刘长锁, 胡金凤, 陈乃宏, 张均田. 丹酚酸B和银杏叶提取物EGb 761对β-淀粉样蛋白神经毒性抑制作用的比较J. 药学学报, 2006, 41(8): 706-711.
引用本文: 刘长锁, 胡金凤, 陈乃宏, 张均田. 丹酚酸B和银杏叶提取物EGb 761对β-淀粉样蛋白神经毒性抑制作用的比较J. 药学学报, 2006, 41(8): 706-711.
LIU Chang-suo, HU Jin-feng, CHEN Nai-hong, ZHANG Jun-tian. Comparison of the inhibitory activities of salvianolic acid B and Ginkgo biloba extract EGb 761 on neurotoxicity of β-amyloid peptideJ. Acta Pharmaceutica Sinica, 2006, 41(8): 706-711.
Citation: LIU Chang-suo, HU Jin-feng, CHEN Nai-hong, ZHANG Jun-tian. Comparison of the inhibitory activities of salvianolic acid B and Ginkgo biloba extract EGb 761 on neurotoxicity of β-amyloid peptideJ. Acta Pharmaceutica Sinica, 2006, 41(8): 706-711.

丹酚酸B和银杏叶提取物EGb 761对β-淀粉样蛋白神经毒性抑制作用的比较

Comparison of the inhibitory activities of salvianolic acid B and Ginkgo biloba extract EGb 761 on neurotoxicity of β-amyloid peptide

  • 摘要: 目的比较丹酚酸B(Sal B)和银杏叶提取物EGb 761对β-淀粉样蛋白(β-AP)纤维形成及细胞毒作用的影响。方法运用硫黄素T(ThT)荧光法和电子显微镜技术分析Sal B和EGb 761对β-AP1-40聚集和纤维形成的影响;另将β-AP25-35预先老化7 d,用MTT法和流式细胞仪检测两种提取物对此老化蛋白造成的PC12细胞毒性的保护作用,用荧光法观察β-AP25-35作用后细胞内活性氧含量的变化以及两种提取物的作用。结果Sal B和EGb 761都可有效地抑制β-AP1-40纤维的形成,明显抑制老化的β-AP25-35对PC12细胞的毒性作用,降低β-AP25-35造成的细胞内活性氧含量的增加。Sal B的有效剂量远远低于EGb 761。结论Sal B对β-AP神经毒性的抑制作用强于EGb 761。

     

    Abstract: AimTo compare the effects of salvianolic acid B (Sal B) and Ginkgo biloba extract EGb 761 on β-amyloid peptide (β-AP) fibril formation and cytotoxicity to PC12 cells. MethodsThe inhibitory effects of Sal B and EGb 761 on β-AP1-40 fibril formation were determined by using fluorescence analysis with Thioflavin T (ThT) and electron microscopic image. β-AP25-35 was aged by incubating at 37 ℃ for 7 d, then the protein was incubated with PC12 cells. The protective effects of Sal B and EGb 761 against cytotoxicity induced by aged β-AP25-35 in PC12 cells were evaluated by MTT reduction assay and flow cytometric analysis. β-AP25-35-induced accumulation of intracellular reactive oxygen species (ROS) was determined by fluorescence analysis. ResultsBoth Sal B and EGb 761 inhibited the formation of amyloid fibrils, protected PC12 cells from β-AP25-35-induced cytotoxicity, and decreased ROS accumulation caused by β-AP25-35. The effective doses of Sal B were far lower than those of EGb 761. ConclusionSal B was much more efficient than EGb 761 in inhibiting β-AP aggregation and in protecting PC12 cells from β-AP-induced cytotoxicity.

     

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