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芍药苷对辐射诱导的细胞损伤的保护作用涉及活性氧和丝裂原活化蛋白激酶的调节。

Protective effect of paeoniflorin on irradiation-induced cell damage involved in modulation of reactive oxygen species and the mitogen-activated protein kinases.

作者信息

Li Chun Rong, Zhou Zhe, Zhu Dan, Sun Yu Ning, Dai Jin Ming, Wang Sheng Qi

机构信息

Department of Biotechnology, Beijing Institute of Radiation Medicine, Taiping Road 27#, Beijing 100850, People's Republic of China.

出版信息

Int J Biochem Cell Biol. 2007;39(2):426-38. doi: 10.1016/j.biocel.2006.09.011. Epub 2006 Oct 12.

DOI:10.1016/j.biocel.2006.09.011
PMID:17097910
Abstract

Ionizing radiation can induce DNA damage and cell death by generating reactive oxygen species (ROS). The objective of this study was to investigate the radioprotective effect of paeoniflorin (PF, a main bioactive component in the traditional Chinese herb peony) on irradiated thymocytes and discover the possible mechanisms of protection. We found 60Co gamma-ray irradiation increased cell death and DNA fragmentation in a dose-dependent manner while increasing intracellular ROS. Pretreatment of thymocytes with PF (50-200 microg/ml) reversed this tendency and attenuated irradiation-induced ROS generation. Hydroxyl-scavenging action of PF in vitro was detected through electron spin resonance assay. Several anti-apoptotic characteristics of PF, including the ability to diminish cytosolic Ca2+ concentration, inhibit caspase-3 activation, and upregulate Bcl-2 and downregulate Bax in 4Gy-irradiated thymocytes were determined. Extracellular regulated kinase (ERK), c-Jun NH2-terminal kinase (JNK), and p38 kinase were activated by 4Gy irradiation, whereas its activations were partly blocked by pretreatment of cells with PF. The presence of ERK inhibitor PD98059, JNK inhibitor SP600125 and p38 inhibitor SB203580 decreased cell death in 4Gy-irradiated thymocytes. These results suggest PF protects thymocytes against irradiation-induced cell damage by scavenging ROS and attenuating the activation of the mitogen-activated protein kinases.

摘要

电离辐射可通过产生活性氧(ROS)诱导DNA损伤和细胞死亡。本研究的目的是探讨芍药苷(PF,一种传统中药芍药中的主要生物活性成分)对受辐照胸腺细胞的辐射防护作用,并发现可能的保护机制。我们发现60Coγ射线照射以剂量依赖的方式增加细胞死亡和DNA片段化,同时增加细胞内ROS。用PF(50 - 200μg/ml)预处理胸腺细胞可逆转这种趋势,并减弱辐射诱导的ROS生成。通过电子自旋共振分析检测了PF在体外的羟基清除作用。确定了PF的几种抗凋亡特性,包括降低4Gy辐照胸腺细胞中胞质Ca2+浓度、抑制caspase-3活化以及上调Bcl-2和下调Bax的能力。细胞外调节激酶(ERK)、c-Jun氨基末端激酶(JNK)和p38激酶被4Gy辐照激活,而细胞用PF预处理可部分阻断其激活。ERK抑制剂PD98059、JNK抑制剂SP600125和p38抑制剂SB203580的存在可降低4Gy辐照胸腺细胞中的细胞死亡。这些结果表明,PF通过清除ROS和减弱丝裂原活化蛋白激酶的激活来保护胸腺细胞免受辐射诱导的细胞损伤。

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