[黄芪和三七有效成分提取物联合使用对氧化损伤PC12细胞凋亡、活性氧和线粒体膜电位的影响]。

Xiao-ping Huang, Xiao-dan Liu, Chang-qing Deng
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引用次数: 12

摘要

目的:探讨黄芪甲苷IV(黄芪有效成分)与三七有效成分三七皂苷R1、三七皂苷Rb1、三七皂苷Rg1联合抗氯化钴(CoCl₂)诱导的PC12细胞氧化损伤的作用及机制。方法:用神经生长因子诱导PC12细胞转分化后,用CoCl 2刺激PC12细胞诱导损伤。将PC12细胞分为10组,分别用相应药物进行培养。培养后,采用Hocchst 33258荧光染色法检测凋亡细胞,罗丹明123荧光染色法检测线粒体膜电位(MMP)水平,双乙酸二氯荧光素荧光染色法检测PC12细胞活性氧(ROS)含量。结果:CoCl 2诱导PC12细胞凋亡,MMP明显降低,ROS过量产生。黄芪甲苷、人参皂苷Rg1、人参皂苷Rb1和三七皂苷R1对CoCl 2诱导的PC12细胞凋亡有不同程度的抑制作用,减少了ROS的过量产生,降低了MMP的水平。联合用药效果优于单用有效成分。结论:黄芪和三七活性成分均能抑制氧化损伤诱导的PC12细胞凋亡,且两组分联用可增强其抑制作用,其作用机制可能与共同拮抗ROS生成、提高MMP有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effects of the combination of active component extracts from Astragalus membranaceus and Panax notoginseng on apoptosis, reactive oxygen species and mitochondrial membrane potential of PC12 cells with oxidative injury].

Objective: To explore the effects and mechanisms of combining astragaloside IV (the effective component of Astragalus membranaceus) with notoginsenoside R1, ginsenoside Rb1 and ginsenoside Rg1 (the effective components of Panax notoginseng) against oxidative injury in PC12 cells induced by cobalt chloride (CoCl₂).

Methods: CoCl₂ was used to stimulate PC12 cells to induce injury after transdifferentiation with nerve growth factor. Then the PC12 cells were divided into 10 groups and cultured with corresponding drugs. After culture, apoptotic cells were tested by using Hocchst 33258 fluorescent staining, the level of mitochondrial membrane potential (MMP) was analyzed by rhodamine 123 fluorescent staining and the content of reactive oxygen species (ROS) in PC12 cell was measured by dichlorofluorescin diacetate fluorescent staining.

Results: CoCl₂ induced apoptosis along with the obvious decrease of MMP as well as overproduction of ROS in PC12 cells. Astragaloside IV, ginsenosides Rg1, ginsenosides Rb1 and notoginsenoside R1 had inhibition effects in different degree on PC12 cell apoptosis induced by CoCl₂, reduced the overproduction of ROS and the decrease of MMP. The effects of the combination were better than those of active component alone.

Conclusion: Active components extracted from Astragalus and Panax notoginseng can inhibit PC12 cell apoptosis induced by oxidative injury, furthermore, the effects were enhanced by combination of these components, which may be associated with jointly antagonizing the generation of ROS and raising MMP.

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