Research Project
10237412
Project Summary/Abstract Because activity-dependent plasticity is ubiquitous in the CNS, brain stimulation may have long-term effects on areas to which the stimulated area connects. These effects have received little attention. Nevertheless, recent appreciation of the long-term role of cortex in shaping spinal cord pathways suggests that the long-term spinal effects of cortical stimulation are likely to be substantial. In fact, weak electrical cortical stimulation (ECS) of rat sensorimotor cortex has lasting spinal effects. Three months after ECS ends, GABA receptors in spinal motoneurons remain decreased and the H-re?ex (analog of the spinal stretch re?ex) remains increased. This proposal seeks to determine in rats how ECS produces these spinal effects and to characterize the effects on physiological, anatomical, and molecular levels. Preliminary studies support the hypothesis that the spinal effects occur because ECS excites corticospinal tract (CST) neurons that synapse on spinal GABAergic interneurons that synapse on soleus motoneurons, that this input reduces GABA metabotropic receptors and thereby modi?es motoneuron properties so as to increase the H-re?ex (and also affect other spinal circuits), and that speci?c gene activations underlie these effects. Two speci?c aims test this hypothesis. The ?rst aim is to determine how ECS parameters affect its impact on the spinal cord and to de?ne the responsible descending pathway. ECS will be given by epidural electrodes. Pathway lesions and anatomical tracers will identify the key pathway and its spinal targets. Based on initial data and other studies, the expectation is that the CST is the essential pathway and that it connects to spinal motoneurons via GABAergic interneurons. The second aim is to characterize the short-term and long-term effects of ECS on spinal neurons and circuits on physiological, anatomical, and transcriptional levels. These studies will: examine ECS impact on motoneuron properties (e.g., ?ring threshold) and on spinal re?ex pathways; explore immunohistochemically ECS impact on GABAergic and other (e.g., glutamatergic) spinal interneurons and synapses and their receptors in soleus and other spinal motoneurons; use next-generation sequencing methods (RNA-Seq) to identify ECS-induced changes in gene expression in spinal motoneurons that correlate with and are likely to account for the changes in neuronal properties, spinal circuit function, and immunohistochemical measures. In summary, this proposal uses a well-de?ned experimental model to explore the spinal effects of cortical stimulation. By characterizing the nature and mechanisms of the spinal cord plasticity produced by this stimulation, it should provide fundamental new insight into the wider effects of cortical stimulation, and also into how the cortex modi?es the spinal cord throughout life. Furthermore, the results should guide development of stimulation protocols to further explore these effects, and stimulation protocols that can induce bene?cial plasticity to enhance functional recovery after CNS trauma or disease.
