Xu Wei, Zha Ruo-Peng, Wang Wen-Yi, Wang Yi-Ping
State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 201203, China.
Acta Pharmacol Sin. 2007 Oct;28(10):1573-9. doi: 10.1111/j.1745-7254.2007.00502.x.
To evaluate the neuroprotective effect and mechanisms of scutellarin (Scu) against PC12 cell injury after oxygen and glucose deprivation followed by reperfusion (OGD-Rep).
Undifferentiated rat pheochromocytoma PC12 cells, exposed to oxygen and glucose deprivation followed by reperfusion (OGD-Rep), used as an in vitro model of ischemia/reperfusion. Cell survival was evaluated by diphenyltetrazolium bromide (MTT) assay and the amount of LDH release was determined using assay kits. Ca2+ was monitored using a fluorescent Ca2+-sensitive dye Fura-2 acetoxymethyl ester. Cell apoptosis was detected by a DNA ladder and by flow cytometric detection. The expression of protein kinase C (PKC)gamma was determined using both RT-PCR and Western blotting. The translocation of PKCgamma was assayed by subcellular fractionation and Western blotting.
OGD-Rep injury significantly elevated the level of LDH release, Ca2+, mRNA expression and the translocation of PKCgamma compared in the PC12 cells with those of the normal group. Scu (10-100 micromol/L) exerted a protective effect against OGD-Rep injury by reducing LDH release, Ca2+, the percent of apoptosis, and the translocation of PKCgamma.
Scu inhibits the increase of Ca2+ and the activation of PKCgamma, exerting protective effects against PC12 cell injury induced by OGD-Rep.
评估灯盏花素(Scu)对氧糖剥夺再灌注(OGD-Rep)后PC12细胞损伤的神经保护作用及其机制。
将未分化的大鼠嗜铬细胞瘤PC12细胞暴露于氧糖剥夺再灌注(OGD-Rep),用作缺血/再灌注的体外模型。通过噻唑蓝(MTT)法评估细胞存活率,并使用试剂盒测定乳酸脱氢酶(LDH)释放量。使用荧光钙敏感染料Fura-2乙酰甲酯监测细胞内钙离子浓度(Ca2+)。通过DNA ladder法和流式细胞术检测细胞凋亡。使用逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法(Western blotting)测定蛋白激酶C(PKC)γ的表达。通过亚细胞分级分离和蛋白质免疫印迹法检测PKCγ的转位。
与正常组相比,OGD-Rep损伤显著提高了PC12细胞中LDH释放水平、Ca2+、mRNA表达以及PKCγ的转位。Scu(10 - 100 μmol/L)通过降低LDH释放、Ca2+、细胞凋亡百分比和PKCγ的转位,对OGD-Rep损伤发挥保护作用。
Scu抑制Ca2+的升高和PKCγ的激活,对OGD-Rep诱导的PC12细胞损伤发挥保护作用。