Gut-brain axis metabolic pathway regulates antidepressant efficacy of albiflorin

The gut microbiota is increasingly recognized to influence brain function through the gut-brain axis. Albiflorin, an antidepressant natural drug in China with a good safety profile, is difficult to absorb and cannot be detected in the brain after oral administration. Accordingly, the antidepressant...

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Bibliographic Details
Published in:Theranostics 2018-01, Vol.8 (21), p.5945-5959
Main Authors: Zhao, Zhen-Xiong, Fu, Jie, Ma, Shu-Rong, Peng, Ran, Yu, Jin-Bo, Cong, Lin, Pan, Li-Bin, Zhang, Zuo-Guang, Tian, Hui, Che, Chun-Tao, Wang, Yan, Jiang, Jian-Dong
Format: Article
Language:English
Subjects:
Administration, Oral
Animals
Antidepressive Agents - administration & dosage
Antidepressive Agents - metabolism
Antidepressive Agents - pharmacokinetics
Antidepressive Agents - pharmacology
Benzoic Acid - metabolism
Biotransformation
Brain - metabolism
Bridged-Ring Compounds - administration & dosage
Bridged-Ring Compounds - metabolism
Bridged-Ring Compounds - pharmacokinetics
Bridged-Ring Compounds - pharmacology
Carboxylesterase - metabolism
D-Amino-Acid Oxidase - antagonists & inhibitors
Gastrointestinal Microbiome
Metabolic Networks and Pathways
Rats, Sprague-Dawley
Research Paper
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Summary:The gut microbiota is increasingly recognized to influence brain function through the gut-brain axis. Albiflorin, an antidepressant natural drug in China with a good safety profile, is difficult to absorb and cannot be detected in the brain after oral administration. Accordingly, the antidepressant mechanism of albiflorin has not been elucidated clearly. We identified benzoic acid as the characteristic metabolite of albiflorin , then discovered the roles of gut microbiota in the conversion of albiflorin by carboxylesterase Pharmacodynamic and pharmacokinetic studies were performed for the antidepressant activities of albiflorin in animals, and the efficacy of benzoic acid in inhibiting D-amino acid oxidase (DAAO) in brain was further investigated. We validated that gut microbiota transformed albiflorin to benzoic acid, a key metabolite in the intestine that could cross the blood-brain barrier and, as an inhibitor of DAAO in the brain, improved brain function and exerted antidepressant activity . Intestinal carboxylesterase was the crucial enzyme that generated benzoic acid from albiflorin. Additionally, the regulatory effect of albiflorin on the gut microbiota composition was beneficial to alleviate depression. Our findings suggest a novel gut-brain dialogue through intestinal benzoic acid for the treatment of depression and reveal that the gut microbiota may play a causal role in the pathogenesis and treatment of the central nervous system disease.
ISSN:1838-7640
1838-7640
DOI:10.7150/thno.28068