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雌激素对PD模型大鼠黑质纹状体通路的保护作用及其机制探讨
  • 期刊名称:解放军药学学报 2007 23(4):252-255
  • 时间:0
  • 分类:R964[医药卫生—药理学;医药卫生—药学] Q426[生物学—神经生物学;生物学—生理学]
  • 作者机构:[1]青岛大学医学院生理教研室,山东青岛266071
  • 相关基金:国家自然科学基金资助项目,No.30570573;山东省教育厅资助项目,No.J05L01;青岛市科学技术局资助项目,No.05-10.JC-97,05-2-JC-136
  • 相关项目:植物雌激素抗帕金森病作用的分子机制研究
中文摘要:

目的研究雌激素(Estrogen)对6-羟基多巴(6-OHDA)制备的去卵巢(OVX)帕金森病(PD)模型大鼠黑质纹状体通路的保护作用及其可能机制。方法应用6-OHDA两点注射单侧损毁内侧前脑束(MFB)制备OVXPD模型大鼠,侧脑室给予17-β雌二醇(17-βestradiol,1μg/5μl),观察大鼠旋转行为、黑质酪氨酸羟化酶(TH)基因表达、黑质铁染色阳性细胞数量和纹状体内多巴胺(DA)及其代谢产物含量的变化。结果雌激素用药组可明显减少阿朴吗啡诱导的PD模型大鼠单侧旋转行为(P〈0.01)。在损毁侧黑质,雌激素用药组TH基因的表达较PD模型组明显增加(P〈0.01);纹状体DA及其代谢产物亦较PD模型组显著升高(P〈0.01)。黑质铁染色阳性细胞数量较PD模型组明显减少(P〈0.01)。结论雌激素对PD模型大鼠黑质DA能神经元有明显的保护作用,其作用机制可能与降低铁负载有关。

英文摘要:

Ahn To investigate the protective effect of estrogen on the nigrostriatal system in the rat model of Parkinson' s disease and the mechanism. Methods Wistar female rats were ovariectomized and treated with vehicle or 17-βestradiol (1μg/5μl) intracerebroventricularly after unilateral injection of 6-OHDA into the medial forebrain bundle (MFB). The changes of apomorphine-induced rotational behavior, tyrosine hydroxylase (TH) gene expression and iron contents in substantia nigra (SN), DA and its metabolite contents in striatum were detected. Results 17-β estradiol treatment could ameliorate the rat' s rotational behavior induced by apomorphine compared to the PD model rats ( P 〈 0.05). 17-βestradiol treatment could prevent the 6-OHDA-induced decrease of TH gene expression in the ipsilateral SN compared to the 6-OHDA group ( P 〈 0.01 ). The DA, DOPAC and HVA levels in the striatum of the injured side of PD rats were significantly decreased compared with the intact side ( P 〈 0.01 ). 17-β estradiol treatment could increase DA and its contents of metabolites in the injured side of striatum compared to the 6-OHDA group ( P 〈0.01 ). Using Perls' iron staining, we also found that 17-βestradiol treatment could reverse the increase of iron staining in the ipsilateral SN compared to the 6-OHDA group ( P 〈 0.01 ). Conclusion Estrogen has neuroprotective effect on the dopaminergic neurons in the 6-OHDA induced rat model of PD. The mechanism may be related to the decrease of iron overload.

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