Dynamical alterations of brain function and gut microbiome in weight loss

ObjectiveIntermittent energy restriction (IER) is an effective weight loss strategy. However, little is known about the dynamic effects of IER on the brain-gut-microbiome axis.MethodsIn this study, a total of 25 obese individuals successfully lost weight after a 2-month IER intervention. FMRI was us...

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Main Authors: Jing Zhou, Xiaoling Wu, Tianyuan Xiang, Fei Liu, Hui Gao, Li Tong, Bin Yan, Zhonglin Li, Chi Zhang, Linyuan Wang, Lei Ou, Zhongxia Li, Wen Wang, Tingting Yang, Fengyun Li, Huimin Ma, Xiaojuan Zhao, Na Mi, Ziya Yu, Canhui Lan, Qi Wang, Hao Li, Liming Wang, Xiaoning Wang, Yongli Li, Qiang Zeng
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-12-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcimb.2023.1269548/full
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author Jing Zhou
Xiaoling Wu
Tianyuan Xiang
Fei Liu
Hui Gao
Li Tong
Bin Yan
Zhonglin Li
Chi Zhang
Linyuan Wang
Lei Ou
Zhongxia Li
Zhongxia Li
Wen Wang
Tingting Yang
Fengyun Li
Huimin Ma
Xiaojuan Zhao
Na Mi
Ziya Yu
Canhui Lan
Qi Wang
Hao Li
Liming Wang
Xiaoning Wang
Yongli Li
Qiang Zeng
author_facet Jing Zhou
Xiaoling Wu
Tianyuan Xiang
Fei Liu
Hui Gao
Li Tong
Bin Yan
Zhonglin Li
Chi Zhang
Linyuan Wang
Lei Ou
Zhongxia Li
Zhongxia Li
Wen Wang
Tingting Yang
Fengyun Li
Huimin Ma
Xiaojuan Zhao
Na Mi
Ziya Yu
Canhui Lan
Qi Wang
Hao Li
Liming Wang
Xiaoning Wang
Yongli Li
Qiang Zeng
author_sort Jing Zhou
collection DOAJ
description ObjectiveIntermittent energy restriction (IER) is an effective weight loss strategy. However, little is known about the dynamic effects of IER on the brain-gut-microbiome axis.MethodsIn this study, a total of 25 obese individuals successfully lost weight after a 2-month IER intervention. FMRI was used to determine the activity of brain regions. Metagenomic sequencing was performed to identify differentially abundant gut microbes and pathways in from fecal samples.ResultsOur results showed that IER longitudinally reduced the activity of obese-related brain regions at different timepoints, including the inferior frontal orbital gyrus in the cognitive control circuit, the putamen in the emotion and learning circuit, and the anterior cingulate cortex in the sensory circuit. IER longitudinally reduced E. coli abundance across multiple timepoints while elevating the abundance of obesity-related Faecalibacterium prausnitzii, Parabacteroides distasonis, and Bacterokles uniformis. Correlation analysis revealed longitudinally correlations between gut bacteria abundance alterations and brain activity changes.ConclusionsThere was dynamical alteration of BGM axis (the communication of E. coli with specific brain regions) during the weight loss under the IER.
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spelling doaj.art-bf08aeb603c747949f81214dda6435892023-12-20T07:47:45ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882023-12-011310.3389/fcimb.2023.12695481269548Dynamical alterations of brain function and gut microbiome in weight lossJing Zhou0Xiaoling Wu1Tianyuan Xiang2Fei Liu3Hui Gao4Li Tong5Bin Yan6Zhonglin Li7Chi Zhang8Linyuan Wang9Lei Ou10Zhongxia Li11Zhongxia Li12Wen Wang13Tingting Yang14Fengyun Li15Huimin Ma16Xiaojuan Zhao17Na Mi18Ziya Yu19Canhui Lan20Qi Wang21Hao Li22Liming Wang23Xiaoning Wang24Yongli Li25Qiang Zeng26Henan Provincial Research Center of Clinical Medicine of Nephropathy, Henan Provincial People’s Hospital, Zhengzhou University People’s Hospital, Henan University People’s Hospital, Zhengzhou, ChinaDepartment of Nuclear Medicine, Henan Key Laboratory of Chronic Disease Health Management, Henan Provincial People’s Hospital, Zhengzhou University People’s Hospital, Zhengzhou, Henan, ChinaHealth Management Institute, The Second Medical Center & National Clinical Research Center for Geriatric Diseases, Chinese People's Liberation Army (PLA) General Hospital, Beijing, ChinaInstitute of Microbiology, Chinese Academy of Sciences, Beijing, ChinaHenan Key Laboratory of Imaging and Intelligent Processing, People’s Liberation Army (PLA) Strategic Support Force Information Engineering University, Zhengzhou, Henan, ChinaHenan Key Laboratory of Imaging and Intelligent Processing, People’s Liberation Army (PLA) Strategic Support Force Information Engineering University, Zhengzhou, Henan, ChinaHenan Key Laboratory of Imaging and Intelligent Processing, People’s Liberation Army (PLA) Strategic Support Force Information Engineering University, Zhengzhou, Henan, ChinaDepartment of Radiology, Henan Provincial People’s Hospital, Zhengzhou, Henan, ChinaHenan Key Laboratory of Imaging and Intelligent Processing, People’s Liberation Army (PLA) Strategic Support Force Information Engineering University, Zhengzhou, Henan, ChinaHenan Key Laboratory of Imaging and Intelligent Processing, People’s Liberation Army (PLA) Strategic Support Force Information Engineering University, Zhengzhou, Henan, ChinaHealth Management Institute, The Second Medical Center & National Clinical Research Center for Geriatric Diseases, Chinese People's Liberation Army (PLA) General Hospital, Beijing, ChinaBYHEALTH Institute of Nutrition & Health, BYHEALTH Co. Ltd, Guangzhou, Guangdong, ChinaDepartment of Cardiology, Sun Yat-sen Memorial Hospital of Sun Yat-sen University, Guangzhou, Guangdong, ChinaDepartment of Nutrition, Henan Provincial People’s Hospital, Zhengzhou University People’s Hospital, Henan, Zhengzhou, ChinaDepartment of Nutrition, Henan Provincial People’s Hospital, Zhengzhou University People’s Hospital, Henan, Zhengzhou, China0Department of Health Management, Henan Provincial People’s Hospital, Zhengzhou University People’s Hospital, Henan University People’s Hospital, Zhengzhou, Henan, China0Department of Health Management, Henan Provincial People’s Hospital, Zhengzhou University People’s Hospital, Henan University People’s Hospital, Zhengzhou, Henan, China0Department of Health Management, Henan Provincial People’s Hospital, Zhengzhou University People’s Hospital, Henan University People’s Hospital, Zhengzhou, Henan, China0Department of Health Management, Henan Provincial People’s Hospital, Zhengzhou University People’s Hospital, Henan University People’s Hospital, Zhengzhou, Henan, ChinaHenan Key Laboratory of Imaging and Intelligent Processing, People’s Liberation Army (PLA) Strategic Support Force Information Engineering University, Zhengzhou, Henan, China1Beijing Rexinchang Biotechnology Research Institute Co. Ltd, Beijing, China2Cuiying Biomedical Research Center, Lanzhou University Second Hospital, Lanzhou, Gansu, China3Department of Health Management, Fuwai Central China Cardiovascular Hospital, Zhengzhou, ChinaInstitute of Microbiology, Chinese Academy of Sciences, Beijing, China4The Institute of Geriatrics, The State Clinic Center for Geriatrics & The State Key Laboratory of Kidney, The People’s Liberation Army (PLA) General Hospital, Beijing, China5Department of Health Management, Henan Key Laboratory of Chronic Disease Management, Henan Provincial People’s Hospital, Zhengzhou University People’s Hospital, Henan University People’s Hospital, Zhengzhou, Henan, ChinaHealth Management Institute, The Second Medical Center & National Clinical Research Center for Geriatric Diseases, Chinese People's Liberation Army (PLA) General Hospital, Beijing, ChinaObjectiveIntermittent energy restriction (IER) is an effective weight loss strategy. However, little is known about the dynamic effects of IER on the brain-gut-microbiome axis.MethodsIn this study, a total of 25 obese individuals successfully lost weight after a 2-month IER intervention. FMRI was used to determine the activity of brain regions. Metagenomic sequencing was performed to identify differentially abundant gut microbes and pathways in from fecal samples.ResultsOur results showed that IER longitudinally reduced the activity of obese-related brain regions at different timepoints, including the inferior frontal orbital gyrus in the cognitive control circuit, the putamen in the emotion and learning circuit, and the anterior cingulate cortex in the sensory circuit. IER longitudinally reduced E. coli abundance across multiple timepoints while elevating the abundance of obesity-related Faecalibacterium prausnitzii, Parabacteroides distasonis, and Bacterokles uniformis. Correlation analysis revealed longitudinally correlations between gut bacteria abundance alterations and brain activity changes.ConclusionsThere was dynamical alteration of BGM axis (the communication of E. coli with specific brain regions) during the weight loss under the IER.https://www.frontiersin.org/articles/10.3389/fcimb.2023.1269548/fullbrain-gut-microbiome axisweight lossfunctional magnetic resonance imagingintermittent energy restrictionmetagenomics
spellingShingle Jing Zhou
Xiaoling Wu
Tianyuan Xiang
Fei Liu
Hui Gao
Li Tong
Bin Yan
Zhonglin Li
Chi Zhang
Linyuan Wang
Lei Ou
Zhongxia Li
Zhongxia Li
Wen Wang
Tingting Yang
Fengyun Li
Huimin Ma
Xiaojuan Zhao
Na Mi
Ziya Yu
Canhui Lan
Qi Wang
Hao Li
Liming Wang
Xiaoning Wang
Yongli Li
Qiang Zeng
Dynamical alterations of brain function and gut microbiome in weight loss
Frontiers in Cellular and Infection Microbiology
brain-gut-microbiome axis
weight loss
functional magnetic resonance imaging
intermittent energy restriction
metagenomics
title Dynamical alterations of brain function and gut microbiome in weight loss
title_full Dynamical alterations of brain function and gut microbiome in weight loss
title_fullStr Dynamical alterations of brain function and gut microbiome in weight loss
title_full_unstemmed Dynamical alterations of brain function and gut microbiome in weight loss
title_short Dynamical alterations of brain function and gut microbiome in weight loss
title_sort dynamical alterations of brain function and gut microbiome in weight loss
topic brain-gut-microbiome axis
weight loss
functional magnetic resonance imaging
intermittent energy restriction
metagenomics
url https://www.frontiersin.org/articles/10.3389/fcimb.2023.1269548/full
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