粒体自噬
氧化应激
MFN2型
肾脏疾病
肾
帕金
高脂血症
内分泌学
内科学
肾小球硬化
细胞凋亡
医学
发病机制
线粒体
药理学
化学
糖尿病
自噬
线粒体融合
生物化学
疾病
基因
蛋白尿
帕金森病
线粒体DNA
作者
Xiaoqin Ding,Tunyu Jian,Yanan Gai,Guanting Niu,Yan Liu,Xiuhua Meng,Jing Li,Han Lyu,Bingru Ren,Jian Chen
标识
DOI:10.1021/acs.jafc.1c07795
摘要
As the main factor in the pathogenesis of chronic kidney disease (CKD), the excessive apoptosis of renal tubular epithelial cells (RTECs) and its underlying mechanism of action are worth further investigation. Chicoric acid (CA), a major active constituent of the Uyghur folk medicine chicory, was recorded to possess a renal protective effect. The precise effect of CA on renal tubular injury in obesity-related CKD remains unknown. In the current study, CA was proven to ameliorate metabolic disorders including overweight, hyperglycemia, hyperlipidemia, and hyperuricemia in high fat diet (HFD)-fed mice. Furthermore, the reverse effect of CA on renal histological changes and functional damage was confirmed. In vitro, the alleviation of lipid accumulation and cell apoptosis was observed in palmitic acid (PA)-exposed HK2 cells. Treatment with CA reduced mitochondrial damage and oxidative stress in the renal tubule of HFD-fed mice and PA-treated HK2 cells. Finally, CA was observed to activate the Nrf2 pathway; increase PINK and Parkin expression; and regulate LC3, SQSTM1, Mfn2, and FIS1 expression; therefore, it would improve mitochondrial dynamics and mitophagy to alleviate mitochondrial damage in RTECs of obesity-related CKD. These results may provide fresh insights into the promotion of mitophagy in the prevention and alleviation of obesity-related CKD.
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