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Gene Expression Analysis for Statin-induced Cytotoxicity from Rat Primary Hepatocytes.

机译:从大鼠原代肝细胞中他汀诱导的细胞毒性的基因表达分析。

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Statins are competitive inhibitors of hydroxy-3-methyl glutaryl coenzyme A (HMG-CoA) reductase and used most frequently to reduce plasma cholesterol levels and to decrease cardiovascular events. However, statins also have been reported to have undesirable side effects such as myotoxicity and hepatotoxicity associated with their intrinsic efficacy mechanisms. Clinical studies recurrently reported that statin therapy elevated the level of liver enzymes such as ALT and AST in patients suggesting possible liver toxicity due to statins. This observation has been drawn great attention since statins are the most prescribed drugs and statin-therapy was extended to a larger number of high-risk patients. Here we employed rat primary hepatocytes and microarray technique to understand underlying mechanism responsible for statin-induced liver toxicity on cell level. We isolated genes whose expressions were commonly modulated by statin treatments and examined their biological functions. It is of interest that those genes have function related to response to stress in particular immunity and defense in cells. Our study provided the basic information on cellular mechanism of statin-induced cytotoxicity and may serve for finding indicator genes of statin-induced toxicity in rat primary hepatocytes.
机译:他汀类药物是羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶的竞争性抑制剂,最常用于降低血浆胆固醇水平和减少心血管事件。然而,据报道他汀类药物还具有与其固有功效机制相关的不良副作用,例如肌毒性和肝毒性。临床研究反复报道,他汀类药物疗法可提高患者肝酶(如ALT和AST)的水平,提示他汀类药物可能引起肝脏毒性。由于他汀类药物是处方最广泛的药物,他汀类药物疗法已扩展到更多的高危患者,因此这一观察结果引起了极大的关注。在这里,我们采用大鼠原代肝细胞和微阵列技术,以了解在细胞水平上他汀类药物诱导的肝毒性的潜在机制。我们分离了表达通常受他汀类药物治疗调节的基因,并检查了它们的生物学功能。令人感兴趣的是那些基因具有与应激反应有关的功能,特别是细胞中的免疫和防御。我们的研究提供了他汀类药物诱导的细胞毒性的细胞机制的基本信息,可能有助于寻找他汀类药物诱导的大鼠原代肝细胞毒性的指示基因。

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