Protective effects of ginkgo biloba leaves extract on peroxide-induced oxidative stress damage in PC12 cells
Weiqiang Chen
Taiping Hu
Ying Liu
摘要:BACKGROUND: Extracts of ginkgo biloba leaves (EGB) and its metabolites have been reported to enhance brain function and nerve behavior. It has also been hypothesized that they can protect neurons from oxidative stress.OBJECTIVE: To investigate protective effects of EGB on peroxide (H2O2)-induced oxidative stress damage in PC12 cells.DESIGN: Observational contrast study.SETTING: Department of Pathophysiology, Guangdong Pharmacological College.MATERIALS: EGB was provided by Xi'an Fujie Biotechnological Development Company; 1640 culture medium, methylthiazolyl tetrazolium (MTT), trypsin and dimathyl sulfoxide (DMSO) by Sigma Company;PC 12 cell strain by Cell Center of Medical College of Zhongshan University; calf serum by Hangzhou Sijiqing Bioengineering Company; lactate dehydrogenase (LDH) kit by Nanjing Jiancheng Bioengineering Research Institute.METHODS: The experiment was carried out in Department of Cell Biology of Guangdong Pharmacological College from June to December 2005.①Cell culture: PC 12 cells were cultured in 1640 medium containing 200 g/L fetal calf serum. The cells were diluted to 1×107 L-1 and washed every two days. Those cells were used to experiment until they grew in logarithm on solid wall.②Grouping and intervention: PC 12 cells(1×108L-1) were plated in 96-well plates with the density of 200 μL/hole and divided into three groups:normal control group (routinely adding media), H2O2 group (treating with media and H2O2 for 20 hours) and EGB group (adding media, 100 μ mol/L EGB and 100 μmol/L H2O2).③MTT assay: PC12 cells (1×108L-1) were plated in 96-well plates and divided into three groups with 8 holes for each group. Under sterile condition, cells were added with 5 g/L MTT (100 μ L) and cultured for 4 hours. And then, 200 μL DMSO fluid was added and shaken for 30 minutes until blue crystal products formed were dissolved soundly.④Experimental evaluation: Absorbance (A) at 630 nm was measured and LDH activity was measured at the same time.MAIN OUTCOME MEASURES: Results of MTT assay and LDH activity.RESULTS:①Results of MTT assay: A value was lower in the H2O2 group than that in the normal control group (P<0.01), while A value was higher in the EGB group than that in the H2O2 group (P<0.01).②LDH activity: LDH activity was higher in the H2O2 group than that in the normal control group (P<0.01),while LDH activity was lower in the EGB group than that in the H2O2 group (P<0.01).CONCLUSION: EGB can inhibit H2O2-induced oxidative stress damage in PC12 cells possibly by preventing damage to the cell membrane.
机标关键词:stress damageoxidative stressMTT assayginkgo biloba leavesprotective effectsculture mediumbrain functioncell membrane
分类号:R74(神经病学与精神病学)
资助基金:广东省科技厅博士启动基金(06300709)广东医学院校科研和教改项目(43543096)
论文发表日期:2007-01-01
在线出版日期:2025-08-15(本平台首次上网日期,不代表文献的发表时间)
页数:3( 369-371 )
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中国神经再生研究(英文版)

中国神经再生研究(英文版)

CSTPCDSCI
ISSN:1673-5374
年,卷(期):2007,2(6)
所属栏目:Traditional Chinese Medicine