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FK506 facilitates the normalization of post-ischemic perturbation of protein kinases and tyrosine phosphorylation in the gerbil hippocampal CA1 sectors

机译:FK506促进了蛋白激酶术后缺血性扰动的标准化,并在Gerbil海马CA1部门中抑制蛋白激酶和酪氨酸磷酸化

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To explore effects of immunosuppressant FK506 on signal transduction pathway, we studied changes in subcellular distribution of protein kinase C_(gamma) (PKC7), CaM kinase II (CaMKII), as well as changes of tyrosine phosphorylation levels after ischemia.Male Mongolian gerbils were divided into three groups; FK506 (1 and 3 mg/kg) and vehicle. FK506 was administered intravenously after 5 min ischemia. At the designated time points (0 time, 5 min ischemia, 1 or 24 h recovery), heads were frozen and samples were taken from CA1 subfield of hippocampus. Western blot analysis was carried out with specific antibodies for PKC7, CaMKII, and phosphotyrosine.FK506 administration significantly decreased translocation of PKC7 and CaMKII at 24 h of recovery (p < 0.05, ANOVA followed by Student Newman-Keuls' test) hi P2 fraction. The levels of tyrosine phosphorylated p160, pl40, pl00, p90, and p80 in P2 fraction were decreased with FK506 treatment at 24 h of recovery.The persistently elevated PKC7 and CaMKII level in P2 fraction, which may be related to cell death, are attenuated with FK506 treatment. FK506 may contribute to recover calcium homeostasis in post ischemic phase and promote cell survival.
机译:为了探讨免疫抑制剂FK506对信号转导途径的影响,我们研究了蛋白激酶C_(γ)(PKC7),CAM激酶II(Camkii)的亚细胞分布的变化,以及缺血后酪氨酸磷酸化水平的变化。分为三组; FK506(1和3毫克/千克)和车辆。 5分钟缺血后静脉内施用FK506。在指定的时间点(0次,5分钟缺血,1或24小时恢复),头部被冷冻,并从海马的CA1子场中取样。对于PKC7,Camkii和PhosPotorosine.fk506给药的特异性抗体进行了Western印迹分析,在24小时内显着降低了PKC7和Camkii的易位(P <0.05,Anova,然后是学生Newman-Keuls'Sear)HI P2分数。在24小时的情况下,P2级分的酪氨酸磷酸化P160,PL40,PL00,P90和P80的水平降低了24小时。P3级分的PKC7和CAMKII水平持续升高,这可能与细胞死亡有关用FK506治疗。 FK506可能有助于在缺血阶段回收钙稳态,促进细胞存活。

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