Gender differences in the bile acid profiles of APP/PS1 transgenic AD mice

Alzheimer's disease (AD) is a neurodegenerative disease and presents in the accumulation of amyloid and neurofibrillary tangle. The association between modulations of gut symbiotic microbes with neurological disease via bidirectional gut-brain axis has been well documented. Bile acid (BA) pools...

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Main Authors: Wu, Junfang, Zhu, Xuehang, Lin, Hong, Chen, Ziliang, Tang, Huiru, Wang, Yulan
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/143838
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1438382020-11-01T05:15:05Z Gender differences in the bile acid profiles of APP/PS1 transgenic AD mice Wu, Junfang Zhu, Xuehang Lin, Hong Chen, Ziliang Tang, Huiru Wang, Yulan Lee Kong Chian School of Medicine (LKCMedicine) Singapore Phenome Center Science::Medicine Bile Acid Gender Difference Alzheimer's disease (AD) is a neurodegenerative disease and presents in the accumulation of amyloid and neurofibrillary tangle. The association between modulations of gut symbiotic microbes with neurological disease via bidirectional gut-brain axis has been well documented. Bile acid (BA) pools in the enterohepatic circulation could be valuable for probing complex biochemical interactions between host and their symbiotic microbiota. Herein we investigated the levels of 28 BAs in several compartments in enterohepatic circulation (including jejunal, ileum, cecum, colon and feces, plasma and liver tissue) by employing an APP/PS1 induced transgenic AD mouse model. We found that BA profiles in AD mice were gender specific. We observed decreased levels of taurine-conjugated primary BAs (TUDCA, TCA, T-α-MCA and T-β-MCA) and increased levels of secondary BA (iso-DCA) in plasma and liver extracts for female AD transgenic mice. In contrast, increased levels of TDCA in liver extracts and decreased levels of T-β-MCA in jejunal content were noted in male AD mice. These observations suggested that perturbations of BA profiles in AD mice displayed clear gender variations. Our study highlighted the roles of gut microbiota on neurodegenerative disease, which could be gender specific. Accepted version 2020-09-25T05:09:53Z 2020-09-25T05:09:53Z 2020 Journal Article Wu, J., Zhu, X., Lin, H., Chen, Z., Tang, H., & Wang, Y. (2020). Gender differences in the bile acid profiles of APP/PS1 transgenic AD mice. Brain Research Bulletin, 161, 116–126. doi:10.1016/j.brainresbull.2020.05.003 0361-9230 https://hdl.handle.net/10356/143838 10.1016/j.brainresbull.2020.05.003 32437836 161 116 126 en Brain research bulletin © 2020 Elsevier Inc. All rights reserved. This paper was published in Brain research bulletin and is made available with permission of Elsevier Inc. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Medicine
Bile Acid
Gender Difference
spellingShingle Science::Medicine
Bile Acid
Gender Difference
Wu, Junfang
Zhu, Xuehang
Lin, Hong
Chen, Ziliang
Tang, Huiru
Wang, Yulan
Gender differences in the bile acid profiles of APP/PS1 transgenic AD mice
description Alzheimer's disease (AD) is a neurodegenerative disease and presents in the accumulation of amyloid and neurofibrillary tangle. The association between modulations of gut symbiotic microbes with neurological disease via bidirectional gut-brain axis has been well documented. Bile acid (BA) pools in the enterohepatic circulation could be valuable for probing complex biochemical interactions between host and their symbiotic microbiota. Herein we investigated the levels of 28 BAs in several compartments in enterohepatic circulation (including jejunal, ileum, cecum, colon and feces, plasma and liver tissue) by employing an APP/PS1 induced transgenic AD mouse model. We found that BA profiles in AD mice were gender specific. We observed decreased levels of taurine-conjugated primary BAs (TUDCA, TCA, T-α-MCA and T-β-MCA) and increased levels of secondary BA (iso-DCA) in plasma and liver extracts for female AD transgenic mice. In contrast, increased levels of TDCA in liver extracts and decreased levels of T-β-MCA in jejunal content were noted in male AD mice. These observations suggested that perturbations of BA profiles in AD mice displayed clear gender variations. Our study highlighted the roles of gut microbiota on neurodegenerative disease, which could be gender specific.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Wu, Junfang
Zhu, Xuehang
Lin, Hong
Chen, Ziliang
Tang, Huiru
Wang, Yulan
format Article
author Wu, Junfang
Zhu, Xuehang
Lin, Hong
Chen, Ziliang
Tang, Huiru
Wang, Yulan
author_sort Wu, Junfang
title Gender differences in the bile acid profiles of APP/PS1 transgenic AD mice
title_short Gender differences in the bile acid profiles of APP/PS1 transgenic AD mice
title_full Gender differences in the bile acid profiles of APP/PS1 transgenic AD mice
title_fullStr Gender differences in the bile acid profiles of APP/PS1 transgenic AD mice
title_full_unstemmed Gender differences in the bile acid profiles of APP/PS1 transgenic AD mice
title_sort gender differences in the bile acid profiles of app/ps1 transgenic ad mice
publishDate 2020
url https://hdl.handle.net/10356/143838
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