O'Callaghan Rachel M, Griffin Eadaoin W, Kelly Aine M
Department of Physiology, School of Medicine, and Trinity College Institute of Neuroscience, University of Dublin, Trinity College, Dublin 2, Ireland.
Hippocampus. 2009 Oct;19(10):1019-29. doi: 10.1002/hipo.20591.
The potential of exercise or environmental enrichment to prevent or reverse age-related cognitive decline in rats has been widely investigated. The data suggest that the efficacy of these interventions as neuroprotectants may depend upon the duration and nature of the protocols and age of onset. Investigations of the mechanisms underlying these neuroprotective strategies indicate a potential role for the neurotrophin family of proteins, including nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF). In this study, we have assessed the effects of 8 months of forced exercise, begun in middle-age, on the expression of long-term potentiation (LTP) and on spatial learning in the Morris water maze in aged Wistar rats. We also assessed these measures in a cage control group and in a group of rats exposed to the stationary treadmill for the same duration as the exercised rats. Our data confirm an age-related decline in expression of LTP and in spatial learning concomitant with decreased expression of NGF and BDNF mRNA in dentate gyrus (DG). The age-related impairments in both plasticity and growth factor expression were prevented in the long-term exercised group and, surprisingly, the treadmill control group. Given the extensive handling that the treadmill control group received and their regular exposure to an environment outside the home cage, this group can be considered to have experienced environmentally enriched conditions when compared with the cage control group. Significant correlations were observed between both learning and LTP and the expression of NGF and BDNF mRNA in the dentate gyrus. We conclude that decreased expression of NGF and BDNF in the dentate gyrus of aged rats is associated with impaired LTP and spatial learning. We suggest that the reversal of these age-related impairments by enrichment and exercise may be linked with prevention of the age-related decline in expression of these growth factors and, furthermore, that enrichment is as efficacious as exercise in preventing this age-related decline.
运动或环境富集预防或逆转大鼠年龄相关性认知衰退的潜力已得到广泛研究。数据表明,这些干预措施作为神经保护剂的功效可能取决于方案的持续时间和性质以及发病年龄。对这些神经保护策略潜在机制的研究表明,神经营养因子家族蛋白,包括神经生长因子(NGF)和脑源性神经营养因子(BDNF),可能发挥作用。在本研究中,我们评估了中年开始的8个月强迫运动对老年Wistar大鼠海马长时程增强(LTP)表达和Morris水迷宫空间学习的影响。我们还在笼养对照组和与运动大鼠运动时间相同的固定跑步机暴露组中评估了这些指标。我们的数据证实,LTP表达和空间学习能力随年龄增长而下降,同时齿状回(DG)中NGF和BDNF mRNA表达也降低。长期运动组以及令人惊讶的跑步机对照组中,可塑性和生长因子表达方面与年龄相关的损伤均得到预防。鉴于跑步机对照组受到广泛的处理且经常暴露于笼外环境,与笼养对照组相比,该组可被认为经历了环境富集条件。在学习和LTP以及齿状回中NGF和BDNF mRNA表达之间观察到显著相关性。我们得出结论,老年大鼠齿状回中NGF和BDNF表达降低与LTP受损和空间学习能力下降有关。我们认为,富集和运动对这些与年龄相关损伤的逆转可能与预防这些生长因子表达的年龄相关性下降有关,此外,富集在预防这种与年龄相关的下降方面与运动同样有效。