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丹参酮 IIA 通过抑制线粒体通透性转换保护大鼠原代肝细胞免受四氯化碳毒性。

Tanshinone IIA protects rat primary hepatocytes against carbon tetrachloride toxicity via inhibiting mitochondria permeability transition.

机构信息

Department of Pharmacy, Fudan University Cancer Hospital, Shanghai, China.

出版信息

Pharm Biol. 2010 May;48(5):484-7. doi: 10.3109/13880200903179699.

Abstract

Tanshinone IIA (Tan IIA), one of the key components of Salvia milthorrhiza Bunge (Lamiaceae), is used to treat liver disease. The present study was carried out to investigate the possible mechanisms involved in the hepatoprotective effects of Tan IIA on carbon tetrachloride (CCl(4))-induced hepatocyte toxicity. In cultures treated with 1 or 2 microM CCl(4), Tan IIA (10-75 microM) significantly increased hepatocyte survival rates. However, only at a concentration of 75 microM could Tan IIA partially reverse the CCl(4) (3 microM)-induced decrease of survival rate (34 +/- 3% vs. 18 +/- 3%, n = 8, p < 0.01). In isolated mitochondria energized with succinate, Tan IIA could inhibit the large swelling effect induced by CCl(4) (1 and 2 microM). Base on these results, Tan IIA could protect rat primary cultured hepatocytes from CCl(4)-induced toxicity partially by the inhibitory effect on the opening of mitochondrial permeability transition (MPT).

摘要

丹参酮 IIA(Tan IIA)是唇形科植物丹参(Salvia milthorrhiza Bunge)的主要成分之一,用于治疗肝脏疾病。本研究旨在探讨 Tan IIA 对四氯化碳(CCl(4))诱导的肝细胞毒性的肝保护作用的可能机制。在培养物中用 1 或 2 μM 的 CCl(4)处理,Tan IIA(10-75 μM)显著增加肝细胞存活率。然而,只有在 75 μM 的浓度下,Tan IIA 才能部分逆转 CCl(4)(3 μM)诱导的存活率降低(34 +/- 3%对 18 +/- 3%,n = 8,p < 0.01)。在琥珀酸能化的分离线粒体中,Tan IIA 可以抑制 CCl(4)(1 和 2 μM)诱导的大肿胀效应。基于这些结果,Tan IIA 可以通过抑制线粒体通透性转换孔(MPT)的开放来部分保护大鼠原代培养肝细胞免受 CCl(4)诱导的毒性。

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