Department of Molecular and Biomedical Pharmacology, University of Kentucky College of Medicine, Lexington, Kentucky, United States of America.
PLoS One. 2011;6(10):e26812. doi: 10.1371/journal.pone.0026812. Epub 2011 Oct 25.
Healthy brain aging and cognitive function are promoted by exercise. The benefits of exercise are attributed to several mechanisms, many which highlight its neuroprotective role via actions that enhance neurogenesis, neuronal morphology and/or neurotrophin release. However, the brain is also composed of glial and vascular elements, and comparatively less is known regarding the effects of exercise on these components in the aging brain. Here, we show that aerobic exercise at mid-age decreased markers of unhealthy brain aging including astrocyte hypertrophy, a hallmark of brain aging. Middle-aged female mice were assigned to a sedentary group or provided a running wheel for six weeks. Exercise decreased hippocampal astrocyte and myelin markers of aging but increased VEGF, a marker of angiogenesis. Brain vascular casts revealed exercise-induced structural modifications associated with improved endothelial function in the periphery. Our results suggest that age-related astrocyte hypertrophy/reactivity and myelin dysregulation are aggravated by a sedentary lifestyle and accompanying reductions in vascular function. However, these effects appear reversible with exercise initiated at mid-age. As this period of the lifespan coincides with the appearance of multiple markers of brain aging, including initial signs of cognitive decline, it may represent a window of opportunity for intervention as the brain appears to still possess significant vascular plasticity. These results may also have particular implications for aging females who are more susceptible than males to certain risk factors which contribute to vascular aging.
健康的大脑衰老和认知功能是通过锻炼来促进的。锻炼的好处归因于多种机制,其中许多机制通过增强神经发生、神经元形态和/或神经营养因子释放来突出其神经保护作用。然而,大脑也由神经胶质细胞和血管成分组成,关于锻炼对衰老大脑中这些成分的影响,人们知之甚少。在这里,我们表明,中年时进行有氧运动可以减少不健康的大脑衰老的标志物,包括星形胶质细胞肥大,这是大脑衰老的一个标志。中年雌性小鼠被分为久坐组或提供跑步轮进行六周。锻炼可降低海马星形胶质细胞和髓鞘衰老标志物,但增加血管内皮生长因子(VEGF),这是血管生成的标志物。大脑血管铸型显示,运动诱导的结构改变与周围血管内皮功能的改善有关。我们的研究结果表明,与久坐生活方式相关的星形胶质细胞肥大/反应性和髓鞘失调会随着血管功能的降低而加重。然而,这些影响似乎可以通过中年开始的运动来逆转。由于这个生命阶段与多种大脑衰老标志物的出现相吻合,包括认知能力下降的最初迹象,因此它可能是一个干预的机会窗口,因为大脑似乎仍然具有显著的血管可塑性。这些结果对于女性衰老也可能具有特殊意义,女性比男性更容易受到某些导致血管衰老的风险因素的影响。