Hwansodan通过Ras和丝裂原活化蛋白(MAP)激酶途径保护PC12细胞免受血清剥夺诱导的凋亡

Myung-Sunny Kim , Hong-Seob So , Ji-Sun Park , Kang-Min Lee , Byung-Soon Moon , Ho-Sub Lee , Tae-Young Kim , Seong-Keun Moon , Raekil Park
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引用次数: 19

摘要

在韩医学中,花琐丹是治疗老年痴呆和血管性痴呆的处方。本实验通过血清剥夺法研究了黄芍丹水提物对PC12细胞凋亡的神经保护作用。黄松丹对PC12细胞的血清剥夺具有明显的剂量依赖性。PC12细胞核染色显示焕素丹明显减弱核凝聚和碎裂,具有典型的神经元凋亡特征。黄松丹还能在血清缺失的PC12细胞中阻止DNA断裂和caspase-3样蛋白酶活化,并诱导44 kDa左右蛋白的酪氨酸磷酸化,通过Western blot鉴定其为ERK1,具有电泳凝胶迁移位移。此外,MEK抑制剂PD98059、Ras灭活剂α-羟基法尼基膦酸和甲伐他汀均可减弱环索丹对血清缺失PC12细胞的神经保护作用。这些结果表明Ras/MEK/ERK信号通路参与了环索丹对血清缺失PC12细胞的神经保护作用。
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Hwansodan protects PC12 cells against serum-deprivation-induced apoptosis via a mechanism involving Ras and mitogen-activated protein (MAP) kinase pathway

Hwansodan has been used as a prescription for senile and vascular dementia in Oriental medicine. We investigated the neuroprotective effects of Hwansodan water extract on the apoptotic death of PC12 cells by serum deprivation. Hwansodan significantly rescued PC12 cells from apoptotic death by serum deprivation in a dose-dependent manner. The nuclear staining of PC12 cells clearly showed that Hwansodan attenuated nuclear condensation and fragmentation, which represents typical neuronal apoptotic characteristics. Hwansodan also prevents DNA fragmentation and caspase-3-like protease activation in serum-deprived PC12 cells and induces the tyrosine phosphorylation of proteins around 44 kDa, which was identified as ERK1 with electrophoretic gel mobility shift by Western blot. In addition, MEK inhibitor PD98059 and Ras inactivator, α-hydroxyfarnesylphosphonic acid and mevastatin, attenuated the neuroprotective effects of Hwansodan in serum-deprived PC12 cells. These results indicate that Ras/MEK/ERK signaling pathway plays a role in neuroprotective effects of Hwansodan in serum-deprived PC12 cells.

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