High-fat diet promotes gestational diabetes mellitus through modulating gut microbiota and bile acid metabolism

IntroductionGestational diabetes mellitus (GDM) is a condition characterized by glucose intolerance during pregnancy, estimated to affect approximately 20% of the whole pregnancies and is increasing in prevalence globally. However, there is still a big gap in knowledge about the association between...

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Main Authors: Lei Yao, Xuefei Zhou, Xianqi Jiang, Hao Chen, Yuanliang Li, Xiao Xiong, Yan Tang, Haogang Zhang, Pengfei Qiao
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Microbiology
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Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2024.1480446/full
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author Lei Yao
Xuefei Zhou
Xianqi Jiang
Hao Chen
Yuanliang Li
Xiao Xiong
Yan Tang
Haogang Zhang
Pengfei Qiao
author_facet Lei Yao
Xuefei Zhou
Xianqi Jiang
Hao Chen
Yuanliang Li
Xiao Xiong
Yan Tang
Haogang Zhang
Pengfei Qiao
author_sort Lei Yao
collection DOAJ
description IntroductionGestational diabetes mellitus (GDM) is a condition characterized by glucose intolerance during pregnancy, estimated to affect approximately 20% of the whole pregnancies and is increasing in prevalence globally. However, there is still a big gap in knowledge about the association between gut microbiota associated metabolism alterations and GDM development.MethodsAll the participants accomplished the validated internet-based dietary questionnaire for Chinese and serum, fecal samples were collected. HFD, control diet or colesevelam intervention was fed to GDM mice models or Fxr-/- mice models, with or without antibiotics cocktail treatment. Fecal microbiota transplantation were used for further validation. Gut microbiota and metabolites were detected by metagenomic sequencing and high-performance liquid chromatography-mass spectrometry, respectively. Bile acids of serum, fecal samples from human and mice were analysised. Body weight, average feed intake, blood glucose, insulin levels and oral glucose tolerance test was performed among each groups. Expression levels of Fxr, Shp and Fgf15 mRNA and protein were detected by quantitative reverse transcription polymerase chain reaction and western blot, respectively.ResultsOur data indicated that high fat diet (HFD) was linked with higher prevalence of GDM, and HFD was positively associated with poor prognosis in GDM patients. Moreover, compared with normal diet (ND) group, GDM patients from HFD group performed a loss of gut microbiota diversity and enrichment of Alistipes onderdonkii, Lachnospiraceae bacterium 1_7_58FAA, and Clostridium aspaaragiforme while ruduction of Akkermansiaceae, Paraprevotell xylaniphila, and Prevotella copri. Additionally, HFD aggravated GDM in mice and gut microbiota depletion by antibiotics crippled the effect of excess fat intake. BAs profile altered in HFD GDM patients and mice models. Fecal microbiota transplantation (FMT) further confirmed that gut microbiota contributed to bile acids (BAs) metabolic dysfunction during HFD-associated GDM development. Mechanically, HFD-FMT administration activated Fxr, Shp, and Fgf15 activity, disturbed the glucose metabolism and aggravated insulin resistance but not in HFD-FMT Fxr−/− mice and ND-FMT Fxr−/− mice. Furthermore, colesevelam intervention alleviated HFD-associated GDM development, improved BAs metabolism, suppressed Fxr, Shp, and Fgf15 activity only in WT mice but not in the Fxr−/− HFD + Colesevelam group and Fxr−/− HFD group. HFD induced GDM and contributed to poor prognosis in GDM parturients through inducing gut microbial dysbiosis and metabolic alteration, especially appeared in BAs profile. Moreover, Fxr pathway participated in regulating HFD-associated gut microbiota disordered BAs metabolites and aggravating GDM in mice.DiscussionModulating gut microbiota and BAs metabolites could be a potential therapeutic strategy in the prevention and treatment of HFD-associated GDM.
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spelling doaj-art-ef48ac0c066f4fd2800c2a12557d6ffa2025-01-28T06:41:11ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2025-01-011510.3389/fmicb.2024.14804461480446High-fat diet promotes gestational diabetes mellitus through modulating gut microbiota and bile acid metabolismLei Yao0Xuefei Zhou1Xianqi Jiang2Hao Chen3Yuanliang Li4Xiao Xiong5Yan Tang6Haogang Zhang7Pengfei Qiao8Department of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, ChinaDepartment of Gynaecology and Obstetrics, The Center of Red Cross Hospital of Harbin, Harbin, ChinaDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, ChinaDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, ChinaDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, ChinaDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, ChinaDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, ChinaDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, ChinaDepartment of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, ChinaIntroductionGestational diabetes mellitus (GDM) is a condition characterized by glucose intolerance during pregnancy, estimated to affect approximately 20% of the whole pregnancies and is increasing in prevalence globally. However, there is still a big gap in knowledge about the association between gut microbiota associated metabolism alterations and GDM development.MethodsAll the participants accomplished the validated internet-based dietary questionnaire for Chinese and serum, fecal samples were collected. HFD, control diet or colesevelam intervention was fed to GDM mice models or Fxr-/- mice models, with or without antibiotics cocktail treatment. Fecal microbiota transplantation were used for further validation. Gut microbiota and metabolites were detected by metagenomic sequencing and high-performance liquid chromatography-mass spectrometry, respectively. Bile acids of serum, fecal samples from human and mice were analysised. Body weight, average feed intake, blood glucose, insulin levels and oral glucose tolerance test was performed among each groups. Expression levels of Fxr, Shp and Fgf15 mRNA and protein were detected by quantitative reverse transcription polymerase chain reaction and western blot, respectively.ResultsOur data indicated that high fat diet (HFD) was linked with higher prevalence of GDM, and HFD was positively associated with poor prognosis in GDM patients. Moreover, compared with normal diet (ND) group, GDM patients from HFD group performed a loss of gut microbiota diversity and enrichment of Alistipes onderdonkii, Lachnospiraceae bacterium 1_7_58FAA, and Clostridium aspaaragiforme while ruduction of Akkermansiaceae, Paraprevotell xylaniphila, and Prevotella copri. Additionally, HFD aggravated GDM in mice and gut microbiota depletion by antibiotics crippled the effect of excess fat intake. BAs profile altered in HFD GDM patients and mice models. Fecal microbiota transplantation (FMT) further confirmed that gut microbiota contributed to bile acids (BAs) metabolic dysfunction during HFD-associated GDM development. Mechanically, HFD-FMT administration activated Fxr, Shp, and Fgf15 activity, disturbed the glucose metabolism and aggravated insulin resistance but not in HFD-FMT Fxr−/− mice and ND-FMT Fxr−/− mice. Furthermore, colesevelam intervention alleviated HFD-associated GDM development, improved BAs metabolism, suppressed Fxr, Shp, and Fgf15 activity only in WT mice but not in the Fxr−/− HFD + Colesevelam group and Fxr−/− HFD group. HFD induced GDM and contributed to poor prognosis in GDM parturients through inducing gut microbial dysbiosis and metabolic alteration, especially appeared in BAs profile. Moreover, Fxr pathway participated in regulating HFD-associated gut microbiota disordered BAs metabolites and aggravating GDM in mice.DiscussionModulating gut microbiota and BAs metabolites could be a potential therapeutic strategy in the prevention and treatment of HFD-associated GDM.https://www.frontiersin.org/articles/10.3389/fmicb.2024.1480446/fullhigh-fat dietgestational diabetes mellitusgut microbiotabile acids metabolismFxr pathway
spellingShingle Lei Yao
Xuefei Zhou
Xianqi Jiang
Hao Chen
Yuanliang Li
Xiao Xiong
Yan Tang
Haogang Zhang
Pengfei Qiao
High-fat diet promotes gestational diabetes mellitus through modulating gut microbiota and bile acid metabolism
Frontiers in Microbiology
high-fat diet
gestational diabetes mellitus
gut microbiota
bile acids metabolism
Fxr pathway
title High-fat diet promotes gestational diabetes mellitus through modulating gut microbiota and bile acid metabolism
title_full High-fat diet promotes gestational diabetes mellitus through modulating gut microbiota and bile acid metabolism
title_fullStr High-fat diet promotes gestational diabetes mellitus through modulating gut microbiota and bile acid metabolism
title_full_unstemmed High-fat diet promotes gestational diabetes mellitus through modulating gut microbiota and bile acid metabolism
title_short High-fat diet promotes gestational diabetes mellitus through modulating gut microbiota and bile acid metabolism
title_sort high fat diet promotes gestational diabetes mellitus through modulating gut microbiota and bile acid metabolism
topic high-fat diet
gestational diabetes mellitus
gut microbiota
bile acids metabolism
Fxr pathway
url https://www.frontiersin.org/articles/10.3389/fmicb.2024.1480446/full
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