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灯盏花素对氧糖剥夺诱导的PC12细胞损伤中PKCγ的影响。

Effects of scutellarin on PKCgamma in PC12 cell injury induced by oxygen and glucose deprivation.

作者信息

Xu Wei, Zha Ruo-Peng, Wang Wen-Yi, Wang Yi-Ping

机构信息

State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 201203, China.

出版信息

Acta Pharmacol Sin. 2007 Oct;28(10):1573-9. doi: 10.1111/j.1745-7254.2007.00502.x.

Abstract

AIM

To evaluate the neuroprotective effect and mechanisms of scutellarin (Scu) against PC12 cell injury after oxygen and glucose deprivation followed by reperfusion (OGD-Rep).

METHODS

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.

RESULTS

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.

CONCLUSION

Scu inhibits the increase of Ca2+ and the activation of PKCgamma, exerting protective effects against PC12 cell injury induced by OGD-Rep.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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