Dopaminergic Modulation of Corticostriatal Plasticity

皮质纹状体可塑性的多巴胺能调节

• 批准号: 6921059
• 负责人: THOMAS Hugh MCNEILL
• 金额: $ 33.65万
• 依托单位: UNIVERSITY OF SOUTHERN CALIFORNIA
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-02-15 至 2008-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6921059
• 关键词: brain derived neurotrophic factor; brain injury; corpus striatum; dopamine; dopamine agonists; dopamine antagonists; dopamine receptor; electron microscopy; functional ability; gene expression; gene induction /repression; growth factor receptors; in situ hybridization; laboratory rat; mature animal; neural plasticity; neuronal guidance; neuroregulation; neurotransmitter metabolism; receptor expression; sensorimotor system; synaptogenesis; western blottings

DESCRIPTION (provided by applicant): The studies proposed use a multidisciplinary approach (i.e. anatomical, pharmacological, molecular and behavioral) to further our understanding of the cellular events that underlie neural plasticity in the CMS by investigating the roles that dopamine and BDNF play in the modulation of axonal sprouting and synapse replacement in the striatum. The rationale for the study is based on previous reports from our laboratory, as well as those of others, showing that: 1) axon terminals from contralateral corticostriatal neurons reinnervate denervated synaptic sites in the striatum after a unilateral cortex lesion; 2) synapse replacement involves the differential regulation of growth associated proteins and neurotrophins that are lesion-specific; and 3) depletion of striatal dopamine in combination with a unilateral cortex lesion results in an aberrant pattern of neurotrophin and growth associated protein gene expression and synapse replacement in the striatum that slows the recovery of motor function. The overarching hypotheses to be tested are: 1) that dopamine acts through specific subtypes of dopamine receptors to up-regulate candidate molecules known to participate in the regulation of neurite outgrowth and synaptogenesis after brain injury, and 2) that a key mediator in the compensatory response to a unilateral cortex lesion is the induction of BDNF in contralateral corticostriatal neurons. We will use the rat unilateral cortex lesion model and selective dopamine agonist and antagonist drug treatments to define the roles that specific subtypes of dopamine receptors play in the regulation of reactive synaptogenesis after brain injury. We will use intra-striatal infusions of the neurotrophin antagonist trkB-IgG to test the hypothesis that neurite outgrowth and synapse formation after the cortex lesion is mediated through BDNF and the trkB receptor. We will assess lesion- and treatment effect on: 1) upregulation of candidate molecules known to participate in the regulation of neurite outgrowth, synaptogenesis and cell survival after brain injury; and 2) synapse loss and replacement. Molecular and anatomical changes will be correlated with the recovery of sensorimotor function, as measured by the rotorod, forelimb-use asymmetry and forelimb placing tests. Data from our studies are fundamental for broadening our understanding of the capacity of the brain to compensate for injury, and central to the development of new treatment strategies that can translate the basic principles of neuroplasticity into effective clinical interventions.

描述（由申请人提供）：拟定的研究使用多学科方法（即解剖学、药理学、分子学和行为学），通过研究多巴胺和BDNF在纹状体轴突发芽和突触替代的调节中的作用，进一步了解CMS中神经可塑性的细胞事件。本研究的基本原理是基于我们实验室以及其他实验室的先前报告，这些报告表明：1）单侧皮质损伤后，对侧皮质纹状体神经元的轴突终末重新支配纹状体中失神经支配的突触部位; 2）突触替代涉及损伤特异性的生长相关蛋白和神经营养因子的差异调节;和3）纹状体多巴胺的耗尽与单侧皮质损伤的组合导致纹状体中神经营养因子和生长相关蛋白基因表达和突触替代的异常模式，其减慢运动功能的恢复。要测试的首要假设是：1）多巴胺通过多巴胺受体的特定亚型来上调已知参与脑损伤后神经突生长和突触发生调节的候选分子，以及2）对单侧皮质损伤的代偿反应中的关键介质是对侧皮质纹状体神经元中BDNF的诱导。我们将使用大鼠单侧皮层损伤模型和选择性多巴胺激动剂和拮抗剂药物治疗来确定多巴胺受体的特定亚型在脑损伤后反应性突触发生的调节中所起的作用。我们将使用神经营养素拮抗剂trkB-IgG的纹状体内输注来检验皮质损伤后神经突生长和突触形成是通过BDNF和trkB受体介导的这一假设。我们将评估病变和治疗对以下方面的影响：1）已知参与脑损伤后神经突生长、突触发生和细胞存活调节的候选分子的上调; 2）突触丢失和替代。分子和解剖学变化将与感觉运动功能的恢复相关，如通过旋转棒、前肢使用不对称性和前肢放置测试所测量的。我们的研究数据对于扩大我们对大脑补偿损伤能力的理解至关重要，并且对于开发新的治疗策略至关重要，这些策略可以将神经可塑性的基本原理转化为有效的临床干预措施。