Chen J X, Zeng H, Chen X, Su C Y, Lai C C
Department of Pharmacology, Hunan Medical University, Changsha, 410078, P.R. China.
Pharmacol Res. 2001 Jan;43(1):63-9. doi: 10.1006/phrs.2000.0753.
In this study, we examined whether Ginkgo Biloba Extract and its terpenoid constituents protect against oxidative stress through actions on heme oxygenase (HO) gene expression and activity. HO-1 and glutathione peroxidase (GPx) gene expressions were examined by reverse transcription polymerase chain reaction (RT-PCR) analysis, HO activity and GPx enzyme activity were analysed by spectrophotometric assay. Pretreatment of H9c2 myocytes with 100-500 microgml(-1)Ginkgo Biloba Extract caused induction of HO-1 gene expression and a significant increase in HO activity; 30 microgml(-1)ginkgolide B and 30 microgml(-1)bilobalide had little effect. Treatment with Ginkgo Biloba Extract for 24 h also significantly increased GPx gene expression and GPx enzyme activity. Pretreatment with Ginkgo Biloba Extract, ginkgolide B and bilobalide protected myocytes against lysophosphatidylcholine (LPC)-induced damage. The protective effect of Ginkgo Biloba Extract against LPC-induced damage was partially suppressed by a HO inhibitor, Zinc protoporphyrin-IX (ZnPP-IX), while ZnPP-IX did not suppress the protective effect of ginkgolide B or bilobalide. Furthermore, pretreatment with hemin, biliverdin or bilirubin reduced cytotoxicity induced by LPC. These results suggest that induction of HO-1 by Ginkgo Biloba Extract but not its terpenoid constituents may play a beneficial role in oxidative stress. The mechanism of Ginkgo Biloba Extract-induced HO-1 gene expression and the increase in HO activity may be related to alteration of intracellular glutathione levels.
在本研究中,我们检测了银杏叶提取物及其萜类成分是否通过对血红素加氧酶(HO)基因表达和活性的作用来抵御氧化应激。通过逆转录聚合酶链反应(RT-PCR)分析检测HO-1和谷胱甘肽过氧化物酶(GPx)基因表达,通过分光光度法检测HO活性和GPx酶活性。用100 - 500μg/ml(-1)银杏叶提取物预处理H9c2心肌细胞可诱导HO-1基因表达并显著提高HO活性;30μg/ml(-1)银杏内酯B和30μg/ml(-1)白果内酯作用甚微。用银杏叶提取物处理24小时也显著增加了GPx基因表达和GPx酶活性。用银杏叶提取物、银杏内酯B和白果内酯预处理可保护心肌细胞免受溶血磷脂酰胆碱(LPC)诱导的损伤。HO抑制剂原卟啉锌-IX(ZnPP-IX)部分抑制了银杏叶提取物对LPC诱导损伤的保护作用,而ZnPP-IX并未抑制银杏内酯B或白果内酯的保护作用。此外,用血红素、胆绿素或胆红素预处理可降低LPC诱导的细胞毒性。这些结果表明,银杏叶提取物而非其萜类成分诱导HO-1可能在氧化应激中发挥有益作用。银杏叶提取物诱导HO-1基因表达及HO活性增加的机制可能与细胞内谷胱甘肽水平的改变有关。