MacDonald Erin, Van der Lee Heidi, Pocock David, Cole Christy, Thomas Nagheme, VandenBerg Penny M, Bourtchouladze Rusiko, Kleim Jeffrey A
Department of Neuroscience, Canadian Centre for Behavioural Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.
Neurorehabil Neural Repair. 2007 Nov-Dec;21(6):486-96. doi: 10.1177/1545968307305521. Epub 2007 Sep 6.
Rehabilitation-dependent motor recovery after cerebral ischemia is associated with functional reorganization of residual cortical tissue. Recovery is thought to occur when remaining circuitry surrounding the lesion is "retrained" to assume some of the lost function. This reorganization is in turn supported by synaptic plasticity within cortical circuitry and manipulations that promote plasticity may enhance recovery. Activation of the cAMP/CREB pathway is a key step for experience-dependent neural plasticity. Here we examined the effects of the prototypical phosphodiesterase inhibitor 4 (PDE4) rolipram and a novel PDE inhibitor (HT-0712), known to enhance cAMP/CREB signaling and cognitive function, on restoration of motor skill and cortical function after focal cerebral ischemia. Adult male rats were trained on a skilled reaching task to establish a baseline level of motor performance. Intracortical microstimulation was then used to derive high-resolution maps of forelimb movement representations within the caudal forelimb area of motor cortex contralateral to the trained paw. A focal ischemic infarct was created within approximately 30% of the caudal forelimb area. The effects of administering either rolipram or the novel PDE4 inhibitor HT-0712 during rehabilitation on motor recovery and restoration of movement representations within residual motor cortex were examined. Both compounds significantly enhanced motor recovery and induced an expansion of distal movement representations that extended beyond residual motor cortex. The expansion beyond the initial residual cortex was not observed in vehicle injected controls. Furthermore, the motor recovery seen in the HT-0712 animals was dose dependent. Our results suggest that PDE4 inhibitors during motor rehabilitation facilitate behavioral recovery and cortical reorganization after ischemic insult to levels significantly greater than that observed with rehabilitation alone.
脑缺血后依赖康复的运动恢复与残余皮质组织的功能重组有关。当围绕损伤部位的剩余神经回路被“重新训练”以承担一些丧失的功能时,恢复就被认为会发生。这种重组反过来又受到皮质神经回路内突触可塑性的支持,促进可塑性的操作可能会增强恢复。环磷酸腺苷/环磷腺苷反应元件结合蛋白(cAMP/CREB)通路的激活是经验依赖性神经可塑性的关键步骤。在此,我们研究了典型的磷酸二酯酶4(PDE4)抑制剂咯利普兰和一种新型PDE抑制剂(HT-0712)对局灶性脑缺血后运动技能和皮质功能恢复的影响,已知这两种抑制剂可增强cAMP/CREB信号传导和认知功能。成年雄性大鼠接受熟练抓握任务训练以建立运动表现的基线水平。然后使用皮质内微刺激来绘制与训练爪对侧的运动皮质尾侧前肢区域内前肢运动表征的高分辨率图谱。在尾侧前肢区域约30%的范围内制造局灶性缺血性梗死。研究了在康复期间给予咯利普兰或新型PDE4抑制剂HT-0712对残余运动皮质内运动恢复和运动表征恢复的影响。两种化合物均显著增强了运动恢复,并诱导了远端运动表征的扩展,其范围超出了残余运动皮质。在注射赋形剂的对照组中未观察到超出初始残余皮质的扩展。此外,HT-0712组动物的运动恢复呈剂量依赖性。我们的结果表明,运动康复期间的PDE4抑制剂促进了缺血性损伤后的行为恢复和皮质重组,其程度显著高于单独康复时观察到的水平。