Deng Min, Zhao Jin-Yuan, Ju Xiao-Dong, Tu Peng-Fei, Jiang Yong, Li Zheng-Bin
Research Center of Occupational Medicine, Peking University Third Hospital, Beijing 100083, China.
Acta Pharmacol Sin. 2004 Oct;25(10):1276-84.
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.
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.
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.
Tubuloside B has the neuroprotective capacity to antagonize TNFalpha-induced apoptosis in SH-SY5Y cells and may be useful in treating some neurodegenerative diseases.
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。
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。
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。
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。