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作 者:孙亚锋[1] 唐放鸣[1] 王然[1] 张光毅[1] 金国章[1]
机构地区:[1]中科院上海药物所
出 处:《徐州医学院学报》1999年第2期89-92,共4页Acta Academiae Medicinae Xuzhou
基 金:江苏省自然科学基金;江苏省教委自然科学基金
摘 要:目的研究左旋千金藤啶碱(SPD)对Ca2+/CaMPKⅡ活性的影响。方法采用大鼠海马及纹状体脑片体外缺血模型,用放射性32P-ATP掺入法测定Ca2+/CaMPKI活性。结果体外培养的纹状体和海马脑片在缺血30min后,Ca2+/CaMPKⅡ活性均明显下降,纹状体PKA活性增加,于缺血前10min加入不同浓度SPD后,二酶活性较单纯缺血均有明显改变。Objective To study the effect of stepholidine (SPD) on Ca 2+ /CaM PKⅡand PKA activities.Methods On the in vitro models of rat striatal and hippocampal slices, the Ca 2+ /CaM PKⅡand PKA activities were determined by 32 P isotope incorporation.Results After ischemia for 30min, the Ca 2+ /CaM PKⅡ activity of rat striatal and hippocampal slices decreased significantly, and the PKA activity of rat striatal slice increased. Following the use of SPD 10 min before ischemia, the enzyme activities were significantly ameliorated as compaired with that in simple ischemia.Conclusion SPD has protective effect on the activities of PKA in rat striatal slice and of Ca 2+ /CaM PKⅡin rat striatal and hippocampal slices.
分 类 号:R743.31[医药卫生—神经病学与精神病学] R364.12[医药卫生—临床医学]
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