氧化应激
安普克
血管紧张素II
心脏纤维化
炎症
纤维化
化学
心力衰竭
心室重构
内科学
药理学
内分泌学
蛋白激酶A
医学
激酶
生物化学
受体
作者
Yao Du,Jibo Han,Haixia Zhang,Jianjiang Xu,Liqin Jiang,Weihong Ge
标识
DOI:10.1097/fjc.0000000000000713
摘要
Heart failure characterized by cardiac remodeling is a global problem. Angiotensin II (Ang II) induces cardiac inflammation and oxidative stress, which also is implicated in the pathophysiology of adverse collagen accumulation-induced remodeling. Kaempferol (KPF), a kind of flavonoid compounds, is capable of anti-inflammatory and antioxidant activities. However, the target of KPF still remains blurred. In this study, we investigated the effect of KPF on Ang II-induced collagen accumulation and explored the underlying mechanisms. Our results suggested that KPF prevented Ang II-induced cardiac fibrosis and dysfunction, in mice challenged with subcutaneous injection of Ang II. In culture cells, KPF significantly reduced Ang II-induced collagen accumulation. Furthermore, KPF remarkably decreased inflammation and oxidative stress in Ang II-stimulated cardiac fibroblasts by modulating NF-κB/mitogen-activated protein kinase and AMPK/Nrf2 pathways.
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