首页> 美国卫生研究院文献>Nutrients >Green Tea Polyphenols Mimicking the Effects of Dietary Restriction Ameliorate High-Fat Diet-Induced Kidney Injury via Regulating Autophagy Flux
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Green Tea Polyphenols Mimicking the Effects of Dietary Restriction Ameliorate High-Fat Diet-Induced Kidney Injury via Regulating Autophagy Flux

机译:绿茶多酚模仿饮食限制的影响通过调节自噬通量减轻高脂饮食引起的肾脏损伤

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摘要

Epidemiological and experimental studies reveal that Western dietary patterns contribute to chronic kidney disease, whereas dietary restriction (DR) or dietary polyphenols such as green tea polyphenols (GTPs) can ameliorate the progression of kidney injury. This study aimed to investigate the renal protective effects of GTPs and explore the underlying mechanisms. Sixty Wistar rats were randomly divided into 6 groups: standard diet (STD), DR, high-fat diet (HFD), and three diets plus 200 mg/kg(bw)/day GTPs, respectively. After 18 weeks, HFD group exhibited renal injuries by increased serum cystatin C levels and urinary N-acetyl-β-d-glucosaminidase activity, which can be ameliorated by GTPs. Meanwhile, autophagy impairment as denoted by autophagy-lysosome related proteins, including LC3-II, Beclin-1, p62, cathepsin B, cathepsin D and LAMP-1, was observed in HFD group, whereas DR or GTPs promoted renal autophagy activities and GTPs ameliorated HFD-induced autophagy impairment. In vitro, autophagy flux suppression was detected in palmitic acid (PA)-treated human proximal tubular epithelial cells (HK-2), which was ameliorated by epigallocatechin-3-gallate (EGCG). Furthermore, GTPs (or EGCG) elevated phosphorylation of AMP-activated protein kinase in the kidneys of HFD-treated rats and in PA-treated HK-2 cells. These findings revealed that GTPs mimic the effects of DR to induce autophagy and exert a renal protective effect by alleviating HFD-induced autophagy suppression.
机译:流行病学和实验研究表明,西方饮食模式可导致慢性肾脏疾病,而饮食限制(DR)或饮食中的多酚(例如绿茶多酚)可改善肾脏损伤的进程。这项研究旨在调查GTP的肾脏保护作用并探讨其潜在机制。 60只Wistar大鼠随机分为6组:标准饮食(STD),DR,高脂饮食(HFD)和3种饮食加200 mg / kg(bw)/天GTP。 18周后,HFD组的血清半胱氨酸蛋白酶抑制剂C水平升高和尿中N-乙酰基-β-d-氨基葡萄糖苷酶活性升高,肾脏损害可被GTP改善。同时,在HFD组中观察到以LC3-II,Beclin-1,p62,组织蛋白酶B,组织蛋白酶D和LAMP-1等自噬溶酶体相关蛋白表示的自噬损伤,而DR或GTP促进了肾脏自噬活性和GTP。改善了HFD诱导的自噬功能障碍。在体外,在棕榈酸(PA)处理的人近端肾小管上皮细胞(HK-2)中检测到自噬通量抑制,其被表没食子儿茶素-3-没食子酸酯(EGCG)改善。此外,在HFD治疗的大鼠肾脏和PA治疗的HK-2细胞中,GTP(或EGCG)提高了AMP激活的蛋白激酶的磷酸化。这些发现表明,GTP通过减轻HFD诱导的自噬抑制作用模仿DR诱导自噬的作用并发挥肾脏保护作用。

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