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Improvement of loperamide-induced slow transit constipation by Bifidobacterium bifidum G9-1 is mediated by the correction of butyrate production and neurotransmitter profile due to improvement in dysbiosis.
- Source :
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PloS one [PLoS One] 2021 Mar 22; Vol. 16 (3), pp. e0248584. Date of Electronic Publication: 2021 Mar 22 (Print Publication: 2021). - Publication Year :
- 2021
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Abstract
- A treatment option for constipation that improves the quality of life is needed since available laxatives do not effectively improve the quality of life in patients with constipation. A significant association between gut dysbiosis and constipation is recognized, suggesting that probiotics may be an important option for management of constipation. The underlying mechanism by which probiotics improve constipation remains unclear. In this study, we aimed to evaluate the effects of the probiotic Bifidobacterium bifidum G9-1 (BBG9-1) on loperamide-induced delayed colonic transit constipation and to elucidate its mechanism of action. First, the effect of BBG9-1 was evaluated in a rat model of constipation induced by subcutaneous administration of loperamide. BBG9-1 improved constipation parameters (number of feces, fecal water content, and fecal hardness) in constipated rats. Next, the relationship of organic acids and neurotransmitters to gut microbiota was investigated. BBG9-1 improved dysbiosis and prevented a decrease in butyric acid concentration in the gut, increased serum serotonin, and suppressed an increase in dopamine and a decrease in acetylcholine in serum. Further, an increase in the expression level of tryptophan hydroxylase 1, a 5-HT-synthetizing enzyme, was observed. These results suggest that BBG9-1 improves dysbiosis, which results in an increase in organic acids and improvement of neurotransmission. These actions may increase intestinal mobility, finally leading to alleviating constipation. The probiotic BBG9-1 may, therefore, be a potential option for the treatment of constipation.<br />Competing Interests: The authors have read the journal’s policy and the authors of this manuscript have the following competing interests: YM, TU, HY, MY, YT, HO are paid employees of Biofermin Pharmaceutical Co., Ltd. There are no patents, products in development or marketing products to declare. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
- Subjects :
- Animals
Butyrates metabolism
Butyric Acid metabolism
Constipation etiology
Constipation pathology
Disease Models, Animal
Dopamine biosynthesis
Dopamine genetics
Dysbiosis chemically induced
Dysbiosis complications
Feces microbiology
Gastrointestinal Microbiome drug effects
Gastrointestinal Motility drug effects
Gene Expression Regulation, Enzymologic
Humans
Laxatives pharmacology
Loperamide toxicity
Neurotransmitter Agents metabolism
Probiotics chemistry
Quality of Life
Rats
Serotonin blood
Bifidobacterium bifidum chemistry
Constipation drug therapy
Dysbiosis microbiology
Probiotics pharmacology
Tryptophan Hydroxylase genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 16
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 33750988
- Full Text :
- https://doi.org/10.1371/journal.pone.0248584