Cerebellar timing dysfunction in schizophrenia

精神分裂症的小脑计时功能障碍

基本信息

批准号：
7229527
负责人：
WILLIAM P HETRICK
金额：
$ 32.81万
依托单位：
TRUSTEES OF INDIANA UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2006
资助国家：
美国
起止时间：
2006-05-05 至 2011-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7229527
关键词：
6-Cyano-7-nitroquinoxaline-2,3-dione AMPA Receptors Accounting Address Affect Affective Antipsychotic Agents Area Behavior Behavior Disorders Behavioral Blinking Brain Cell Nucleus Cells Cerebellar Diseases Cerebellar cortex structure Cerebellum Clinical Cognitive Communication impairment Computer information processing Condition Conditioned Stimulus Conscious Data Depth Discrimination Disease Dysmetria Exhibits Fingers Functional Magnetic Resonance Imaging Functional disorder Gait Glutamates Human Impaired cognition Infusion procedures Investigation Knowledge Laboratories Lead Learning Liquid substance Localized Magnetic Resonance Imaging Measures Mediating Mental disorders Methods Modality Modeling Motor Motor output Movement Nature Neurobiology Neurosciences Nuclear Oryctolagus cuniculus Outcome Output Pathway interactions Patients Personal Satisfaction Pharmaceutical Preparations Picrotoxin Play Posture Procedures Process Property Purkinje Cells Reaction Time Research Research Personnel Role Schizophrenia Score Sensory Process Source Stimulus Structure Symptoms Synapses System Testing Thalamic structure Thinking Time Translational Research Translations base conditioning human study human subject improved indexing neural model neuromechanism neuropsychological programs psychologic relating to nervous system research study response stellate cell stimulus processing theories

项目摘要

DESCRIPTION (provided by applicant): A translational research program will investigate the integrity of cerebellar-mediated timing functions in schizophrenia and identify mechanisms that may modulate synaptic properties of cerebellar timing networks. Mounting theoretical and empirical evidence indicates that schizophrenia is associated with a fundamental disturbance in the timing of neural processes and behavior. This deficit in the temporal coordination of information processing, sometimes referred to as cognitive dysmetria, may lead to poor temporal coordination of perceptual, cognitive, affective, and motor processes. Abnormalities in a cortico-cerebellar-thalamic-cortical (CCTC) brain circuit, which is responsible for fluid, temporal coordination of sequences of behavior, are a likely source of the timing anomalies in schizophrenia. The proposed research will examine the functional integrity of the cerebellar mode of this circuit. Parallel and complementary human and non-human studies will be conducted primarily using cerebellar-dependent eye-blink conditioning tasks. The overarching aims are to: (1) comprehensively characterize the nature of the eyeblink conditioning (EEC) acquisition and timing abnormalities in schizophrenia and use a rabbit model to identify cerebellar mechanisms that may be responsible for the observed deficits; (2) examine the contribution of primary sensory processes associated with stimulus modality and intensity to the observed EBC acquisition and timing abnormalities in schizophrenia and a rabbit model; (3) systematically explore the effect of stable, antipsychotic medication treatment on EBC and other cerebellar-dependent measures of timing; and (4) determine the clinical, behavioral, and structural neuroanatomical correlates of EBC deficits in schizophrenia. Taken together, the studies will determine the functional integrity of the cerebellar node of the cortico-cerebellar-thalamic-cortical circuit in schizophrenia and test models of impaired cerebellar functioning that may give rise to timing deficits in the disorder. This research will result in knowledge about neural mechanisms associated with an extraordinarily debilitating psychological disorder, schizophrenia. A better understanding of these mechanisms will advance knowledge about the pathophysiology of schizophrenia, and may lead to the identification of neurobiological targets of treatment.

描述（由申请人提供）：转化研究计划将调查精神分裂症中小脑介导的计时功能的完整性，并确定可能调节小脑计时网络突触特性的机制。越来越多的理论和经验证据表明，精神分裂症与神经过程和行为时序的根本性紊乱有关。这种信息处理的时间协调缺陷，有时被称为认知障碍，可能导致知觉、认知、情感和运动过程的时间协调不良。负责行为序列的流体、时间协调的皮质-小脑-丘脑-皮质（CCTC）大脑回路的异常可能是精神分裂症时间异常的根源。拟议的研究将检查该电路小脑模式的功能完整性。平行和互补的人类和非人类研究将主要使用小脑依赖性眨眼调节任务进行。总体目标是：（1）全面表征精神分裂症中眨眼条件反射（EEC）获得和时间异常的性质，并使用兔子模型来识别可能导致所观察到的缺陷的小脑机制； (2) 检查与刺激方式和强度相关的初级感觉过程对精神分裂症和兔子模型中观察到的 EBC 获取和计时异常的贡献； (3) 系统地探讨稳定的抗精神病药物治疗对 EBC 和其他小脑依赖性计时指标的影响； (4) 确定精神分裂症 EBC 缺陷的临床、行为和结构神经解剖学相关性。总而言之，这些研究将确定精神分裂症中皮质-小脑-丘脑-皮质回路小脑节点的功能完整性，并测试可能导致该疾病的时间缺陷的小脑功能受损模型。这项研究将带来有关与极度衰弱的心理疾病——精神分裂症相关的神经机制的知识。更好地了解这些机制将增进对精神分裂症病理生理学的了解，并可能导致神经生物学治疗靶点的确定。