Laboratory of Cellular Neurobiology, Department of Physiology and Biophysics, University of São Paulo, São Paulo, SP 05508-000, Brazil.
Neuroscience. 2013 May 1;237:118-29. doi: 10.1016/j.neuroscience.2013.01.060. Epub 2013 Feb 8.
Physical exercise is known to produce beneficial effects to the nervous system. In most cases, brain-derived neurotrophic factor (BDNF) is involved in such effects. However, little is known on the role of BDNF in exercise-related effects on Parkinson's disease (PD). The aim of this study was to investigate the effects of intermittent treadmill exercise-induced behavioral and histological/neurochemical changes in a rat model of unilateral PD induced by striatal injection of 6-hydroxydopamine (6-OHDA), and the role of BDNF in the exercise effects. Adult male Wistar rats were divided into two main groups: (1) injection of K252a (a blocker of BDNF receptors), and (2) without BDNF receptor blockade. These groups were then subdivided into four groups: control (CLT), sedentary (SED, non-exercised with induction of PD), exercised 3×/week during four weeks before and four weeks after the induction of PD (EXB+EXA), and exercised 3×/week during four weeks after the induction of PD (EXA). One month after 6-OHDA injections, the animals were subjected to rotational behavioral test induced by apomorphine and the brains were collected for immunohistochemistry and immunoblotting assays, in which we measured BDNF and tyrosine hydroxylase (TH) in the substantia nigra pars compacta (SNc) and the striatum (caudate-putamen, CPu). Our results showed a significant reduction of rotational asymmetry induced by apomorphine in the exercised parkinsonian rats. BDNF decreased in the SNc of the SED group, and exercise was able to revert that effect. Exercised groups exhibited reduced damage to the dopaminergic system, detected as a decreased drop of TH levels in SNc and CPu. On the other hand, BDNF blockade was capable of substantially reducing TH expression postlesion, implying enhanced dopaminergic cell loss. Our data revealed that physical exercise is capable of reducing the damage induced by 6-OHDA, and that BDNF receptors are involved in that effect.
体育锻炼对神经系统有有益影响。在大多数情况下,脑源性神经营养因子(BDNF)参与这种作用。然而,关于 BDNF 在运动对帕金森病(PD)的影响中的作用知之甚少。本研究的目的是研究 6-羟多巴胺(6-OHDA)单侧纹状体注射诱导的 PD 大鼠模型中,间歇性跑步机运动引起的行为和组织学/神经化学变化,以及 BDNF 在运动效应中的作用。成年雄性 Wistar 大鼠分为两组:(1)K252a 注射(BDNF 受体阻断剂),和(2)无 BDNF 受体阻断剂。这些组然后分为四组:对照组(CLT)、久坐(SED,未运动,PD 诱导)、PD 诱导前 4 周和诱导后 4 周每周运动 3 次(EXB+EXA)、PD 诱导后 4 周每周运动 3 次(EXA)。6-OHDA 注射后 1 个月,动物进行阿朴吗啡诱导的旋转行为测试,收集大脑进行免疫组织化学和免疫印迹分析,测量黑质致密部(SNc)和纹状体(尾壳核,CPu)中的 BDNF 和酪氨酸羟化酶(TH)。我们的结果显示,运动性帕金森大鼠的阿朴吗啡诱导旋转不对称性显著减少。SED 组 SNc 中的 BDNF 减少,运动能够逆转这种作用。运动组表现出多巴胺能系统损伤减轻,SNc 和 CPu 中的 TH 水平降低。另一方面,BDNF 阻断剂能够显著降低损伤后 TH 表达,表明多巴胺能细胞丢失增加。我们的数据表明,体育锻炼能够减轻 6-OHDA 诱导的损伤,BDNF 受体参与该作用。