Dataset Information


Gut microbes promote colonic serotonin production through an effect of short-chain fatty acids on enterochromaffin cells.

ABSTRACT: Gut microbiota alterations have been described in several diseases with altered gastrointestinal (GI) motility, and awareness is increasing regarding the role of the gut microbiome in modulating GI function. Serotonin [5-hydroxytryptamine (5-HT)] is a key regulator of GI motility and secretion. To determine the relationship among gut microbes, colonic contractility, and host serotonergic gene expression, we evaluated mice that were germ-free (GF) or humanized (HM; ex-GF colonized with human gut microbiota). 5-HT reduced contractile duration in both GF and HM colons. Microbiota from HM and conventionally raised (CR) mice significantly increased colonic mRNAs Tph1 [(tryptophan hydroxylase) 1, rate limiting for mucosal 5-HT synthesis; P < 0.01] and chromogranin A (neuroendocrine secretion; P < 0.01), with no effect on monoamine oxidase A (serotonin catabolism), serotonin receptor 5-HT4, or mouse serotonin transporter. HM and CR mice also had increased colonic Tph1 protein (P < 0.05) and 5-HT concentrations (GF, 17 ± 3 ng/mg; HM, 25 ± 2 ng/mg; and CR, 35 ± 3 ng/mg; P < 0.05). Enterochromaffin (EC) cell numbers (cells producing 5-HT) were unchanged. Short-chain fatty acids (SCFAs) promoted TPH1 transcription in BON cells (human EC cell model). Thus, gut microbiota acting through SCFAs are important determinants of enteric 5-HT production and homeostasis.


PROVIDER: S-EPMC4396604 | BioStudies | 2015-01-01T00:00:00Z

REPOSITORIES: biostudies

Similar Datasets

2016-01-01 | S-EPMC5008845 | BioStudies
2015-01-01 | S-EPMC4393509 | BioStudies
2013-01-01 | S-EPMC3890323 | BioStudies
2018-01-01 | S-EPMC6055526 | BioStudies
2018-01-01 | S-EPMC6003035 | BioStudies
2019-01-01 | S-EPMC6852474 | BioStudies
2019-01-01 | S-EPMC6365670 | BioStudies
2019-01-01 | S-EPMC6619411 | BioStudies
2011-01-01 | S-EPMC3057463 | BioStudies
2019-01-01 | S-EPMC6362283 | BioStudies