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肾康注射液对高糖诱导肾小管细胞衰老的预防作用。

Preventive effect of Shenkang injection against high glucose-induced senescence of renal tubular cells.

机构信息

Department of Nephrology, Daping Hospital, Army Medical University, Chongqing, 400042, China.

出版信息

Front Med. 2019 Apr;13(2):267-276. doi: 10.1007/s11684-017-0586-8. Epub 2018 Apr 25.

Abstract

Shenkang injection (SKI) is a classic prescription composed of Radix Astragali, rhubarb, Astragalus, Safflower, and Salvia. This treatment was approved by the State Food and Drug Administration of China in 1999 for treatment of chronic kidney diseases based on good efficacy and safety. This study aimed to investigate the protective effect of SKI against high glucose (HG)-induced renal tubular cell senescence and its underlying mechanism. Primary renal proximal tubule epithelial cells were cultured in (1) control medium (control group), medium containing 5 mmol/L glucose; (2) mannitol medium (mannitol group), medium containing 5 mmol/L glucose, and 25 mmol/L mannitol; (3) HG medium (HG group) containing 30 mmol/L glucose; (4) SKI treatment at high (200 mg/L), medium (100 mg/L), or low (50 mg/L) concentration in HG medium (HG + SKI group); or (5) 200 mg/L SKI treatment in control medium (control + SKI group) for 72 h. HG-induced senescent cells showed the emergence of senescence associated heterochromatin foci, up-regulation of P16 and cyclin D1, increased senescence-associated β-galactosidase activity, and elevated expression of membrane decoy receptor 2. SKI treatment potently prevented these changes in a dose-independent manner. SKI treatment prevented HG-induced up-regulation of pro-senescence molecule mammalian target of rapamycin and p66Shc and down-regulation of anti-senescence molecules klotho, sirt1, and peroxisome proliferator-activated receptor-g in renal tubular epithelial cells. SKI may be a novel strategy for protecting against HG-induced renal tubular cell senescence in treatment of diabetic nephropathy.

摘要

肾康注射液(SKI)是一种经典的方剂,由黄芪、大黄、黄芪、红花和丹参组成。该治疗方法于 1999 年经中国国家食品药品监督管理局批准,基于良好的疗效和安全性,用于治疗慢性肾脏病。本研究旨在探讨 SKI 对高糖(HG)诱导的肾小管细胞衰老的保护作用及其机制。原代肾近端小管上皮细胞在(1)对照培养基(对照组)、含 5mmol/L 葡萄糖的培养基;(2)甘露醇培养基(甘露醇组)、含 5mmol/L 葡萄糖和 25mmol/L 甘露醇的培养基;(3)含 30mmol/L 葡萄糖的 HG 培养基(HG 组);(4)HG 培养基中高(200mg/L)、中(100mg/L)、低(50mg/L)浓度 SKI 处理(HG+SKI 组);或(5)200mg/L SKI 在对照培养基中处理(对照+SKI 组)72h。HG 诱导的衰老细胞出现衰老相关异染色质焦点,P16 和细胞周期蛋白 D1 上调,衰老相关β-半乳糖苷酶活性增加,膜诱饵受体 2 表达升高。SKI 治疗以剂量非依赖性方式强烈阻止这些变化。SKI 治疗可防止 HG 诱导的促衰老分子哺乳动物雷帕霉素靶蛋白和 p66Shc 的上调,以及抗衰老分子 klotho、sirt1 和过氧化物酶体增殖物激活受体-γ在肾小管上皮细胞中的下调。SKI 可能是治疗糖尿病肾病中防止 HG 诱导的肾小管细胞衰老的一种新策略。

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