Abstract
p-cresol is a metabolite produced by microbial metabolism of aromatic amino acid tyrosine. p-cresol and its conjugated forms, p-cresyl sulfate and p-cresyl glucuronide, are uremic toxins that correlate positively with chronic kidney disease and diabetes pathogenesis. However, how p-cresol affects gut hormones is unclear. Here, we expose immortalized GLUTag cells to increasing concentrations of p-cresol and found that p-cresol inhibited Gcg expression and reduced glucagon-like peptide-1 (GLP-1) secretion in vitro. In mice, administration of p-cresol in the drinking water for 2 weeks reduced the transcript levels of Gcg and other gut hormones in the colon; however, it did not affect either fasting or glucose-induced plasma GLP-1 levels. Furthermore, it did not affect glucose tolerance but promoted faster small intestinal transit in mice. Overall, our data suggest that microbial metabolite p-cresol suppresses transcript levels of gut hormones and regulates small intestinal transit in mice.
| Originalsprog | Engelsk |
|---|---|
| Artikelnummer | 1200391 |
| Tidsskrift | Frontiers in Endocrinology |
| Vol/bind | 14 |
| Antal sider | 7 |
| ISSN | 1664-2392 |
| DOI | |
| Status | Udgivet - 2023 |
Bibliografisk note
Funding Information:The study is funded by the Novo Nordisk Foundation (NNF15OC0016798) and the Transatlantic Network of Excellence Award from the Leducq Foundation (17CVD01). FB is Torsten Söderberg Professor in Medicine and Wallenberg Scholar. Acknowledgments
Publisher Copyright:
Copyright © 2023 Toft, Vanslette, Trošt, Moritz, Gillum, Bäckhed and Arora.
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