COX2对帕金森病小鼠黑质内多巴胺能神经元的毒性作用
前列腺素内过氧化物合酶;多巴胺;帕金森病;酪氨酸单氧化酶;小鼠,,前列腺素内过氧化物合酶;多巴胺;帕金森病;酪氨酸单氧化酶;小鼠,0引言
Toxic effect of COX2 on dopaminergic neurons of substantia nigra in mice with Parkinsons diseaseSHI Liang, ZHANG YuXin, ZHANG ZuoFeng, CHEN Hao
Department of Anatomy, North China Coal Medical College, Tangshan 063000, China
【Abstract】 AIM: To study the toxic effect of cyclooxygenase2 (COX2) on dopaminergic (DA) neurons of the substantia nigra in mice of Parkinsons disease (PD). METHODS: The PD model was produced according to the Laus method. The effects of COX2 on the number of COX2 immunoreactive cells and DA neurons in the substantia nigra pars compact (SNc), and the expression levels of COX2 and tyrosine hydroxylase (TH) in ventral midbrain, including ventral tegmental area (VTA) and substantia nigra (SN), were studied with immunohistochemical analysis and Western blot. The changes of above mentioned indexes, after giving COX2 inhibitor to those PD mice, were also studied. RESULTS: Compared with those control mice, the PD mice had the typical behaviors of PD, and the number of DA neurons in SNc and the level of TH in ventral midbrain decreased by about 63% and 77%. Meanwhile, the number of the COX2positive cells in SNc and the expression level of COX2 in ventral midbrain increased markedly. The PD mice, administered additionally by COX2 inhibitor, celecoxib, had slight behavioral symptoms, and the number of DA neurons in SNc and the expression level of TH in ventral midbrain declined by only about 37% and 41%; the number of the COX2positive cells in SNc and the expression level of COX2 in ventral midbrain were obviously downregulated, compared with those simple PD mice. CONCLUSION: COX2 is toxic to DA neurons of the PD mice. ......
您现在查看是摘要页,全文长 11658 字符。