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作 者:吴亮[1] 田有勇[1] 周俊山[1] 张颖冬[1]
机构地区:[1]南京医科大学附属南京医院神经内科,南京,210006
出 处:《中华神经医学杂志》2014年第9期894-898,共5页Chinese Journal of Neuromedicine
基 金:国家自然科学基金(81271418);江苏省自然科学基金(BK201254)
摘 要:目的 研究坎地沙坦酯对鱼藤酮致帕金森病(PD)大鼠的影响. 方法 10周龄雄性Lewis大鼠40只按照随机数字表法分为对照组、鱼藤酮组、鱼藤酮+坎地沙坦酯组和坎地沙坦酯组,每组10只.100 g/L水合氯醛麻醉充分后,微量渗透泵包埋于各组大鼠背部皮下.鱼藤酮[2.5~3.0 mg/(kg· d)]溶于二甲基亚砜和聚乙二醇(1∶1)混合液中,埋于鱼藤酮组大鼠微量渗透泵中;余3组给予等质量的生理盐水装于微量渗透泵中;鱼藤酮+坎地沙坦酯组大鼠同时给予坎地沙坦酯(混于0.5%甲基纤维素中)每天上午8时~12时灌胃[1 mg/(kg· d)],对照组给予等体积生理盐水灌胃.行为学检测评定运动功能等损害症状;免疫组化染色检测大鼠黑质部位酪氨酸羟化酶(TH)和α-共核蛋白表达情况;Western blotting检测黑质部位α-共核蛋白表达水平. 结果 分组4周后鱼藤酮组大鼠体质量明显减轻,降至(297.3±12.2)g;黑质部位TH阳性细胞显著减少,降至(377.0±41.6)个/mm2;α-共核蛋白表达显著增加,达到0.75±0.02;鱼藤酮+坎地沙坦酯组对应的各项值分别为(337.2±26.3)g、(639.7 ±46.0)个/mm2、0.57±0.01;二者差异有统计学意义(P<0.05).Western blotting结果与之一致. 结论 坎地沙坦酯能够通过减少TH阳性细胞凋亡及α-共核蛋白沉积起到保护PD大鼠作用.Objective To investigate the effect of candesartan cilexetil on rotenone-induced Parkinson's disease (PD) in rats.Methods Forty 10-week-old male Lewis rats were chosen in our study and equally randomized into control group,rotenone group,rotenone+candesartan cilexetil group and candesartan cilexetil group (n=10); rotenone (2.5-3.0 mg/[kg· d]) was given for 4 weeks to the rats of rotenone group and rotenone+candesartan cilexetil group by subcutaneous osmotic minipumps implantation under the back; rats in the rotenone+candesartan cilexetil group and candesartan cilexetil group were orally administered candesartan cilexetil.Neurological behavioral measurements were performed to evaluate the motor features; tyrosine hydroxylase (TH) and α-synuclein immunoreactivities in the substantia nigra pars compacta (SNc) were observed.Protein level of α-synuclein was determined by Westem blotting.Results The weight of rats in the rotenone group reduced to (297.3±12.2) g,with significant difference as compared with that of the other three groups (P〈0.05); decreased TH immunoreactivity (377.0±41.6) cells/mm2) and increased α-synuclein immunoreactivity (0.75±0.02) in the SNc of rats in the rotenone group was noted,enjoying significant differences as compared with the other three groups (P〈0.05); these values in the rotenone+candesartan cilexetil group were (337.2±26.3) g,(639.7±46.0) cells/mm2 and 0.57±0.01,respectively (P〈0.05).Western blotting confirmed that rotenone up-regulated the expression ofα-synuclein in the SNc,and candesartan ceilexetil markedly attenuated the increase (P〈0.05).Conclusion Candesartan cilexetil can protect rotenone-induced PD in rats through decreasing TH-positive cell apoptosis and α-synuclein deposition.
分 类 号:R742.5[医药卫生—神经病学与精神病学]
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