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作 者:袁征[1] 张璐[2] 武文卿[1] 袁子彦[2] 赵善民[2] 余琛琳[2] 林丽芳[2] 汤球[2]
机构地区:[1]军事医学科学院科技部条件处,北京100036 [2]第二军医大学实验动物中心,上海200433
出 处:《实验动物与比较医学》2015年第2期92-96,共5页Laboratory Animal and Comparative Medicine
基 金:上海市科委发展基金(121409009700)
摘 要:目的探讨侧脑室注射4,4’-二异硫氰基芪-2,2’-二磺酸(DIDS)对脑缺血再灌注(CIRI)大鼠脑组织损伤的保护作用及其机制。方法采用线栓法制备大鼠大脑中动脉栓塞(MCAO)模型,侧脑室注射法给药。脑缺血2h再灌注24h后用Zea—Longa标准进行神经功能评分;红四氮唑溶液(TTC、染色法测定大鼠脑梗死面积;Westernblot法测大鼠脑组织B淋巴细胞瘤.2(B—celllymphoma-2,Bcl-2)和天冬氨酸蛋白酶.3(Caspase-3)两种蛋白的表达水平;试剂盒测定大鼠脑组织内诱导型一氧化氮合酶(iNOS)和谷胱甘肽过氧化物酶(GSH—PX)的活性。结果100gmol/LDIDS侧脑室给药能改善大脑的神经功能,减少脑缺血面积,增加Bcl-2的表达,减少Caspase-3的表达,降低iNOS的活性。结论DIDS可以通过调节凋亡相关蛋白的表达以及降低iNOS的活性对大鼠神经细胞进行保护,减轻脑缺血再灌注损伤(CIRI)造成的脑组织损伤。Objective To explore the protective effects and mechanisms of 4,4'-diisothiocyanostibibene- 2,2'-disulfonic acid (DIDS) injected by intarcerebroventricular against cerebral ischemia-reperfusion injury (CIRI) in middle cerebral artery occlusive (MCAO) rats. Methods Focal cerebral ischemia in rats was produced by 2 h occlusion of the middle cerebral artery and 24 h reperfusion. DIDS and normal saline (NS) was injected by intarcerebroventricular. The neurologic deficit scores were investigated according to Zea-Longa's Standard. The infarct areas were assessed with software Imagepro Plus 6.0 after TTC staining. The levels of Bcl-2 and Caspase-3 in central neutral system were assessed by west- ern blot. And the activities of inducible nitric oxide synthase (iNOS) as well as glutathione peroxidase (GSH-PX) were determined by specific kit. Results DIDS (100 p.mol/L) could decrease the neurologic deficit score, reduced the infarct areas of the brain in CIRI rats, enhance the expression of Bcl-2, depresse the expression of Caspase-3, and decrease the activity of iNOS. Conclusion DIDS has a protective effect on CIRI of rat and this effect is related to enhancing the expression of Bcl-2 and diminishing Caspase-3 expression, decreasing the activity of iNOS.
关 键 词:缺血再灌注损伤(CIRI) 侧脑室注射 4 4’-二异硫氰基芪-2 2’-二磺酸(DIDs) B淋巴细胞瘤(Bcl-2) 天冬氨酸蛋白酶.3(Caspase-3) 诱导型一氧化氮合酶(iNOS) 谷胱甘肽过氧化物酶(GSH—PX)
分 类 号:R743.3[医药卫生—神经病学与精神病学]
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