窦房结
血管紧张素II
内分泌学
内科学
利钠肽
兴奋剂
受体
纤维化
医学
心钠素
肾素-血管紧张素系统
疾病
激素
化学
心力衰竭
心率
血压
作者
Martin Mackasey,Emmanuel E. Egom,Hailey J. Jansen,Rui Hua,Motahareh Moghtadaei,Yingjie Liu,Jaspreet Kaur,Megan D. McRae,Oleg Bogachev,Sara A. Rafferty,Gibanananda Ray,Adam W. Kirkby,Robert A. Rose
标识
DOI:10.1016/j.jacbts.2018.08.004
摘要
Sinoatrial node (SAN) disease mechanisms are poorly understood, and therapeutic options are limited. Natriuretic peptide(s) (NP) are cardioprotective hormones whose effects can be mediated partly by the NP receptor C (NPR-C). We investigated the role of NPR-C in angiotensin II (Ang II)-mediated SAN disease in mice. Ang II caused SAN disease due to impaired electrical activity in SAN myocytes and increased SAN fibrosis. Strikingly, Ang II treatment in NPR-C-/- mice worsened SAN disease, whereas co-treatment of wild-type mice with Ang II and a selective NPR-C agonist (cANF) prevented SAN dysfunction. NPR-C may represent a new target to protect against the development of Ang II-induced SAN disease.
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