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作 者:陈晓雷[1] 翟丽颖 王一然 杨秀丽[1] 李新新[1]
机构地区:[1]沈阳医学院法医司法鉴定所,辽宁沈阳110034 [2]丹东市公安医院 [3]法库县公安局
出 处:《沈阳医学院学报》2014年第4期202-204,共3页Journal of Shenyang Medical College
基 金:沈阳医学院科研课题(No.20131004)
摘 要:目的:观察z-DEVD-fmk(caspase-3抑制剂)对甲基苯丙胺(methamphetamine,MA)依赖大鼠海马组织caspase-3活性及其蛋白表达的影响。方法:选取健康Wistar大鼠40只,随机分为空白对照组、MA依赖组、MA+z-DEVD-fmk干预组和z-DEVD-fmk组,各10只。参考文献建立MA依赖大鼠实验动物模型,经侧脑室注射z-DEVD-fmk干预治疗,采用酶标仪法检测caspase-3活性,采用免疫组化法检测Caspase-3蛋白的表达。结果:与空白对照组比较,MA依赖组和MA+zDEVD-fmk干预组海马组织caspase-3活性明显升高(P<0.01),Caspase-3蛋白表达增多(P<0.01);与MA依赖组比较,Ma+z-DEVD-fmk干预组caspase-3活性明显降低(P<0.05),Caspase-3蛋白表达减少(P<0.05)。结论:z-DEVD-fmk能够抑制MA依赖大鼠海马组织caspase-3活性,降低Caspase-3蛋白表达,z-DEVD-fmk具有干预与保护MA致大鼠脑组织损伤作用。Objective: To observe the effect of z-DEVD-fmk (caspase-3 inhibitor) on caspase-3 activity and its protein expression in brain tissue of methamphetamine (MA) -dependent rats. Methods: A total of 40 Wistar rats were randomly divided into the blank control group, MA-dependent group, MA + z-DEVD-fmk group and z-DEVD-fmk group, each group had 10 rats. The experimental animal model of MA-dependent was established according to reference. After intracerebroventricular injection of z-DEVD-fmk intervention, microplate assay was used to determine the caspasc-3 activity. Immunohistochemistry method was used to detect the expression of Caspase-3 protein. Results: Compared with the blank control group, caspase-3 activity in brain tissue of MA-dependent group and MA + z-DEVD-fmk intervention group significantly increased, while Caspase-3 protein expression also increased ( P 〈 0. 01 ). Compared with MA-dependent group, caspase-3 activity decreased and Caspase-3 protein expression also decreased in MA + z-DEVD-fmk intervention group ( P 〈 0.05 ). Conclusions : z-DEVD-fmk can inhibit caspase-3 activity and expression of Caspase-3 protein in brain tissue of MA-dependent rats, which indicates that z-DEVD-fmk can prevent rats from brain damage induced by MA.
关 键 词:甲基苯丙胺 z-DEVD-fmk(caspase-3抑制剂) caspase-3 活性
分 类 号:R917.7[医药卫生—药物分析学]
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