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

Author:

Zhou Xue1,Wu Xinbo12,Wu Yan3,Yang Liuyue1,Shi Eleanor4,Ding Weihua1,Chen Liang5,Shi Xu6,Feng Xia3,Su Chienwen7,You Zerong1,Xia Jianguo8,Chen Cynthia1,Yeliseyev Vladimir9,Bry Lynn9,Xia Suyun1,Huang Peigen10,Meng Jiawei1,Houle Timothy1,Akeju Oluwaseun1,Mao Jianren1,Gerszten Robert6,Chen Qian1112,Xie Zhongcong1,Shen Shiqian1

Affiliation:

1. Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA

2. Department of Orthopedics, Shanghai Tenth Hospital, Tongji University School of Medicine, Shanghai

3. Department of Anesthesiology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China

4. Dana Farber Cancer Institute, Harvard Medical School, Boston, MA

5. Center for Discovery and Innovation, Hackensack Health Care, Nutley, NJ

6. Department of Cardiovascular Medicine, Beth Israel Deaconess Medical Center

7. Department of Pediatrics, Massachusetts General Hospital, Harvard Medical School, Boston, MA

8. Department of Parasitology, McGill University, Montreal, Canada

9. Department of Pathology, Brigham and Women’s Hospital

10. The Steele Lab, Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston

11. McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA

12. Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China

Abstract

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Surgery

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