Departamento de Ciências Fisiológicas, CCB, Universidade Estadual de Londrina, Caixa Postal 6001, CEP: 86051-970, Londrina, PR, Brazil.
Brain Res. 2010 Mar 4;1317:277-85. doi: 10.1016/j.brainres.2009.12.066. Epub 2010 Jan 4.
Unilateral microinjection of manganese into the rat substantia nigra pars compacta (SNpc) leads to the death of nigral neurons and a decrease in dopamine (DA) within the ipsilateral striatum. L-deprenyl, an irreversible inhibitor of monoamine oxidase B, appears to protect or rescue dopaminergic nigral neurons from the toxic effects of 6-hydroxydopamine (6-OHDA) and 1-methyl-4 phenyl-1, 2, 3, 6-tetrahydropiridine (MPTP). In this study we aimed to investigate whether L-deprenyl is able to influence the manganese neurotoxic time course. L-deprenyl rescue activity was evaluated in discontinuous posology and its protective effect was evaluated in a continuous one. Apomorphine-induced rotational behavior and striatal tyrosine hydroxylase immunostaining (TH-IS) were evaluated in both conditions at 24 h, 72 h and 168 h after intranigral microinjections. Our results indicate a failure in L-deprenyl to influence the establishment and time course of rotational response to apomorphine. Strikingly, a further decrease in the tyrosine hydroxylase immunostaining, at 168 h post microinjection in L-deprenyl-treated rats was obtained. Our data revealed no correlation between an increasing rotational behavior and reduction in TH-IS.
向大鼠黑质致密部(SNpc)单侧微量注射锰会导致黑质神经元死亡和同侧纹状体中多巴胺(DA)减少。L--deprenyl 是一种不可逆的单胺氧化酶 B 抑制剂,似乎可以保护或挽救多巴胺能黑质神经元免受 6-羟多巴胺(6-OHDA)和 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)的毒性作用。在这项研究中,我们旨在研究 L- Deprenyl 是否能够影响锰神经毒性的时间过程。以不连续的剂量方案评估 L- Deprenyl 的挽救活性,并以连续的剂量方案评估其保护作用。在纹状体酪氨酸羟化酶免疫染色(TH-IS)后 24 小时、72 小时和 168 小时,在两种情况下评估了阿扑吗啡诱导的旋转行为。我们的结果表明,L- Deprenyl 不能影响旋转反应的建立和时间过程。值得注意的是,在 L- Deprenyl 治疗的大鼠中,在微注射后 168 小时,酪氨酸羟化酶免疫染色进一步减少。我们的数据显示,旋转行为的增加与 TH-IS 的减少之间没有相关性。