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咖啡酸(CA)可保护小脑颗粒神经元(CGNs)免受神经毒素1-甲基-4-苯基吡啶鎓(MPP+)诱导的细胞凋亡。

[Caffeic acid (CA) protects cerebellar granule neurons (CGNs) from apoptosis induced by neurotoxin 1-methyl-4-phenylpyridnium (MPP+)].

作者信息

Tian Xue-Fei, Pu Xiao-Ping

机构信息

Department of Molecular and Celluar Pharmacology, Peking University School of Pharmaceutical Sciences, Beijing 100083, China.

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2004 Feb;36(1):27-30.

Abstract

OBJECTIVE

To assess the effects of caffeic acid (CA) on MPP(+)-induced cerebellar granule neurons (CGNs) apoptosis.

METHODS

CGNs were pretreated with caffeic acid at 55, 110 and 220 micromol/L for 6 h, then treated with 100 micromol/L MPP(+) for 24 h (concentration-effect relationship). In addition CGNs were pretreated with caffeic acid at 110 micromol/L for 0 h, 6 h, 12 h, and 24 h, respectively, then treated with 100 micromol/L MPP(+) for 24 h (time-response relationship). Besides, after treatment with MPP(+) for 24 h, CGNs were incubated with caffeic acid at 55, 110 and 220 micromol/L, respectively. Cell viability was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and caspase-3 activity was assayed by caspase-3 fluorometric assay kit.

RESULTS

MTT assay revealed that caffeic acid significantly inhibited cell viability decrease induced by MPP(+), and caspase-3 fluorometric assay showed that caffeic acid efficiently suppressed caspase-3 activation in CGNs induced by MPP(+).

CONCLUSION

Caffeic acid (CA) can significantly protect CGNs from apoptosis induced by MPP(+) and may provide a useful therapeutic strategy for the treatment of Parkinson's disease.

摘要

目的

评估咖啡酸(CA)对1-甲基-4-苯基吡啶离子(MPP(+))诱导的小脑颗粒神经元(CGNs)凋亡的影响。

方法

将CGNs分别用55、110和220微摩尔/升的咖啡酸预处理6小时,然后用100微摩尔/升的MPP(+)处理24小时(浓度效应关系)。此外,将CGNs分别用110微摩尔/升的咖啡酸预处理0小时、6小时、12小时和24小时,然后用100微摩尔/升的MPP(+)处理24小时(时间反应关系)。此外,在用MPP(+)处理24小时后,将CGNs分别与55、110和220微摩尔/升的咖啡酸孵育。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法测定细胞活力,并用半胱天冬酶-3荧光检测试剂盒检测半胱天冬酶-3活性。

结果

MTT法显示咖啡酸显著抑制MPP(+)诱导的细胞活力下降,半胱天冬酶-3荧光检测显示咖啡酸有效抑制MPP(+)诱导的CGNs中半胱天冬酶-3的激活。

结论

咖啡酸(CA)可显著保护CGNs免受MPP(+)诱导的凋亡,可能为帕金森病的治疗提供一种有用的治疗策略。

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