辛伐他汀
医学
心力衰竭
氧化应激
药理学
载脂蛋白E
载脂蛋白B
内科学
心肌梗塞
胆固醇
疾病
作者
Yanfang Yang,Ke Feng,Liying Yuan,Yuxin Liu,Mengying Zhang,Kaimin Guo,Zequn Yin,Wenjia Wang,Shuiping Zhou,He Sun,Kaijing Yan,Xijun Yan,Xuerui Wang,Yajun Duan,Yunhui Hu,Jihong Han
标识
DOI:10.1016/j.apsb.2022.11.012
摘要
) mice and investigated the effect of CDDP or CDDP plus a low dose of simvastatin on the heart failure. CDDP or CDDP plus a low dose of simvastatin inhibited heart injury by multiple actions including anti-myocardial dysfunction and anti-fibrosis. Mechanistically, both Wnt and lysine-specific demethylase 4A (KDM4A) pathways were significantly activated in mice with heart injury. Conversely, CDDP or CDDP plus a low dose of simvastatin inhibited Wnt pathway by markedly up-regulating expression of Wnt inhibitors. While the anti-inflammation and anti-oxidative stress by CDDP were achieved by inhibiting KDM4A expression and activity. In addition, CDDP attenuated simvastatin-induced myolysis in skeletal muscle. Taken together, our study suggests that CDDP or CDDP plus a low dose of simvastatin can be an effective therapy to reduce hypercholesterolemia/atherosclerosis-induced heart failure.
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