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作 者:周宏智[1] 张元媛[1] 成亚琴[1] 陈鑫[1] 施建生[1]
出 处:《交通医学》2013年第6期593-596,600,共5页Medical Journal of Communications
摘 要:目的:探讨依达拉奉对6-羟基多巴胺(6-hydroxydopamine,6-OHDA)诱导的帕金森病大鼠模型的神经保护作用及其作用机制。方法:将实验动物分为神经生化学和组织学两组,各组分为⑴正常对照组6只;⑵生理盐水对照组6只;⑶依达拉奉组24只,依达拉奉又分为0.3mg/kg14d组6只,1mg/kg14d组6只,3 mg/kg14d组6只及3mg/kg28d组6只4个亚组。采用6-OHDA立体定位下注入SD大鼠左侧前脑内侧束制备帕金森病模型,观察依达拉奉对帕金森病模型大鼠的行为学改变、酪氨酸羟化酶阳性细胞数和谷胱甘肽的影响。结果:依达拉奉(3mg/kg14d)呈剂量依赖性减少APO诱发的6-OHDA大鼠帕金森病模型旋转次数(P<0.01),并能改善大鼠自发行为学变化。依达拉奉(3mg/kg14d.28d)阻止了6-OHDA导致的大鼠酪氨酸羟化酶阳性细胞数量和谷胱甘肽的减少(P<0.05)。结论:依达拉奉对6-OHDA诱导的帕金森病动物模型具有神经保护作用,依达拉奉改善6-OHDA损伤早期大鼠的行为学改变,抑制多巴胺神经元的脱失。Objective:To investigate the edaravone neuroprotective effect on the 6-OHDA-induced rat model of Parkinson's disease and its mechanism. Methods: The experimental animals were divided into two groups including the neurobiochemistry group and the histolology group, each of which was divided into three subgroups: the normal control group(n=6), the normal saline (NS)group(n=6) and the edaravone group(n=24), and the edaravone group was again divided into four subgroups including the 0.3mg/Kg 14d group(n=6), the lmg/Kg 14d group(n=6), the 3mg/Kg 14d group(n=6) and the 3mg/Kg 28d group(n=6). The model of Parkinson' s disease was induced by injecting 6-OHDA into the left medial fore- brain bundle. The effects of edaravone on the behavior of the rat and the number of positive cells of tyrosine hydroxylase (TH) and glutathione (GSH)in substantia nigra were observed. Results: Edaravone (3mg/kg14d,28d) dose-dependently de- creased the rotation behaviors of rat models induced by apomorphine (P〈0.01),ameliorated the spontaneous behavior, and prevented the decrease of the number of SN TH-positive cells and GSH induced by 6-OHDA(P〈0.05). Conclusion: Edar- avone had neuroprotective effects on the 6-OHDA-induced PD animal model, improved 6-OHDA injury in early rat be- havioral change and inhibited depigmentation of DA neurons.
关 键 词:帕金森病 依达拉奉 6-羟基多巴胺 神经元 谷胱甘肽 免疫组织化学染色法 大鼠
分 类 号:R742.5[医药卫生—神经病学与精神病学]
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