Department of Pharmacology, Xuanwu Hospital of Capital Medical University, Key Laboratory for Neurodegenerative Disease of Ministry of Education, 45 Changchun Street, Beijing 100053, PR China.
Neurosci Lett. 2010 Aug 2;479(3):231-5. doi: 10.1016/j.neulet.2010.05.068. Epub 2010 Jun 1.
Western blot has been used to study the time-course effect of the two most popular parkinsonian neurotoxins, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP, i.p.) and 6-hydroxydopamine (6-OHDA, intra-substantia nigra), on the expression of several regulators of G-protein signaling (RGS2, 4 and 9) in striatum in rodents. During the few days after MPTP challenge, there was a decline (as expected) in tyrosine hydroxylase expression in the mouse striatum that was accompanied by a decline in RGS9 protein; the latter was specific and did not extend to RGS2 or RGS4 which were resistant to the MPTP challenge. Much the same pattern was observed in rats after 6-OHDA challenge, again, specific to RGS9, although the effect takes a few weeks, rather than a few days, to develop. These results may be helpful for the understanding of molecular mechanism underlying Parkinson's disease (PD) and RGS9 might involve in the striatal function associated with PD.
Western blot 已被用于研究两种最流行的帕金森神经毒素,1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP,腹腔内注射)和 6-羟基多巴胺(6-OHDA,纹状体内侧),对纹状体中几种 G 蛋白信号调节剂(RGS2、4 和 9)表达的时间进程效应。在 MPTP 挑战后的几天内,小鼠纹状体中的酪氨酸羟化酶表达下降(如预期的那样),同时 RGS9 蛋白下降;后者是特异性的,并不扩展到对 MPTP 挑战有抗性的 RGS2 或 RGS4。在大鼠中,在 6-OHDA 挑战后也观察到了类似的模式,同样是特异性的 RGS9,尽管这种作用需要数周而不是数天才能发展。这些结果可能有助于理解帕金森病(PD)的分子机制,并且 RGS9 可能涉及与 PD 相关的纹状体功能。