Dataset Information

CB1R-stabilized NLRP3 inflammasome drives antipsychotics cardiotoxicity.

ABSTRACT: Long-term use of antipsychotics is a common cause of myocardial injury and even sudden cardiac deaths that often lead to drug withdrawn or discontinuation. Mechanisms underlying antipsychotics cardiotoxicity remain largely unknown. Herein we performed RNA sequencing and found that NLRP3 inflammasome-mediated pyroptosis contributed predominantly to multiple antipsychotics cardiotoxicity. Pyroptosis-based small-molecule compound screen identified cannabinoid receptor 1 (CB1R) as an upstream regulator of the NLRP3 inflammasome. Mechanistically, antipsychotics competitively bond to the CB1R and led to CB1R translocation to the cytoplasm, where CB1R directly interacted with NLRP3 inflammasome via amino acid residues 177-209, rendering stabilization of the inflammasome. Knockout of Cb1r significantly alleviated antipsychotic-induced cardiomyocyte pyroptosis and cardiotoxicity. Multi-organ-based investigation revealed no additional toxicity of newer CB1R antagonists. In authentic human cases, the expression of CB1R and NLRP3 inflammasome positively correlated with antipsychotics-induced cardiotoxicity. These results suggest that CB1R is a potent regulator of the NLRP3 inflammsome-mediated pyroptosis and small-molecule inhibitors targeting the CB1R/NLRP3 signaling represent attractive approaches to rescue cardiac side effects of antipsychotics.

SUBMITTER: Li L

PROVIDER: S-EPMC9225989 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

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CB1R-stabilized NLRP3 inflammasome drives antipsychotics cardiotoxicity.

Li Liliang L Gao Pan P Tang Xinru X Liu Zheng Z Cao Mengying M Luo Ruoyu R Li Xiaoqing X Wang Jing J Lin Xinyi X Peng Chao C Li Zhihong Z Zhang Jianhua J Zhang Xian X Cao Zhonglian Z Zou Yunzeng Y Jin Li L

Signal transduction and targeted therapy 20220624 1

Long-term use of antipsychotics is a common cause of myocardial injury and even sudden cardiac deaths that often lead to drug withdrawn or discontinuation. Mechanisms underlying antipsychotics cardiotoxicity remain largely unknown. Herein we performed RNA sequencing and found that NLRP3 inflammasome-mediated pyroptosis contributed predominantly to multiple antipsychotics cardiotoxicity. Pyroptosis-based small-molecule compound screen identified cannabinoid receptor 1 (CB1R) as an upstream regula ...[more]

PMID: 35739093

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CB1R-stabilized NLRP3 inflammasome drives antipsychotics cardiotoxicity.

Publications

CB1R-stabilized NLRP3 inflammasome drives antipsychotics cardiotoxicity.

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