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Indole-3-Propionic Acid, a Gut Microbiota Metabolite, Protects Against the Development of Postoperative Delirium

OBJECTIVE: The aim was to determine preoperative gut microbiota metabolites that may be associated with postoperative delirium (POD) development in patients and further study in rodents. SUMMARY BACKGROUND DATA: POD occurs in 9% to 50% of older patients undergoing anesthesia/surgery but lacks effect...

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Autores principales: Zhou, Xue, Wu, Xinbo, Wu, Yan, Yang, Liuyue, Shi, Eleanor, Ding, Weihua, Chen, Liang, Shi, Xu, Feng, Xia, Su, Chienwen, You, Zerong, Xia, Jianguo, Chen, Cynthia, Yeliseyev, Vladimir, Bry, Lynn, Xia, Suyun, Huang, Peigen, Meng, Jiawei, Houle, Timothy, Akeju, Oluwaseun, Mao, Jianren, Gerszten, Robert, Chen, Qian, Xie, Zhongcong, Shen, Shiqian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603211/
https://www.ncbi.nlm.nih.gov/pubmed/37185230
http://dx.doi.org/10.1097/SLA.0000000000005886
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author Zhou, Xue
Wu, Xinbo
Wu, Yan
Yang, Liuyue
Shi, Eleanor
Ding, Weihua
Chen, Liang
Shi, Xu
Feng, Xia
Su, Chienwen
You, Zerong
Xia, Jianguo
Chen, Cynthia
Yeliseyev, Vladimir
Bry, Lynn
Xia, Suyun
Huang, Peigen
Meng, Jiawei
Houle, Timothy
Akeju, Oluwaseun
Mao, Jianren
Gerszten, Robert
Chen, Qian
Xie, Zhongcong
Shen, Shiqian
author_facet Zhou, Xue
Wu, Xinbo
Wu, Yan
Yang, Liuyue
Shi, Eleanor
Ding, Weihua
Chen, Liang
Shi, Xu
Feng, Xia
Su, Chienwen
You, Zerong
Xia, Jianguo
Chen, Cynthia
Yeliseyev, Vladimir
Bry, Lynn
Xia, Suyun
Huang, Peigen
Meng, Jiawei
Houle, Timothy
Akeju, Oluwaseun
Mao, Jianren
Gerszten, Robert
Chen, Qian
Xie, Zhongcong
Shen, Shiqian
author_sort Zhou, Xue
collection PubMed
description OBJECTIVE: The aim was to determine preoperative gut microbiota metabolites that may be associated with postoperative delirium (POD) development in patients and further study in rodents. SUMMARY BACKGROUND DATA: POD occurs in 9% to 50% of older patients undergoing anesthesia/surgery but lacks effective treatments or prevention. High-throughput metabolomics using liquid chromatography with tandem mass spectrometry has accelerated disease-related biomarkers discovery. We performed metabolomic studies in humans to identify potential metabolite biomarkers linked to POD and examined potential mechanisms in rodents. METHODS: We performed a prospective observational cohort study to examine the metabolomic changes that were associated with the development of POD. Then the gut microbiota-related metabolomic changes were recapitulated by gut microbiota perturbation in rodents. POD was assessed in mice using a battery of behavioral tests including novel objective test, Y-maze test, open-field test, and buried food test. The mechanisms through which gut microbiota-related metabolomic changes influenced POD were examined using chemogenetics. RESULTS: Indole-3-propionic acid (IPA) is a gut microbiota metabolite that belongs to the indole family. Baseline plasma levels of IPA were significantly inversely correlated with the onset of POD in 103 (17 cases) human individuals. This relationship was validated in preclinical mouse models for POD: reducing IPA levels through gut microbiota perturbation promoted POD-like behavior. More importantly, IPA administration deterred POD-like behavior. Colonization of germ-free mice with mutant Clostridium sporogenes that did not produce IPA-promoted POD-like behavior. Chemogenetic studies revealed that the protective effect of IPA in mice was mediated, in part, by peroxisome proliferator-activated receptor gamma coactivator 1-alpha in hippocampal interneurons. CONCLUSIONS: Gut microbiota-derived IPA is an important molecule implicated in the pathogenesis of POD, which could potentially be harnessed for POD prevention.
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spelling pubmed-106032112023-11-09 Indole-3-Propionic Acid, a Gut Microbiota Metabolite, Protects Against the Development of Postoperative Delirium Zhou, Xue Wu, Xinbo Wu, Yan Yang, Liuyue Shi, Eleanor Ding, Weihua Chen, Liang Shi, Xu Feng, Xia Su, Chienwen You, Zerong Xia, Jianguo Chen, Cynthia Yeliseyev, Vladimir Bry, Lynn Xia, Suyun Huang, Peigen Meng, Jiawei Houle, Timothy Akeju, Oluwaseun Mao, Jianren Gerszten, Robert Chen, Qian Xie, Zhongcong Shen, Shiqian Ann Surg Original Articles OBJECTIVE: The aim was to determine preoperative gut microbiota metabolites that may be associated with postoperative delirium (POD) development in patients and further study in rodents. SUMMARY BACKGROUND DATA: POD occurs in 9% to 50% of older patients undergoing anesthesia/surgery but lacks effective treatments or prevention. High-throughput metabolomics using liquid chromatography with tandem mass spectrometry has accelerated disease-related biomarkers discovery. We performed metabolomic studies in humans to identify potential metabolite biomarkers linked to POD and examined potential mechanisms in rodents. METHODS: We performed a prospective observational cohort study to examine the metabolomic changes that were associated with the development of POD. Then the gut microbiota-related metabolomic changes were recapitulated by gut microbiota perturbation in rodents. POD was assessed in mice using a battery of behavioral tests including novel objective test, Y-maze test, open-field test, and buried food test. The mechanisms through which gut microbiota-related metabolomic changes influenced POD were examined using chemogenetics. RESULTS: Indole-3-propionic acid (IPA) is a gut microbiota metabolite that belongs to the indole family. Baseline plasma levels of IPA were significantly inversely correlated with the onset of POD in 103 (17 cases) human individuals. This relationship was validated in preclinical mouse models for POD: reducing IPA levels through gut microbiota perturbation promoted POD-like behavior. More importantly, IPA administration deterred POD-like behavior. Colonization of germ-free mice with mutant Clostridium sporogenes that did not produce IPA-promoted POD-like behavior. Chemogenetic studies revealed that the protective effect of IPA in mice was mediated, in part, by peroxisome proliferator-activated receptor gamma coactivator 1-alpha in hippocampal interneurons. CONCLUSIONS: Gut microbiota-derived IPA is an important molecule implicated in the pathogenesis of POD, which could potentially be harnessed for POD prevention. Lippincott Williams & Wilkins 2023-12 2023-04-27 /pmc/articles/PMC10603211/ /pubmed/37185230 http://dx.doi.org/10.1097/SLA.0000000000005886 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (https://creativecommons.org/licenses/by/4.0/) (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Original Articles
Zhou, Xue
Wu, Xinbo
Wu, Yan
Yang, Liuyue
Shi, Eleanor
Ding, Weihua
Chen, Liang
Shi, Xu
Feng, Xia
Su, Chienwen
You, Zerong
Xia, Jianguo
Chen, Cynthia
Yeliseyev, Vladimir
Bry, Lynn
Xia, Suyun
Huang, Peigen
Meng, Jiawei
Houle, Timothy
Akeju, Oluwaseun
Mao, Jianren
Gerszten, Robert
Chen, Qian
Xie, Zhongcong
Shen, Shiqian
Indole-3-Propionic Acid, a Gut Microbiota Metabolite, Protects Against the Development of Postoperative Delirium
title Indole-3-Propionic Acid, a Gut Microbiota Metabolite, Protects Against the Development of Postoperative Delirium
title_full Indole-3-Propionic Acid, a Gut Microbiota Metabolite, Protects Against the Development of Postoperative Delirium
title_fullStr Indole-3-Propionic Acid, a Gut Microbiota Metabolite, Protects Against the Development of Postoperative Delirium
title_full_unstemmed Indole-3-Propionic Acid, a Gut Microbiota Metabolite, Protects Against the Development of Postoperative Delirium
title_short Indole-3-Propionic Acid, a Gut Microbiota Metabolite, Protects Against the Development of Postoperative Delirium
title_sort indole-3-propionic acid, a gut microbiota metabolite, protects against the development of postoperative delirium
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603211/
https://www.ncbi.nlm.nih.gov/pubmed/37185230
http://dx.doi.org/10.1097/SLA.0000000000005886
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