Computational Modeling of Hippocampus in Schizophrenia

精神分裂症海马的计算模型

• 批准号: 7803631
• 负责人: PETER JOHN SIEKMEIER
• 金额: $ 17.55万
• 依托单位: MCLEAN HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-08-21 至 2012-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7803631
• 关键词: AMPA Receptors; Affinity; Antipsychotic Agents; Area; Behavior; Behavioral; Binding; Biochemical; Biological; Brain; Brain region; Cell Surface Receptors; Cells; Characteristics; Clinical; Complex; Computer Simulation; Data; Databases; Disease; Dopamine; Etiology; Exhibits; Frequencies; Functional disorder; Gap Junctions; Glutamates; Goals; Hippocampus (Brain); Impairment; Interneurons; Ion Channel; Kinetics; Lead; Learning; Lesion; Link; Literature; Memory; Modeling; Molecular; N-Methyl-D-Aspartate Receptors; N-Methylaspartate; Neurobiology; Neurons; Neurotransmitters; Outcome; Outcome Measure; Outcome Study; Patients; Pattern; Performance; Pharmaceutical Preparations; Property; Research; Research Personnel; Running; Schizophrenia; Sensory Receptors; Simulate; Symptoms; Synapses; Syndrome; System; Testing; Time; atypical antipsychotic; base; density; gamma-Aminobutyric Acid; insight; neuropathology; neuropsychiatry; programs; psychologic; psychopharmacologic; receptor; receptor density; receptor function; research study; simulation; theories; tool

DESCRIPTION (provided by applicant): While researchers have learned vast amounts about brain function at a cellular and molecular level over the past several years, we still have a poor understanding of the manner in which these phenomena give rise to behavior, and the way that neurobiological dysfunction creates psychiatric symptoms. This is particularly true for schizophrenia: while a large number of research studies have implicated hippocampus in the etiology of schizophrenia, and several possible neuroanatomic and biochemical abnormalities have been identified in this region, we still do not know how these findings, alone or in combination, lead to the clinical syndrome. Computational modeling is a research tool that allows one to make links between cellular phenomena and clinical behaviors by offering insights at the level of cells or cell ensembles as to how emergent properties arise. We have developed a computer simulation of a subsection of hippocampus CA1 incorporating 452 cells. Each cell is a biologically realistic model of a neuron, featuring an extensive dendritic arborization and Na+, Ca++, K+DR, K*AHp, K+c, and K+A channels, as well as AMPA, NMDA, and GABA synapses. We will use an elaborated version of this computational model as a tool to examine particular hypothesis regarding the hippocampal neuropathology of schizophrenia. Specifically, we will "lesion" the model in a schizophrenogenic way by separately and in combination (a) altering aspects of the GABA system, (b) disrupting the glutamatergic system, and (c) increasing dopaminergic tone. We will examine two outcome measures: oscillatory activity and performance on context-dependent memory tasks; both of these have clinical correlations with schizophrenia. Finally, we will apply a number medications, including typical and atypical antipsychotics, and examine their effects on system functioning. We expect these studies to 1) offer mechanistic and system-level insights into the neuropathological basis of the illness; 2) generate hypotheses that can subsequently be tested experimentally; and 3) identify potentially effective antipsychotic medications. Also, we hope that this study can make a contribution from a methodological point of view: though it involves only one brain area performing a discrete psychological task for a particular psychiatric illness, it is an approach that potentially can be applied to other brain regions and neuropsychiatric diseases.

描述（由申请人提供）：虽然过去几年研究人员在细胞和分子水平上对大脑功能有了大量了解，但我们对这些现象引起行为的方式以及神经生物学功能障碍产生精神症状的方式仍然知之甚少。对于精神分裂症来说尤其如此：虽然大量研究表明海马体与精神分裂症的病因有关，并且已经在该区域发现了几种可能的神经解剖学和生化异常，但我们仍然不知道这些发现单独或组合如何导致临床综合征。计算模型是一种研究工具，通过在细胞或细胞群体层面提供关于突现特性如何产生的见解，可以在细胞现象和临床行为之间建立联系。我们开发了包含 452 个细胞的海马 CA1 分区的计算机模拟。每个细胞都是神经元的生物学真实模型，具有广泛的树突状树枝化和 Na+、Ca++、K+DR、K*AHp、K+c 和 K+A 通道，以及 AMPA、NMDA 和 GABA 突触。我们将使用该计算模型的详细版本作为工具来检查有关精神分裂症海马神经病理学的特定假设。具体来说，我们将通过单独或组合（a）改变GABA系统的各个方面，（b）破坏谷氨酸系统，以及（c）增加多巴胺能张力，以精神分裂症的方式“损害”模型。我们将检查两个结果指标：振荡活动和上下文相关记忆任务的表现；这两者都与精神分裂症具有临床相关性。最后，我们将应用多种药物，包括典型和非典型抗精神病药物，并检查它们对系统功能的影响。我们期望这些研究能够：1）为疾病的神经病理学基础提供机制和系统层面的见解； 2）产生随后可以通过实验进行检验的假设； 3) 确定潜在有效的抗精神病药物。此外，我们希望这项研究能够从方法论的角度做出贡献：虽然它只涉及一个大脑区域针对特定的精神疾病执行离散的心理任务，但它是一种可能适用于其他大脑区域和神经精神疾病的方法。