Suppr超能文献

植物酚二萜类化合物 carnosol 可抑制 C6 神经胶质细胞中硝普钠诱导的毒性。

The plant phenolic diterpene carnosol suppresses sodium nitroprusside-induced toxicity in c6 glial cells.

机构信息

Department of Biotechnology, Chosun University, Gwangju 501-759, Republic of Korea.

出版信息

J Agric Food Chem. 2010 Feb 10;58(3):1543-50. doi: 10.1021/jf903294x.

Abstract

Carnosol, a naturally occurring bioactive phenolic diterpene originating from rosemary and sage, has been shown to exert antioxidant and anti-inflammatory effects. This study examined possible protective effects of carnosol on sodium nitroprusside (SNP)-induced cytotoxicity in C6 glial cells. Carnosol (1-10 microM) dose-dependently attenuated SNP (100 microM)-induced cell death and NO production. SNP-induced apoptotic characteristics, including DNA fragmentation, caspase-3 activation, and c-jun N-terminal protein kinase (JNK) phosphorylation, were significantly suppressed by carnosol (10 microM). In addition, carnosol pretreatment restored the level of reduced glutathione (GSH), which was diminished by SNP treatment. Although both SNP (100 microM) and carnosol (10 microM) stimulated the HO-1 expression time-dependently, SNP caused a temporal increase in HO-1 in early time periods (3-6 h) before cell death occurred. In contrast, carnosol induced the sustained expression of HO-1 until a late time point (24 h). The addition of 1 microM zinc protoporphyrin IX (ZnPP), a specific HO inhibitor, with SNP or carnosol further reduced cell viability. Also, the addition of ZnPP inhibited the protective effect of carnosol against SNP-induced cytotoxicity in C6 cells. These results suggest that carnosol possesses abilities to inhibit SNP-mediated glial cell death through modulation of apoptotic events and induction of HO-1 expression.

摘要

没食子酸醇,一种源于迷迭香和鼠尾草的天然生物活性酚类二萜,已被证明具有抗氧化和抗炎作用。本研究探讨了没食子酸醇对硝普钠(SNP)诱导的 C6 神经胶质细胞毒性的可能保护作用。没食子酸醇(1-10 μM)呈剂量依赖性减弱 SNP(100 μM)诱导的细胞死亡和 NO 产生。SNP 诱导的凋亡特征,包括 DNA 片段化、caspase-3 激活和 c-jun N 端蛋白激酶(JNK)磷酸化,均被没食子酸醇(10 μM)显著抑制。此外,没食子酸醇预处理恢复了因 SNP 处理而降低的还原型谷胱甘肽(GSH)水平。虽然 SNP(100 μM)和没食子酸醇(10 μM)均能随时间诱导 HO-1 表达,但 SNP 在细胞死亡发生之前的早期时间(3-6 h)引起 HO-1 的时间增加。相比之下,没食子酸醇诱导 HO-1 的持续表达直至较晚的时间点(24 h)。添加 1 μM 锌原卟啉 IX(ZnPP),一种特定的 HO 抑制剂,与 SNP 或没食子酸醇一起进一步降低细胞活力。此外,ZnPP 抑制了没食子酸醇对 SNP 诱导的 C6 细胞毒性的保护作用。这些结果表明,没食子酸醇通过调节凋亡事件和诱导 HO-1 表达来抑制 SNP 介导的神经胶质细胞死亡。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验