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管花苷B对肿瘤坏死因子α诱导的神经元细胞凋亡的保护作用。

Protective effect of tubuloside B on TNFalpha-induced apoptosis in neuronal cells.

作者信息

Deng Min, Zhao Jin-Yuan, Ju Xiao-Dong, Tu Peng-Fei, Jiang Yong, Li Zheng-Bin

机构信息

Research Center of Occupational Medicine, Peking University Third Hospital, Beijing 100083, China.

出版信息

Acta Pharmacol Sin. 2004 Oct;25(10):1276-84.

Abstract

AIM

To investigate the neuroprotective effect of tubuloside B, one of the phenylethanoids isolated from the stems of Cistanche salsa, on tumor necrosis factor-alpha (TNFalpha)-induced apoptosis in SH-SY5Y neuronal cells.

METHODS

Cell viability was analyzed using MTT assay. Apoptotic cells were detected using Hoechst33342 staining, and confirmed by DNA fragmentation and flow cytometric analysis. The activity of caspase-3 was measured with special assay kit. The concentration of free intracellular calcium was determined with the probe Indo-1 by spectrometer. The level of intracellular reactive oxygen species and the potential of mitochondrial membrane were determined by laser scanning confocal microscopy (LSCM) combined with fluorescence probe H2DCFDA or JC-1 respectively.

RESULTS

SH-SY5Y cells treated with TNFalpha 100 microg/L for 36 h showed typical morphological changes of apoptosis. DNA ladder could be observed by agarose gel electrophoresis. The highest percentage of apoptotic cells accumulated to 37.5 %. Following 36 h treatment with TNFalpha, accumulation of intracellular ROS and [Ca2+]i and decrease in mitochondrial membrane potential were observed, and caspase-3 activity increased by about five-fold compared with controls. However, pretreatment with tubuloside B (1, 10, or 100 mg/L) for 2 h attenuated the TNFalpha-mediated apoptosis. The antiapoptotic action of tubuloside B was partially dependent on an anti-oxidative stress effects, maintain of mitochondria function, decrease of concentration of free intracellular calcium and inhibition of caspase-3 activity.

CONCLUSION

Tubuloside B has the neuroprotective capacity to antagonize TNFalpha-induced apoptosis in SH-SY5Y cells and may be useful in treating some neurodegenerative diseases.

摘要

目的

研究管花苷B(从管花肉苁蓉茎中分离得到的苯乙醇苷类成分之一)对肿瘤坏死因子-α(TNFα)诱导的SH-SY5Y神经细胞凋亡的神经保护作用。

方法

采用MTT法分析细胞活力。用Hoechst33342染色检测凋亡细胞,并通过DNA片段化和流式细胞术分析进行确认。用专用试剂盒测定caspase-3的活性。用Indo-1探针通过光谱仪测定细胞内游离钙的浓度。分别通过激光扫描共聚焦显微镜(LSCM)结合荧光探针H2DCFDA或JC-1测定细胞内活性氧水平和线粒体膜电位。

结果

用100μg/L TNFα处理SH-SY5Y细胞36小时后,细胞呈现典型的凋亡形态变化。琼脂糖凝胶电泳可观察到DNA梯状条带。凋亡细胞的最高比例累积至37.5%。用TNFα处理36小时后,观察到细胞内活性氧和细胞内钙离子浓度升高,线粒体膜电位降低,与对照组相比,caspase-3活性增加了约五倍。然而,用管花苷B(1、10或100mg/L)预处理2小时可减轻TNFα介导的凋亡。管花苷B的抗凋亡作用部分依赖于抗氧化应激作用、维持线粒体功能、降低细胞内游离钙浓度以及抑制caspase-3活性。

结论

管花苷B具有拮抗TNFα诱导的SH-SY5Y细胞凋亡的神经保护能力,可能对治疗某些神经退行性疾病有用。

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