安普克
医学
自噬
二甲双胍
白藜芦醇
内科学
心肌病
药理学
蛋白激酶A
AMP活化蛋白激酶
心脏病学
激酶
细胞凋亡
心力衰竭
生物
细胞生物学
胰岛素
生物化学
作者
Ali Molaei,Emad Molaei,Hamid Reza Sadeghnia,A. Wallace Hayes,Gholamreza Karimi
出处
期刊:Life Sciences
[Elsevier BV]
日期:2022-07-27
卷期号:306: 120844-120844
被引量:18
标识
DOI:10.1016/j.lfs.2022.120844
摘要
Cardiovascular diseases (CVDs) are currently the most common cause of morbidity and mortality worldwide. Experimental studies suggest that liver kinase B1 (LKB1) plays an important role in the heart. Several studies have shown that cardiomyocyte-specific LKB1 deletion leads to hypertrophic cardiomyopathy, left ventricular contractile dysfunction, and an increased risk of atrial fibrillation. In addition, the cardioprotective effects of several medicines and natural compounds, including metformin, empagliflozin, bexarotene, and resveratrol, have been reported to be associated with LKB1 activity. LKB1 limits the size of the damaged myocardial area by modifying cellular metabolism, enhancing the antioxidant system, suppressing hypertrophic signals, and inducing mild autophagy, which are all primarily mediated by the AMP-activated protein kinase (AMPK) energy sensor. LKB1 also improves myocardial efficiency by modulating the function of contractile proteins, regulating the expression of electrical channels, and increasing vascular dilatation. Considering these properties, stimulation of LKB1 signaling offers a promising approach in the prevention and treatment of heart diseases.
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