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葛根素对1-甲基-4-苯基吡啶离子诱导分化的SH-SY5Y细胞线粒体凋亡性死亡的保护作用

[Protective effects of puerarin against 1-methyl-4-phenylpyridinium-induced mitochondrial apoptotic death in differentiated SH-SY5Y cells].

作者信息

Cheng Yuefa, Zhu Guoqi, Guan Yali, Liu Yingshuo, Hu Yan, Li Qinglin

机构信息

Jitang College of Hebei United University, Tangshan 063000, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2011 May;36(9):1222-6.

Abstract

It is well known that puerarin possesses protective activity on neurodegenerative diseases. However, the exact path way involved in the protective effect of puerarin on MPP+ -induced cell death is unclear. In this study, we focused on mitochondria im pairment in the apoptotic process of MPP+ -elicited SH-SY5Y cells and detected the protection of puerarin. As evidenced by Trypan blue assay, the cell viability was significantly decreased by 1 mmol x L(-1) MPP+, but reversed by different concentrations puerarin pre treatment. Flow cytometer analysis revealed that MPP+ -induced SH-SY5Y cells apoptosis and arrested the cells in G2/M phase, where as puerarin pretreatment concentration dependently reversed the apoptosis ratio. In addition to the apoptosis ratio, 50.0 micromol x L(-1) puerarin pretreatment even altered the MPP+ -induced G2/M phase arrest. JC-1 assay suggested that MPP+ significantly opened MMP of the SH-SYSY cells; pretreatment with puerarin attenuated the deterioration of the MMP. Both ELISA and Western blotting showed that puerarin prevented the release of cytochrome c from the mitochondrial interior to the cystol elicited by MPP+. DNA ladder showed that typical DNA ladder was present in the MPP+ -induced SH-SY5Y cells. Additionally, MPP+ enhanced caspase-9 and caspase-3 ac tivity, respectively, while not caspase-8. However,the enhancement was concentration dependently blocked by puerarin pretreatment. Taken together, puerarin can modulate mitochondrial membrane potential and inhibit the cytochrome c releasing-caspase cascade to pre vent MPP+ -induced cell injury.

摘要

众所周知,葛根素对神经退行性疾病具有保护作用。然而,葛根素对MPP⁺诱导的细胞死亡的保护作用的确切途径尚不清楚。在本研究中,我们聚焦于MPP⁺诱导的SH-SY5Y细胞凋亡过程中的线粒体损伤,并检测了葛根素的保护作用。台盼蓝检测表明,1 mmol·L⁻¹ MPP⁺可显著降低细胞活力,但不同浓度的葛根素预处理可使其逆转。流式细胞仪分析显示,MPP⁺诱导SH-SY5Y细胞凋亡并使细胞停滞于G2/M期,而葛根素预处理可浓度依赖性地逆转凋亡率。除凋亡率外,50.0 μmol·L⁻¹葛根素预处理甚至可改变MPP⁺诱导的G2/M期停滞。JC-1检测表明,MPP⁺可显著开放SH-SYSY细胞的线粒体膜电位;葛根素预处理可减轻线粒体膜电位的恶化。ELISA和蛋白质印迹均显示,葛根素可阻止MPP⁺诱导的细胞色素c从线粒体内释放至胞质。DNA梯状条带显示,MPP⁺诱导的SH-SY5Y细胞中存在典型的DNA梯状条带。此外,MPP⁺分别增强了caspase-9和caspase-3的活性,但未增强caspase-8的活性。然而,葛根素预处理可浓度依赖性地阻断这种增强作用。综上所述,葛根素可调节线粒体膜电位并抑制细胞色素c释放-caspase级联反应,从而预防MPP⁺诱导的细胞损伤。

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