Gobbo O L, O'Mara S M
Department of Psychology and Trinity College Institute of Neuroscience, Trinity College, Dublin 2, Ireland.
Behav Brain Res. 2005 Apr 15;159(1):21-6. doi: 10.1016/j.bbr.2004.09.021. Epub 2004 Nov 5.
Previous studies have suggested that exercise in a running wheel can be neuroprotective, perhaps due to, among others, gene-expression changes after exercise, increases in trophic proteins and/or enhanced cardiovascular responsivity. Here we ask whether physical exercise or environmental enrichment provide protection after brain damage, especially in terms of recovery of cognitive function. To evaluate the neuroprotective effect of these conditions, we used the kainic acid (KA) model of neuronal injury. Systemically-administered KA induces excitotoxicity by overstimulation of glutamate receptors, resulting in neuronal death by necrosis and apoptosis. Our results show that exercise, but not enriched environment, prior to KA-induced brain damage, improved behavioural performance in both Morris watermaze and object exploration tasks. However, prior exercise did not decrease to control levels the hyperactivity normally seen in KA-treated animals, as measured by ambulation in the open field. Furthermore, both exercise and enriched environment did not protect against neuron loss in CA1, CA2 and CA3 areas of the hippocampus, despite a substantial increase in brain-derived neutrophic factor (BDNF) levels in dentate gyrus of the exercise and KA-treated animals.
先前的研究表明,在跑步轮中运动可能具有神经保护作用,这可能是由于运动后基因表达变化、营养蛋白增加和/或心血管反应性增强等多种因素。在此,我们探讨体育锻炼或环境丰富化在脑损伤后是否具有保护作用,特别是在认知功能恢复方面。为了评估这些条件的神经保护作用,我们使用了 kainic 酸(KA)诱导的神经元损伤模型。全身注射 KA 通过过度刺激谷氨酸受体诱导兴奋性毒性,导致神经元通过坏死和凋亡死亡。我们的结果表明,在 KA 诱导脑损伤之前进行运动,但不是环境丰富化,可改善 Morris 水迷宫和物体探索任务中的行为表现。然而,通过在旷场中的行走测量,先前的运动并没有将 KA 处理动物中通常出现的多动降低到对照水平。此外,尽管运动组和 KA 处理组动物齿状回中脑源性神经营养因子(BDNF)水平大幅增加,但运动和环境丰富化均未防止海马体 CA1、CA2 和 CA3 区域的神经元丢失。