自噬
安普克
脂毒性
山奈酚
PI3K/AKT/mTOR通路
细胞生物学
化学
磷酸化
程序性细胞死亡
蛋白激酶B
活力测定
癌症研究
细胞凋亡
蛋白激酶A
信号转导
生物
内分泌学
生物化学
胰岛素
槲皮素
胰岛素抵抗
抗氧化剂
作者
Ritu Varshney,Sumeet Gupta,Partha Roy
标识
DOI:10.1016/j.mce.2017.02.033
摘要
Lipotoxicity of pancreatic β-cells is the pathological manifestation of obesity-linked type II diabetes. We intended to determine the cytoprotective effect of kaempferol on pancreatic β-cells undergoing apoptosis in palmitic acid (PA)-stressed condition. The data showed that kaempferol treatment increased cell viability and anti-apoptotic activity in PA-stressed RIN-5F cells and murine pancreatic islets. Furthermore, kaempferol's ability to instigate autophagy was illustrated by MDC-LysoTracker red staining and TEM analysis which corroborated well with the observed increase in LC3 puncta and LC3-II protein expressions along with the concomitant decline in p62 expression. Apart from this, the data showed that kaempferol up/down-regulates AMPK/mTOR phosphorylation respectively. Subsequently, upon inhibition of AMPK phosphorylation by AMPK inhibitors, kaempferol-mediated autophagy was abolished which further led to the decline in β-cell survival. Such observations collectively lead to the conclusion that, kaempferol exerts its cytoprotective role against lipotoxicity by activation of autophagy via AMPK/mTOR pathway.
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