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Conjugated bile acids are nutritionally re-programmable antihypertensive metabolites

BACKGROUND: Hypertension is the largest risk factor affecting global mortality. Despite available medications, uncontrolled hypertension is on the rise, whereby there is an urgent need to develop novel and sustainable therapeutics. Because gut microbiota is now recognized as an important entity in b...

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Autores principales: Chakraborty, Saroj, Lulla, Anju, Cheng, Xi, Yeo, Ji-Youn, Mandal, Juthika, Yang, Tao, Mei, Xue, Saha, Piu, Golonka, Rachel M., Yeoh, Beng San, Mell, Blair, Jia, Wei, Putluri, Vasanta, Piyarathna, Danthasinghe Waduge Badrajee, Putluri, Nagireddy, Sreekumar, Arun, Meyer, Katie, Vijay-Kumar, Matam, Joe, Bina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158603/
https://www.ncbi.nlm.nih.gov/pubmed/37071431
http://dx.doi.org/10.1097/HJH.0000000000003423
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author Chakraborty, Saroj
Lulla, Anju
Cheng, Xi
Yeo, Ji-Youn
Mandal, Juthika
Yang, Tao
Mei, Xue
Saha, Piu
Golonka, Rachel M.
Yeoh, Beng San
Mell, Blair
Jia, Wei
Putluri, Vasanta
Piyarathna, Danthasinghe Waduge Badrajee
Putluri, Nagireddy
Sreekumar, Arun
Meyer, Katie
Vijay-Kumar, Matam
Joe, Bina
author_facet Chakraborty, Saroj
Lulla, Anju
Cheng, Xi
Yeo, Ji-Youn
Mandal, Juthika
Yang, Tao
Mei, Xue
Saha, Piu
Golonka, Rachel M.
Yeoh, Beng San
Mell, Blair
Jia, Wei
Putluri, Vasanta
Piyarathna, Danthasinghe Waduge Badrajee
Putluri, Nagireddy
Sreekumar, Arun
Meyer, Katie
Vijay-Kumar, Matam
Joe, Bina
author_sort Chakraborty, Saroj
collection PubMed
description BACKGROUND: Hypertension is the largest risk factor affecting global mortality. Despite available medications, uncontrolled hypertension is on the rise, whereby there is an urgent need to develop novel and sustainable therapeutics. Because gut microbiota is now recognized as an important entity in blood pressure regulation, one such new avenue is to target the gut-liver axis wherein metabolites are transacted via host-microbiota interactions. Knowledge on which metabolites within the gut-liver axis regulate blood pressure is largely unknown. METHOD: To address this, we analyzed bile acid profiles of human, hypertensive and germ-free rat models and report that conjugated bile acids are inversely correlated with blood pressure in humans and rats. RESULTS: Notably intervening with taurine or tauro-cholic acid rescued bile acid conjugation and reduced blood pressure in hypertensive rats. Subsequently, untargeted metabolomics uncovered altered energy metabolism following conjugation of bile acids as a mechanism alleviating high blood pressure. CONCLUSION: Together this work reveals conjugated bile acids as nutritionally re-programmable anti-hypertensive metabolites.
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spelling pubmed-101586032023-05-05 Conjugated bile acids are nutritionally re-programmable antihypertensive metabolites Chakraborty, Saroj Lulla, Anju Cheng, Xi Yeo, Ji-Youn Mandal, Juthika Yang, Tao Mei, Xue Saha, Piu Golonka, Rachel M. Yeoh, Beng San Mell, Blair Jia, Wei Putluri, Vasanta Piyarathna, Danthasinghe Waduge Badrajee Putluri, Nagireddy Sreekumar, Arun Meyer, Katie Vijay-Kumar, Matam Joe, Bina J Hypertens Original Articles BACKGROUND: Hypertension is the largest risk factor affecting global mortality. Despite available medications, uncontrolled hypertension is on the rise, whereby there is an urgent need to develop novel and sustainable therapeutics. Because gut microbiota is now recognized as an important entity in blood pressure regulation, one such new avenue is to target the gut-liver axis wherein metabolites are transacted via host-microbiota interactions. Knowledge on which metabolites within the gut-liver axis regulate blood pressure is largely unknown. METHOD: To address this, we analyzed bile acid profiles of human, hypertensive and germ-free rat models and report that conjugated bile acids are inversely correlated with blood pressure in humans and rats. RESULTS: Notably intervening with taurine or tauro-cholic acid rescued bile acid conjugation and reduced blood pressure in hypertensive rats. Subsequently, untargeted metabolomics uncovered altered energy metabolism following conjugation of bile acids as a mechanism alleviating high blood pressure. CONCLUSION: Together this work reveals conjugated bile acids as nutritionally re-programmable anti-hypertensive metabolites. Lippincott Williams & Wilkins 2023-06 2023-04-05 /pmc/articles/PMC10158603/ /pubmed/37071431 http://dx.doi.org/10.1097/HJH.0000000000003423 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Articles
Chakraborty, Saroj
Lulla, Anju
Cheng, Xi
Yeo, Ji-Youn
Mandal, Juthika
Yang, Tao
Mei, Xue
Saha, Piu
Golonka, Rachel M.
Yeoh, Beng San
Mell, Blair
Jia, Wei
Putluri, Vasanta
Piyarathna, Danthasinghe Waduge Badrajee
Putluri, Nagireddy
Sreekumar, Arun
Meyer, Katie
Vijay-Kumar, Matam
Joe, Bina
Conjugated bile acids are nutritionally re-programmable antihypertensive metabolites
title Conjugated bile acids are nutritionally re-programmable antihypertensive metabolites
title_full Conjugated bile acids are nutritionally re-programmable antihypertensive metabolites
title_fullStr Conjugated bile acids are nutritionally re-programmable antihypertensive metabolites
title_full_unstemmed Conjugated bile acids are nutritionally re-programmable antihypertensive metabolites
title_short Conjugated bile acids are nutritionally re-programmable antihypertensive metabolites
title_sort conjugated bile acids are nutritionally re-programmable antihypertensive metabolites
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158603/
https://www.ncbi.nlm.nih.gov/pubmed/37071431
http://dx.doi.org/10.1097/HJH.0000000000003423
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