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作 者:王允[1] 马腾飞[1] 孙晓晶[1] 王毅刚[1] 秦伟[1] 谷淑玲[1]
机构地区:[1]徐州医学院药理学教研室,江苏徐州221004
出 处:《徐州医学院学报》2009年第8期497-499,共3页Acta Academiae Medicinae Xuzhou
基 金:徐州医学院科研课题(07KJ28)
摘 要:目的研究盐酸戊乙奎醚(penehyclid ine hydrochloride,PHC)对大鼠缺氧缺糖/复氧复糖海马脑片的保护作用及机制。方法采用大鼠海马脑片缺氧缺糖/复氧复糖模型;分为正常组、缺氧缺糖/复氧复糖(H/R)组、PHC2μmol/L(PHC2组)、PHC 10μmol/L(PHC10组)、PHC 50μmol/L(PHC50组)、Sco 50μmol/L(Sco50组),测量各组LDH释放率,免疫组织化学法测定各组海马CA1区Bax、Bcl-2、Caspase-3的表达。结果PHC各组LDH释放率均较H/R组下降,以PHC50组效果最好(P<0.01)。PHC50组Bcl-2阳性细胞的表达和Bcl-2/Bax比值均较H/R组升高,Bax和Caspase-3阳性细胞表达均较H/R组降低(P(0.01)。Sco50组Bcl-2阳性细胞的表达和Bcl-2/Bax比值也较H/R组升高,Bax和Caspase-3阳性细胞表达均较H/R组降低(P(0.01)。结论PHC可能通过减少LDH释放和Caspase-3、Bax的表达,增加Bcl-2的表达减轻大鼠缺氧缺糖/复氧复糖海马脑片的损伤。Objective To investigate the protective effect of penehyclidine hydrochloride (PHC) on the apoptosis of rat hippocampal slices induced by hypoxia/hypoglycemia and reoxygenation (H/R) and the underlying mechanism. Methotis Experimental model of hypoxia/hypoglycemia and reoxygenation/glucose reintroduction was established by adoption of rat hippocampal slices, which were equally divided into 6 groups: Control group, H/R group, PHC 2 μmol · L^-1 (PHC2) group, PHC 10 μmol/L ( PHC10 ) group, PHC 50 μmol/L ( PHC50 ) group and Sco 50 μmol/L ( Sco50 ) group. The LDH release rate was used to evaluate the protective effect of PHC on the apoptosis of rat hippocampal slices induced by H/R. The expression of Bax, Bcl -2 and Caspase -3 in hippocampal CA1 field of each group were respectively detected by immunohistochemical method. Results Compared with H/R group, the LDH release rate in PHC groups decreased, with PHC50 group on the top ; the expression of Bcl - 2 positive cells and the Bcl - 2/Bax ratio in PHC50 group increased ; and the expression of Bax and Cspae - 3 positive cells decreased ( P 〈 0.01 ). Compared with H/R group, the expression of Bcl - 2 positive ceils and the Bcl -2/Bax ratio in Sco50 group increased; and the expression of Bax and Cspae -3 positive cells decreased (P 〈0.01). Conclusion PHC might attenuate the H/R -induced injuries to hippocampal slices by reducing the release rate of LDH, the expression of Caspase -3 as well as Bax and increase the expression of Bcl -2.
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