Ye Chun-ling, Jin Yong-liang, Ye Kai-he, Qin Liang
Department of Pharmacology, Pharmacy College of Jinan University, Guangzhou 510632, China.
Zhong Yao Cai. 2007 Apr;30(4):424-8.
To investigate the effects of ginkgo biloba extract (EGb 761) on apoptosis induced by hydrogen peroxide (H2O2) in RIN-m beta-cells.
The apoptotic model was made by H2O2 exposed for six hours with a concentration of 500 micromol/L The cytotoxicity was measured by MTT. Hoechst 33258 fluorescent staining were used to detect the protective effect of EGb 761 on the apoptosis of RIN-m beta-cells induced by H2O2. Annexin V-PI double staining of Flow cytometry were used to detect apoptosis quantitively.
Compare to control group, after exposed to 500 micromol/L H2O2 for 6 hours, the apoptosis rate incereased and cell survival rate were decreased considerably (P < 0.01). Pretreated for 10 hours with EGb 761, the flow cytometry results showed that the apoptosis rate decreased and cell survival rate were increased considerably (P < 0.01, compared to H2O2 control group).
EGb 761 can decrease RIN-m beta-cells damage and apoptosis induced by H2O2.
研究银杏叶提取物(EGb 761)对过氧化氢(H2O2)诱导的RIN-mβ细胞凋亡的影响。
用浓度为500微摩尔/升的H2O2处理6小时建立凋亡模型。采用MTT法检测细胞毒性。用Hoechst 33258荧光染色检测EGb 761对H2O2诱导的RIN-mβ细胞凋亡的保护作用。采用流式细胞术Annexin V-PI双染色法定量检测细胞凋亡。
与对照组相比,500微摩尔/升H2O2处理6小时后,细胞凋亡率增加,细胞存活率显著降低(P<0.01)。用EGb 761预处理10小时,流式细胞术结果显示细胞凋亡率降低,细胞存活率显著增加(与H2O2对照组相比,P<0.01)。
EGb 761可减轻H2O2诱导的RIN-mβ细胞损伤和凋亡。