate the absorption of water and electrolytes to stimulate the peristalsis of the intestine (33). Butyrate may affect gut motility by regulating immune system-associated T-reg cells and limiting intestinal inflammatory response (34). Propionic, butyric, and valeric can ameliorate constipation by inducing colonic contractions and acting directly on smooth muscle (35). Our study confirmed that TY-S01 could make the level of SCFAs in constipated mice comparable to normal mice, which will be beneficial to prevent the occurrence of constipation.
Differences in gut microbiota between constipated patients and healthy individuals have been bought forward by numerous studies (36). Similarly, the NMDS displayed that the constipated mice had an unequal microbiota structure compared with normal mice in our study, while the microbiota structure of constipated mice was similar to normal mice after TY-S01 intervention. Chao and Shannon indexes are often used to represent the richness and diversity of the community. TY-S01 was able to maintain the richness and diversity of gut microbiota unaffected when loperamide was administered. We further examined the abundance of specific species in the gut with or without TY-S01 treatment. TY-S01 increased the ratio of Firmicutes to Bacteroidetes, which was consistent with the study by Wang et al. (15). Research indicated that the ratio of Firmicutes to Bacteroidetes was positively related to intestinal propulsion and negatively related to stool consistency (37). The abundance of Proteobacteria was detected to lower significantly in the TY-S01 group. Proteobacteria comprise many pathogenic genera and are believed to be a potential pro-inflammatory phylum (38). The positive association of some species with constipation was inhibited in constipated mice via the TY-S01 intervention, such as Ruminococcaceae, Clostridium-sensu-stricto-1, Parasutterella, and Escherichia-Shigella (12, 39, 40). Furthermore, the populations of Lachnospiraceae, Bacteroidaceae, Desulfovibrio, and Eubacterium-brachy-group were heightened after TY-S01 treatment. Lachnospiraceae facilitates the peristalsis of the intestine and the composite of 5-HT in enterochromaffin cells (41). Bacteroidetes promote the expression of gut-associated proteins to accelerate intestinal motility (42). And Desulfovibrio, Eubacterium-brachy-group have a positive effect on ameliorating constipation (12, 43). Surprisingly, there were obvious associations of metabolic biomarkers with specific species in the intestine by correlation analysis. Our findings suggested that TY-S01 could prevent gut dysbiosis caused by constipation and mediate the production of microbiota metabolites.
Conclusion
Comprehensively, TY-S01 prevented loperamide-induced constipation in mice, involving the acceleration of intestinal peristalsis, the maintenance of feces humidity, the prevention of damaged gut barrier, and the prevention of intestinal dysfunction, and the repression of intestinal inflammatory response. The underlying mechanism was related to maintaining the balance of gut microbiota, accompanied by beneficial modulation of gut metabolites such as SCFAs, 5-HT, and gastrointestinal hormones. The results suggest that TY-S01 should be investigated for its ability to prevent or manage constipation in humans.
Data Availability Statement
The data presented in this study were deposited in the NCBI repository, Submission ID is SUB11203385 and the BioProject ID is PRJNA817683. It can be accessed through the following link: http://www.ncbi.nlm.nih.gov/bioproject/817683.
Ethics Statement
The animal study was reviewed and approved by the Experimental Animal Welfare Ethics Review Committee of Chongqing Institute of Traditional Chinese Medicine (5001087226041, Chongqing, China).
Author Contributions
TT: methodology, investigation, and writing manuscript and editing. JW: methodology, visualization, and formal analysis. YJ and ZZ: resources. XZ, YW, XS, and YD: investigation. FZ: conceptualization, funding acquisition, and supervision. All authors read and approved the final manuscript.
Funding
This study was received funding from Chongqing Science and Technology Bureau, Chongqing, China, and the grant number was cstc2022ycjh-bgzxm0240.
Conflict of Interest
TT, JW, YJ, XZ, ZZ, YW, XS, YD, and FZ were employed by the company Chongqing Tianyou Dairy Co., Ltd.
Publisher’s Note
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Footnotes
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Keywords: probiotics, constipation, gut microbiota, SCFAs, 5-HT, inflammation
Citation: Tang T, Wang J, Jiang Y, Zhu X, Zhang Z, Wang Y, Shu X, Deng Y and Zhang F (2022) Bifidobacterium lactis TY-S01 Prevents Loperamide-Induced Constipation by Modulating Gut Microbiota and Its Metabolites in Mice. Front. Nutr. 9:890314. doi: 10.3389/fnut.2022.890314
Received: 05 March 2022; Accepted: 06 June 2022;
Published: 29 June 2022.
Edited by:
Xin Zhao, Chongqing University of Education, ChinaReviewed by:
Arthur C. Ouwehand, International Flavors & Fragrances, FinlandXin Wang, Zhejiang Academy of Agricultural Sciences, China
Copyright © 2022 Tang, Wang, Jiang, Zhu, Zhang, Wang, Shu, Deng and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Feng Zhang, tyryjszx88@163.com
†These authors have contributed equally to this work and share first authorship