Akkermansia muciniphila prevents cold-related atrial fibrillation in rats by modulation of TMAO induced cardiac pyroptosis

被引:70
作者
Luo, Yingchun [1 ]
Zhang, Yun [1 ,7 ]
Han, Xuejie [1 ]
Yuan, Yue [1 ]
Zhou, Yun [1 ]
Gao, Yunlong [1 ]
Yu, Hui [1 ]
Zhang, Jiawei [2 ]
Shi, Yiya [7 ]
Duan, Yu [1 ]
Zhao, Xinbo [1 ]
Yan, Sen [1 ]
Hao, Hongting [1 ]
Dai, Chenguang [1 ]
Zhao, Shiqi [1 ]
Shi, Jing [1 ]
Li, Wenpeng [1 ]
Zhang, Song [1 ]
Xu, Wei [1 ]
Fang, Ning [1 ]
Gong, Yongtai [1 ,8 ]
Li, Yue [1 ,3 ,4 ,5 ,6 ,8 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Cardiol, Harbin 150001, Peoples R China
[2] Qingdao Cent Hosp, Dept Cardiol, Qingdao, Peoples R China
[3] Harbin Med Univ, NHC Key Lab Cell Translat, Heilongjiang 150001, Peoples R China
[4] Harbin Med Univ, Key Lab Hepatosplen Surg, Minist Educ, Harbin 150001, Peoples R China
[5] Harbin Med Univ, Key Lab Cardiac Dis & Heart Failure, Harbin 150001, Peoples R China
[6] Heilongjiang Key Lab Metab Disorder & Canc Related, Harbin 150081, Peoples R China
[7] Southern Med Univ, Zhujiang Hosp, Microbiome Med Ctr, Div Lab Med, Guangzhou, Guangdong, Peoples R China
[8] Harbin Med Univ, Affiliated Hosp 1, Dept Cardiol, Youzheng St 23, Harbin 150001, Peoples R China
基金
中国国家自然科学基金;
关键词
Cold; Atrial fibrillation; Gut microbiota; Akkermansia muciniphila; TMAO; TRIMETHYLAMINE-N-OXIDE; GUT MICROBIOTA; SEASONAL-VARIATION; HEART; TEMPERATURE; HOMEOSTASIS; METABOLISM; MACROPHAGE; CONVERSION; FREQUENCY;
D O I
10.1016/j.ebiom.2022.104087
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Cold exposure is one of the most important risk factors for atrial fibrillation (AF), and closely related to the poor prognosis of AF patients. However, the mechanisms underlying cold-related AF are poorly understood. Methods Various techniques including 16S rRNA gene sequencing, fecal microbiota transplantation, and electrophysiological examination were used to determine whether gut microbiota dysbiosis promotes cold-related AF. Metabonomics were performed to investigate changes in fecal trimethylamine (TMA) and plasma trimethylamine N-oxide (TMAO) during cold exposure. The detailed mechanism underlying cold-related AF were examined in vitro. Transgenic mice were constructed to explore the role of pyroptosis in cold-related AF. The human cohort was used to evaluate the correlation between A. muciniphila and cold-related AF. Findings We found that cold exposure caused elevated susceptibility to AF and reduced abundance of Akkermansia muciniphila (A. muciniphila) in rats. Intriguingly, oral supplementation of A. muciniphila ameliorated the pro-AF property induced by cold exposure. Mechanistically, cold exposure disrupted the A. muciniphila, by which elevated the level of trimethylamine N-oxide (TMAO) through modulation of the microbial enzymes involved in trimethylamine (TMA) synthesis. Correspondingly, progressively increased plasma TMAO levels were validated in human subjects during cold weather. Raised TMAO enhanced the infiltration of M1 macrophages in atria and increased the expression of Casp1-p20 and cleaved-GSDMD, ultimately causing atrial structural remodeling. Furthermore, the mice with conditional deletion of caspase1 exhibited resistance to cold-related AF. More importantly, a cross-sectional clinical study revealed that the reduction of A. muciniphila abundance was an independent risk factor for cold-related AF in human subjects. Interpretation Our findings revealed a novel causal role of aberrant gut microbiota and metabolites in pathogenesis of cold-related AF, which raises the possibility of selectively targeting microbiota and microbial metabolites as a potential therapeutic strategy for cold-related AF. Copyright (C) 2022 The Authors. Published by Elsevier B.V.
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页数:17
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