Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1785126556491841536 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10603211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zhouxue indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT wuxinbo indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT wuyan indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT yangliuyue indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT shieleanor indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT dingweihua indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT chenliang indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT shixu indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT fengxia indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT suchienwen indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT youzerong indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT xiajianguo indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT chencynthia indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT yeliseyevvladimir indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT brylynn indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT xiasuyun indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT huangpeigen indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT mengjiawei indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT houletimothy indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT akejuoluwaseun indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT maojianren indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT gersztenrobert indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT chenqian indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT xiezhongcong indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium AT shenshiqian indole3propionicacidagutmicrobiotametaboliteprotectsagainstthedevelopmentofpostoperativedelirium |