The relationship between bile acid concentration, glucagon-like-peptide 1, fibroblast growth factor 15 and bile acid receptors in rats during progression of glucose intolerance

Abstract Background Recent studies show that bile acids are involved in glucose and energy homeostasis through activation of G protein coupled membrane receptor (TGR5) and farnesoid X receptor (FXR). A few researches have explored changes of TGR5 and FXR in animals with impaired glucose regulation....

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Main Authors: Xinfeng Yan, Peicheng Li, Zhaosheng Tang, Bo Feng
Format: Article
Language:English
Published: BMC 2017-09-01
Series:BMC Endocrine Disorders
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12902-017-0211-5
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spelling doaj-526187d3d19944aaa461bda4068ff79a2020-11-25T03:53:22ZengBMCBMC Endocrine Disorders1472-68232017-09-011711710.1186/s12902-017-0211-5The relationship between bile acid concentration, glucagon-like-peptide 1, fibroblast growth factor 15 and bile acid receptors in rats during progression of glucose intoleranceXinfeng Yan0Peicheng Li1Zhaosheng Tang2Bo Feng3Department of Endocrinology, Shanghai East Hospital, Tongji University School of MedicineDepartment of Endocrinology, Shanghai East Hospital, Tongji University School of MedicineDepartment of Endocrinology, Shanghai East Hospital, Tongji University School of MedicineDepartment of Endocrinology, Shanghai East Hospital, Tongji University School of MedicineAbstract Background Recent studies show that bile acids are involved in glucose and energy homeostasis through activation of G protein coupled membrane receptor (TGR5) and farnesoid X receptor (FXR). A few researches have explored changes of TGR5 and FXR in animals with impaired glucose regulation. This study aimed to observe changes of plasma total bile acids (TBA), glucagon-like-peptide 1 (GLP-1), fibroblast growth factor 15 (FGF15), intestinal expressions of TGR5 and FXR, and correlations between them in rats with glucose intolerance. Methods Besides plasma fasting glucose, lipid, TBAs, alanine transaminase (ALT), active GLP-1(GLP-1A) and FGF15, a postprandial meal test was used to compare responses in glucose, insulin and GLP-1A among groups. The expressions of TGR5 and FXR in distal ileum and ascending colon were quantified by real-time PCR and western blot. Results TGR5 expression was significantly decreased in distal ileum in DM group compared to other groups, and TGR5 and FXR expressions in ascending colon were also decreased in DM group compared to other groups. Correlation analysis showed correlations between TBA and GLP-1A or FGF15. GLP-1A was correlated with TGR5 mRNA expression in colon, and FGF15 was correlated with FXR mRNA expression in colon. Conclusions These results indicates that bile acid-TGR5/FXR axis contributes to glucose homeostasis.http://link.springer.com/article/10.1186/s12902-017-0211-5Impaired glucose toleranceType 2 diabetes mellitusBile acid receptorsGLP-1FGF15
collection DOAJ
language English
format Article
sources DOAJ
author Xinfeng Yan
Peicheng Li
Zhaosheng Tang
Bo Feng
spellingShingle Xinfeng Yan
Peicheng Li
Zhaosheng Tang
Bo Feng
The relationship between bile acid concentration, glucagon-like-peptide 1, fibroblast growth factor 15 and bile acid receptors in rats during progression of glucose intolerance
BMC Endocrine Disorders
Impaired glucose tolerance
Type 2 diabetes mellitus
Bile acid receptors
GLP-1
FGF15
author_facet Xinfeng Yan
Peicheng Li
Zhaosheng Tang
Bo Feng
author_sort Xinfeng Yan
title The relationship between bile acid concentration, glucagon-like-peptide 1, fibroblast growth factor 15 and bile acid receptors in rats during progression of glucose intolerance
title_short The relationship between bile acid concentration, glucagon-like-peptide 1, fibroblast growth factor 15 and bile acid receptors in rats during progression of glucose intolerance
title_full The relationship between bile acid concentration, glucagon-like-peptide 1, fibroblast growth factor 15 and bile acid receptors in rats during progression of glucose intolerance
title_fullStr The relationship between bile acid concentration, glucagon-like-peptide 1, fibroblast growth factor 15 and bile acid receptors in rats during progression of glucose intolerance
title_full_unstemmed The relationship between bile acid concentration, glucagon-like-peptide 1, fibroblast growth factor 15 and bile acid receptors in rats during progression of glucose intolerance
title_sort relationship between bile acid concentration, glucagon-like-peptide 1, fibroblast growth factor 15 and bile acid receptors in rats during progression of glucose intolerance
publisher BMC
series BMC Endocrine Disorders
issn 1472-6823
publishDate 2017-09-01
description Abstract Background Recent studies show that bile acids are involved in glucose and energy homeostasis through activation of G protein coupled membrane receptor (TGR5) and farnesoid X receptor (FXR). A few researches have explored changes of TGR5 and FXR in animals with impaired glucose regulation. This study aimed to observe changes of plasma total bile acids (TBA), glucagon-like-peptide 1 (GLP-1), fibroblast growth factor 15 (FGF15), intestinal expressions of TGR5 and FXR, and correlations between them in rats with glucose intolerance. Methods Besides plasma fasting glucose, lipid, TBAs, alanine transaminase (ALT), active GLP-1(GLP-1A) and FGF15, a postprandial meal test was used to compare responses in glucose, insulin and GLP-1A among groups. The expressions of TGR5 and FXR in distal ileum and ascending colon were quantified by real-time PCR and western blot. Results TGR5 expression was significantly decreased in distal ileum in DM group compared to other groups, and TGR5 and FXR expressions in ascending colon were also decreased in DM group compared to other groups. Correlation analysis showed correlations between TBA and GLP-1A or FGF15. GLP-1A was correlated with TGR5 mRNA expression in colon, and FGF15 was correlated with FXR mRNA expression in colon. Conclusions These results indicates that bile acid-TGR5/FXR axis contributes to glucose homeostasis.
topic Impaired glucose tolerance
Type 2 diabetes mellitus
Bile acid receptors
GLP-1
FGF15
url http://link.springer.com/article/10.1186/s12902-017-0211-5
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