丹参调节顺铂致肾损伤nrf2介导的信号通路。

Q Engineering
Si-Si Cao, Miao Yan, Zhen-Yan Hou, Ying Chen, Yun-Sheng Jiang, Xin-Rong Fan, Ping-Fei Fang, Bi-Kui Zhang
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引用次数: 12

摘要

丹参是一种治疗心血管疾病的有效药物,在肾损伤中起着重要作用。本研究采用小鼠模型研究丹参对顺铂所致肾功能障碍的影响。在顺铂治疗前4天和顺铂治疗后3天给药,剂量为3 g/kg。采用单次腹腔注射顺铂20 mg/kg诱导肾毒性。顺铂中毒72 h后处死小鼠。分析血清肌酐、尿素氮等生化指标。HE染色检测肾组织病理变化。检测抗氧化酶(GSH-Px、SOD)和过氧化产物(MDA)。Western blotting检测Nrf2及其靶基因HO-1、NQO1的蛋白表达。结果表明,丹参预处理显著降低顺铂治疗小鼠血清肌酐和血尿素氮。组织病理学检查显示丹参能减轻顺铂所致肾损害。丹参还能恢复肾组织抗氧化酶(GSH-Px和SOD)活性,使MDA含量正常化。Western blot结果显示,丹参可增强顺铂暴露小鼠Nrf2及其靶基因的表达。提示丹参对顺铂所致小鼠肾损害具有保护作用,其机制可能与上调nrf2介导的信号通路有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Danshen modulates Nrf2-mediated signaling pathway in cisplatin-induced renal injury.

Danshen, an efficacious agent for cardiovascular diseases, has been found to play an essential role in kidney injury. In the present study, the effect of Danshen on cisplatin-induced renal dysfunction was investigated in a mouse model. Danshen was administered to mice at a dose of 3 g/kg 4 days before and 3 days after cisplatin treatment. A single intraperitoneal injection of 20 mg/kg cisplatin was used to induce nephrotoxicity. The mice were sacrificed 72 h after cisplatin intoxication. Biochemical parameters including serum creatinine and blood urea nitrogen were analyzed. Histopathological changes of kidney tissues were detected using HE staining. Antioxidant enzymes (GSH-Px and SOD) and peroxidative product (MDA) were detected. Protein expressions of Nrf2 and its target genes including HO-1 and NQO1 were measured by Western blotting. The results showed that pretreatment with Danshen significantly reduced serum creatinine and blood urea nitrogen in the cisplatin-treated mice. Histopathological examination showed that Danshen mitigated the renal damage induced by cisplatin. Moreover, Danshen restored the activities of antioxidant enzymes (GSH-Px and SOD) and normalized the MDA contents in renal tissues. Western blotting revealed that Danshen enhanced the expressions of Nrf2 and its target genes in cisplatin-exposed mice. It was suggested that Danshen protects against the cisplatin-induced renal impairment in the mice, which is potentially associated with the upregulation of Nrf2-mediated signaling pathway.

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CiteScore
1.08
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3-8 weeks
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