Human Motor Control Laboratory, School of Medicine, University of Tasmania Hobart, TAS, Australia ; Movement Control and Neuroplasticity Research Group, Department of Kinesiology KU Leuven, Leuven, Belgium.
Human Motor Control Laboratory, School of Medicine, University of Tasmania Hobart, TAS, Australia.
Front Aging Neurosci. 2014 Jun 6;6:115. doi: 10.3389/fnagi.2014.00115. eCollection 2014.
Despite the abundance of research reporting the neurophysiological and behavioral effects of transcranial direct current stimulation (tDCS) in healthy young adults and clinical populations, the extent of potential neuroplastic changes induced by tDCS in healthy older adults is not well understood. The present study compared the extent and time course of anodal tDCS-induced plastic changes in primary motor cortex (M1) in young and older adults. Furthermore, as it has been suggested that neuroplasticity and associated learning depends on the brain-derived neurotrophic factor (BDNF) gene polymorphisms, we also assessed the impact of BDNF polymorphism on these effects. Corticospinal excitability was examined using transcranial magnetic stimulation before and following (0, 10, 20, 30 min) anodal tDCS (30 min, 1 mA) or sham in young and older adults. While the overall extent of increases in corticospinal excitability induced by anodal tDCS did not vary reliably between young and older adults, older adults exhibited a delayed response; the largest increase in corticospinal excitability occurred 30 min following stimulation for older adults, but immediately post-stimulation for the young group. BDNF genotype did not result in significant differences in the observed excitability increases for either age group. The present study suggests that tDCS-induced plastic changes are delayed as a result of healthy aging, but that the overall efficacy of the plasticity mechanism remains unaffected.
尽管有大量研究报告了经颅直流电刺激(tDCS)对健康年轻成年人和临床人群的神经生理和行为影响,但 tDCS 在健康老年成年人中引起的潜在神经可塑性变化的程度还不是很清楚。本研究比较了年轻和老年成年人初级运动皮层(M1)中阳极 tDCS 诱导的塑性变化的程度和时程。此外,由于已经提出神经可塑性和相关学习取决于脑源性神经营养因子(BDNF)基因多态性,我们还评估了 BDNF 多态性对这些效应的影响。使用经颅磁刺激在阳极 tDCS(30 分钟,1 mA)或假刺激前后(0、10、20、30 分钟)检查皮质脊髓兴奋性,以评估年轻和老年成年人。虽然阳极 tDCS 诱导的皮质脊髓兴奋性增加的总体程度在年轻和老年成年人之间没有可靠地变化,但老年成年人表现出延迟反应;对于老年组,最大的皮质脊髓兴奋性增加发生在刺激后 30 分钟,但对于年轻组则立即发生在刺激后。BDNF 基因型对于两个年龄组的观察到的兴奋性增加没有导致显著差异。本研究表明,健康衰老导致 tDCS 诱导的可塑性变化延迟,但可塑性机制的整体效果不受影响。