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川芎嗪减轻阿霉素诱导的大鼠肾小管细胞NRK-52E凋亡损伤。

Tetramethylpyrazine attenuates adriamycin-induced apoptotic injury in rat renal tubular cells NRK-52E.

作者信息

Cheng Chung-Yi, Sue Yuh-Mou, Chen Cheng-Hsien, Hou Chun-Cheng, Chan Paul, Chu Yen-Ling, Chen Tso-Hsiao, Hsu Yung-Ho

机构信息

Department of Internal Medicine, Taipei Medical University-Wan Fang Hospital, Taipei, Taiwan, Republic of China.

出版信息

Planta Med. 2006 Aug;72(10):888-93. doi: 10.1055/s-2006-946695. Epub 2006 Aug 10.

Abstract

Tetramethylpyrazine (TMP), a compound purified from Rhizoma Ligustici, is a widely used active ingredient in Chinese herbal medicine to treat cardiovascular diseases on account of its vasodilatory actions and antiplatelet activity. Studies have shown that TMP can remove oxygen free radicals and protect rat kidney from ischemia-reperfusion injury. In addition, adriamycin-induced nephrosis in rats is commonly used in pharmacological studies of human chronic renal diseases. Apoptosis of renal tubular cells has been reported in adriamycin-treated rats. To examine the therapeutic potential of TMP on chronic progressive renal diseases, adriamycin-induced injury in rat renal tubular cells NRK-52E has been used to monitor its protective effect. In TUNEL staining, TMP showed a dose-dependent protective effect against adriamycin-induced apoptosis in NRK-52E cells. Pretreatment of the cells with 10 or 100 microM of TMP effectively decreased the reactive oxygen species (ROS) formation induced by adriamycin, as measured in fluorescent assays. TMP was found to reduce the adriamycin-stimulated activities of caspase-3, caspase-8 and caspase-9, inhibit adriamycin-induced release of cytochrome C, and elevate the expression of Bcl-x (L). TMP was also able to inhibit the death receptor signaling pathway and suppress the activation of transcription factor NF-kappaB in adriamycin-treated NRK-52E cells. Based on the results of this study, we suggest that TMP can attenuate adriamycin-induced oxidative stress and apoptotic injury in NRK-52E cells, and that it may have therapeutic potential for patients with renal diseases. TMP: tetramethylpyrazine LDH: lactate dehydrogenase ROS: reactive oxygen species DCF: 2',7'-dichlorofluorescein TNF-alpha: tumor necrosis factor-alpha TUNEL: terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end-labeling.

摘要

川芎嗪(TMP)是从川芎中提纯的一种化合物,作为一种广泛应用于治疗心血管疾病的中药活性成分,具有血管舒张作用和抗血小板活性。研究表明,TMP可清除氧自由基,保护大鼠肾脏免受缺血再灌注损伤。此外,阿霉素诱导的大鼠肾病常用于人类慢性肾病的药理研究。有报道称,阿霉素处理的大鼠肾小管细胞会发生凋亡。为了研究TMP对慢性进行性肾病的治疗潜力,本研究利用阿霉素诱导的大鼠肾小管细胞NRK - 52E损伤来监测其保护作用。在TUNEL染色中,TMP对阿霉素诱导的NRK - 52E细胞凋亡具有剂量依赖性保护作用。用10或100微摩尔/升的TMP预处理细胞,可有效降低阿霉素诱导的活性氧(ROS)生成,这在荧光检测中得到了验证。研究发现,TMP可降低阿霉素刺激的半胱天冬酶 - 3、半胱天冬酶 - 8和半胱天冬酶 - 9的活性,抑制阿霉素诱导的细胞色素C释放,并提高Bcl - x(L)的表达。TMP还能够抑制死亡受体信号通路,并抑制阿霉素处理的NRK - 52E细胞中转录因子NF - κB的激活。基于本研究结果,我们认为TMP可减轻阿霉素诱导的NRK - 52E细胞氧化应激和凋亡损伤,对肾病患者可能具有治疗潜力。TMP:川芎嗪;LDH:乳酸脱氢酶;ROS:活性氧;DCF:2',7'-二氯荧光素;TNF - α:肿瘤坏死因子 - α;TUNEL:末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸缺口末端标记法

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