Kesar Trisha M, Belagaje Samir R, Pergami Paola, Haut Marc W, Hobbs Gerald, Buetefisch Cathrin M
Dept. of Rehabilitation Medicine, Emory University, Atlanta, GA, USA.
Dept. of Neurology, Emory University, Atlanta, GA, USA.
Brain Res. 2017 Sep 1;1670:106-117. doi: 10.1016/j.brainres.2017.06.015. Epub 2017 Jun 17.
Primary motor cortex (M1) plasticity is involved in motor learning and stroke motor recovery, and enhanced by increasing monoaminergic transmission. Age impacts these processes but there is a paucity of systematic studies on the effects of monoaminergic drugs in older adults. Here, in ten older adults (age 61+4years, 4 males), we determine the effects of a single oral dose of carbidopa/levodopa (DOPA), d-amphetamine (AMPH), methylphenidate (MEPH) and placebo (PLAC) on M1 excitability and motor training-induced M1 plasticity. M1 plasticity is defined as training related long lasting changes in M1 excitability and kinematics of the trained movement. At peak plasma level of the drugs, subjects trained wrist extension movements for 30min. Outcome measures were motor evoked potentials (MEPs) elicited by transcranial magnetic stimulation at increasing intensity (stimulus response curve, SRC) and peak acceleration of the trained wrist extension movements. Measures were obtained before and after completion of training. The curve parameters plateau (MEPmax), inflection point, and slope were extracted from SRC. At baseline drugs had a differential effect on curve parameters, while kinematics remained unchanged. Training alone (PLAC) increased MEPmax but did not improve kinematics. Drugs affected training-related changes of the curve parameters differently, but did not enhance them or kinematics when compared to PLAC. The results demonstrate that in the older adults, MEPH, DOPA, or AMPH have differential effects on baseline M1 excitability and training-related M1 plasticity but fail to enhance them above the naïve level.
初级运动皮层(M1)可塑性参与运动学习和中风后的运动恢复,并且通过增加单胺能传递而增强。年龄会影响这些过程,但关于单胺能药物对老年人影响的系统研究却很少。在此,我们对10名老年人(年龄61±4岁,4名男性)进行研究,确定单次口服卡比多巴/左旋多巴(多巴)、右旋苯丙胺(苯丙胺)、哌甲酯(哌醋甲酯)和安慰剂对M1兴奋性以及运动训练诱导的M1可塑性的影响。M1可塑性被定义为与训练相关的M1兴奋性和训练动作运动学的持久变化。在药物血浆浓度达到峰值时,受试者进行30分钟的腕伸展运动训练。观察指标为经颅磁刺激以递增强度诱发的运动诱发电位(MEP)(刺激反应曲线,SRC)以及训练的腕伸展运动的峰值加速度。在训练前后获取测量数据。从SRC中提取曲线参数平台期(MEPmax)、拐点和斜率。在基线时,药物对曲线参数有不同影响,而运动学保持不变。仅训练(安慰剂组)可增加MEPmax,但未改善运动学。药物对与训练相关的曲线参数变化有不同影响,但与安慰剂组相比并未增强这些变化或运动学。结果表明,在老年人中,哌醋甲酯、多巴或苯丙胺对基线M1兴奋性和与训练相关的M1可塑性有不同影响,但未能将它们增强至高于未训练水平。