线粒体损伤介导着STING激活,导致肥胖引起的心房动
Zhen Cao1,2,3, Yuntao Fu1,2,3, Yuanjia Ke1,2,3
1Department of Cardiology, Renmin Hospital of Wuhan University, 99 Zhang Zhidong Rd, Wuchang District, Wuhan 430061, China.
概括
肥胖会通过线粒体损伤和干扰素基因刺激器 (STING) 激活增加心房动 (AF) 的风险. 在肥胖大鼠中阻断STING信号减少了AF脆弱性和心脏重塑.
科学领域:
- 心血管研究研究心血管研究
- 分子生物学分子生物学
- 代谢性疾病 代谢性疾病
背景情况:
- 肥胖是心房动 (AF) 的一个主要风险因素.
- 将肥胖与AF联系在一起的确切机制尚不清楚.
- 由线粒体损伤引发的干扰素基因 (STING) 信号的刺激器,与心脏重塑有关.
研究的目的:
- 调查STING信号在肥胖引起的AF中的作用.
- 阐明心脏重塑中STING参与的潜在机制.
主要方法:
- 鼠被养正常或高脂肪饮食 (HFD),并接受STING siRNA或控制siRNA.
- 评估了AF脆弱性,心房STING信号,电力改造和基板改造.
- 评估了线粒体损伤,纤维化,心肌细胞亡和蛋白质变化.
主要成果:
- 肥胖大鼠表现出增加的AF诱导,线粒体损伤和STING通路激活.
- STING激活与心房纤维化,亡和改变的间隙结/离子通道表达相关.
- 在肥胖的老鼠中,STING敲击减轻了AF脆弱性和心脏重塑.
结论:
- 线粒体损伤激活STING信号,促进与肥胖有关的心房重塑和AF.
- 刺痛通路是肥胖症中AF发展的关键调解者.
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