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丹参酮 IIA 抑制硝普钠诱导的神经细胞凋亡。

Cryptotanshinone from Salviae miltiorrhizae radix inhibits sodium-nitroprusside-induced apoptosis in neuro-2a cells.

机构信息

Oriental Medicine R&D Center, College of Oriental Medicine, Dongguk University, Gyeongju 780-714, Republic of Korea.

出版信息

Phytother Res. 2012 Aug;26(8):1211-9. doi: 10.1002/ptr.3705. Epub 2012 Jan 6.

DOI:10.1002/ptr.3705
PMID:22228596
Abstract

The root of Salvia miltiorrhiza (Salviae miltiorrhizae radix), a herbal medicine has widely been used for the treatment of pain, miscarriage and oedema. In this study, we evaluated the neuroprotective effect of cryptotanshinone (CRT) from Salviae miltiorrhizae radix on sodium-nitroprusside (SNP)-induced apoptosis in neuro-2a (N2a) cells, and further investigated its action mechanism in signalling pathways. The effects of CRT against SNP-induced toxicity, mitochondrial membrane potential (MMP) changes, and oxidants/antioxidant defences and apoptotic signalling pathways were investigated in N2a cells. Cryptotanshinone significantly inhibited SNP-induced cell toxicity and the generation of reactive oxygen and nitrogen species (RONS), and improved MMP in N2a cells. Cryptotanshinone significantly suppressed SNP-induced peroxidation of lipid and protein, and the expression of Gclc mRNA. In the signalling pathway, CRT effectively blocked SNP-induced activation of NF-κB and ERK1/2 and JNK MAPK pathways through the elevation of Akt and cyclic AMP response element binding protein. Furthermore, CRT remarkably reduced the increase of mitochondrial Bax/Bcl-2 ratio, the release of cytochrome c from mitochondria to cytosol, and the activations of cytosolic procaspase-3 and nuclear inactive poly ADP (adenosine diphosphate)-ribose polymerase by SNP-induced apoptosis. These results indicate that CRT has neuroprotective effects against SNP-induced apoptosis in neuronal cells via the regulation of mitochondrial apoptotic cascades and antiapoptotic cellular signalling pathways.

摘要

丹参的根(丹参根),一种草药,已广泛用于治疗疼痛、流产和水肿。在这项研究中,我们评估了丹参酮(CRT)对神经-2a(N2a)细胞中亚硝基亚铁氰化钠(SNP)诱导的细胞凋亡的神经保护作用,并进一步研究了其在信号通路中的作用机制。研究了 CRT 对 SNP 诱导的毒性、线粒体膜电位(MMP)变化、氧化剂/抗氧化防御和凋亡信号通路的影响。丹参酮可显著抑制 SNP 诱导的 N2a 细胞毒性和活性氧和氮物种(RONS)的产生,并改善 MMP。丹参酮可显著抑制 SNP 诱导的脂质和蛋白质过氧化以及 Gclc mRNA 的表达。在信号通路中,CRT 通过提高 Akt 和环 AMP 反应元件结合蛋白,有效阻断 SNP 诱导的 NF-κB 和 ERK1/2 和 JNK MAPK 通路的激活。此外,CRT 还显著降低了 SNP 诱导的线粒体 Bax/Bcl-2 比值增加、细胞色素 c 从线粒体向细胞质释放以及细胞质中前胱天蛋白酶-3和核非活性多 ADP(腺苷二磷酸)-核糖聚合酶的激活。这些结果表明,CRT 通过调节线粒体凋亡级联和抗凋亡细胞信号通路对 SNP 诱导的神经元细胞凋亡具有神经保护作用。

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