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6-羟基-1-甲基吲哚-3-乙腈通过Nrf2失活对顺铂诱导的氧化肾毒性的保护作用

Protective effects of 6-hydroxy-1-methylindole-3-acetonitrile on cisplatin-induced oxidative nephrotoxicity via Nrf2 inactivation.

作者信息

Moon Ji Hee, Shin Ji-Sun, Kim Jong-Bin, Baek Nam-In, Cho Young-Wuk, Lee Yong Sup, Kay Hee Yeon, Kim Soo-dong, Lee Kyung-Tae

机构信息

Department of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul 130-701, Republic of Korea.

出版信息

Food Chem Toxicol. 2013 Dec;62:159-66. doi: 10.1016/j.fct.2013.08.039. Epub 2013 Aug 26.

Abstract

We previously demonstrated the ethanol extract of the roots of Brassica rapa protects against cisplatin-induced nephrotoxicity by attenuating oxidative stress. Here, we investigated the nephroprotective effects of 6-hydroxy-1-methylindole-3-acetonitrile (6-HMA), which was isolated from the roots of B. rapa, on cisplatin-induced toxicity in renal epithelial LLC-PK1 cells and in rats with acute renal injury. Pretreatment of LLC-PK1 cells with 6-HMA ameliorated cisplatin-induced cytotoxicity caused by oxidative stress, as was demonstrated by reductions in the levels of reactive oxygen species (ROS) and malondialdehyde (MDA) and increased levels of glutathione (GSH). In addition, 6-HMA inhibited cisplatin-induced heme oxygenase-1 (HO-1) expression, possibly due to the suppression of the nuclear translocation and binding activity of NF-E2-related factor 2 (Nrf2). Furthermore, 6-HMA administered rats showed lower levels of blood urea nitrogen (BUN), creatinine, and urinary lactate dehydrogenase (LDH) than cisplatin alone-treated rats in cisplatin-induced renal injury model. Moreover, 6-HMA inhibited the cisplatin-induced formation of MDA and GSH depletion and increased the activities of superoxide dismutase (SOD), catalase (CAT), and glutathione reductase (GR). Taken together, these findings indicate 6-HMA is a major active constituent from the roots of B. rapa to have a protective effect against cisplatin-induced nephrotoxicity by attenuating oxidative stress.

摘要

我们之前证明了芜菁根乙醇提取物可通过减轻氧化应激来保护肾脏免受顺铂诱导的肾毒性。在此,我们研究了从芜菁根中分离出的6-羟基-1-甲基吲哚-3-乙腈(6-HMA)对顺铂诱导的肾上皮LLC-PK1细胞毒性以及急性肾损伤大鼠的肾保护作用。用6-HMA预处理LLC-PK1细胞可改善顺铂诱导的由氧化应激引起的细胞毒性,这表现为活性氧(ROS)和丙二醛(MDA)水平降低以及谷胱甘肽(GSH)水平升高。此外,6-HMA抑制顺铂诱导的血红素加氧酶-1(HO-1)表达,这可能是由于抑制了核因子E2相关因子2(Nrf2)的核转位和结合活性。此外,在顺铂诱导的肾损伤模型中,给予6-HMA的大鼠血尿素氮(BUN)、肌酐和尿乳酸脱氢酶(LDH)水平低于单独给予顺铂的大鼠。此外,6-HMA抑制顺铂诱导的MDA形成和GSH消耗,并增加超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽还原酶(GR)的活性。综上所述,这些发现表明6-HMA是芜菁根中的一种主要活性成分,可通过减轻氧化应激对顺铂诱导的肾毒性具有保护作用。

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