Cellular Adaptations to Neuroleptic Treatment in the Dorsal Striatum

背侧纹状体细胞对抗精神病药治疗的适应

• 批准号: 7683742
• 负责人: Tracy S Gertler
• 金额: $ 3.59万
• 依托单位: NORTHWESTERN UNIVERSITY AT CHICAGO
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-09-01 至 2010-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7683742
• 关键词: Action Potentials; Acute; Address; Affect; Animal Model; Antipsychotic Agents; Autopsy; Back; Backcrossings; Binding; Biochemical; Biological Assay; Cells; Chronic; Clinical; Clozapine; Comorbidity; Complement; Complex; Corpus striatum structure; Coupled; Delusions; Dendritic Spines; Diffuse; Disease; Disorder by Site; Dopamine; Dopamine Receptor; Dorsal; Dyes; Electrodes; Electron Microscopy; Electrophysiology (science); Event; Excitatory Synapse; Exposure to; Frequencies; Functional Magnetic Resonance Imaging; Functional disorder; G-Protein-Coupled Receptors; GTP-Binding Proteins; Gated Ion Channel; Genes; Glutamates; Guanosine Triphosphate Phosphohydrolases; Hallucinations; Haloperidol; Human Genome; Image; Impairment; Inherited; Ion Channel; Knockout Mice; Knowledge; Laser Scanning Microscopy; Life; Link; Location; Measures; Membrane; Metabolic; Modeling; Modification; Molecular; Morphology; Mus; Nature; Neurons; Neurotransmitters; Parkinsonian Disorders; Pathology; Pathway interactions; Patients; Pattern; Perception; Pharmaceutical Preparations; Photons; Physiologic pulse; Physiological; Physiology; Population; Potassium Channel; Preparation; Process; Property; Proteins; Relapse; Research Training; Residual state; Resolution; Role; Schizophrenia; Sensory; Site; Slice; Structure; Sum; Susceptibility Gene; Symptoms; Synapses; Synaptic plasticity; System; Techniques; Thalamic structure; Tissue Sample; Tissues; Transgenic Mice; Transgenic Organisms; Translations; Vertebral column; base; cell type; congenic; density; extracellular; imaging modality; improved; in vivo; insight; mouse model; neuronal cell body; neuropsychiatry; neuroregulation; neurotransmission; palliative; patch clamp; postsynaptic; presynaptic; promoter; protein expression; receptor; receptor expression; remediation; response; synaptic function; tissue slice preparation; tool; transmission process; voltage

DESCRIPTION (provided by applicant): Schizophrenia affects 1% of the population worldwide; neuroleptic (antipsychotic) medications are essential for treatment despite an incomplete understanding of the mechanisms through which palliative symptomatic remediation is exerted. Though different in the degree of antagonism for the dopamine 2 receptor (D2R) and extradopaminergic effects, both 'typical1 neuroleptics (e.g. haloperidol) and 'atypical1 neuroleptics such as clozapine are effective at long-term remodeling of the corticostriatal synapse, a primary site of disease pathophysiology and pharmacotherapeutic activity as demonstrated by in vivo imaging and postmortem tissue analyses. Previous study has been impeded by an inability to experimentally separate a heterogeneous cell population in the striatum, and by inadequate resolution from the soma of dendritic processes. BAG transgenic mice expressing eGFP under the dopamine 1 receptor (D1R) and D2R promoters will be used to distinguish dichotomous principal neuron populations in the striatum, in combination with 2-photon laser scanning microscopy (2PLSM) to gain insight into dendritic function. As adaptations to chronic neuroleptic administration may be different in normal versus diseased states, an RGS4 knockout mouse will be employed as a schizophrenic-like model in parallel to wildtype strains; RGS4 has been implicated as both a schizophrenia susceptibility gene in cases of demonstrable hereditary transmission and a gene sensitive to altered dopamine transmission in the striatum of Parkinsonian animal models. In summary, this proposal aims to characterize the compound effect by which pharmacotherapeutic improvement in clinical symptomatology is effected. Whole-cell patch clamp electrophysiology, combined with molecular transgenic, pharmacologic, and 2-photon imaging modalities will be used to study the remodeling of neuronal subpopulations in the dorsal striatum of wildtype and RGS4 knockout mice following subchronic typical (i.e. haloperidol) and atypical (i.e. clozapine) neuroleptic administration. Specific Aim 1 will examine the intrinsic, morphologic, and dendritic properties of medium spiny neurons of the dorsal striatum. To assess functional connectivity between prefrontal cortical and striatal neurons, Specific Aim 2 will target presynaptic and postsynaptic adjustments in the corticostriatal synapse.

描述（由申请人提供）：精神分裂症影响全球1%的人口；尽管对姑息性症状补救的机制了解不完全，但抗精神病药物对治疗是必不可少的。尽管对多巴胺2受体（D2R）和多巴胺能外作用的拮抗程度不同，但“典型”抗精神病药（如氟哌啶醇）和“非典型”抗精神病药（如氯氮平）对皮质纹状体突触的长期重塑都是有效的，皮质纹状体突触是疾病病理生理和药物治疗活性的主要部位，经体内成像和死后组织分析证实。由于无法通过实验分离纹状体中的异质细胞群，以及树突突起体的分辨率不足，先前的研究受到阻碍。在多巴胺1受体（D1R）和D2R启动子下表达eGFP的BAG转基因小鼠将被用于区分纹状体中两个主要神经元群体，并结合双光子激光扫描显微镜（2PLSM）来深入了解树突功能。由于正常和患病状态下对慢性抗精神病药的适应性可能不同，RGS4基因敲除小鼠将被用作与野生型小鼠平行的精神分裂症样模型；RGS4被认为是一种精神分裂症易感基因，在可证实的遗传传递的情况下，也是一种对帕金森病动物模型纹状体多巴胺传递改变敏感的基因。综上所述，本建议旨在描述影响临床症状的药物治疗改善的复合效应。全细胞膜片钳电生理学，结合分子转基因，药理学和双光子成像模式将用于研究野生型和RGS4基因敲除小鼠在亚慢性典型（如氟哌啶醇）和非典型（如氯氮平）给药后背纹状体神经元亚群的重塑。特异性目的1将研究背纹状体中棘神经元的内在、形态和树突特性。为了评估前额皮质和纹状体神经元之间的功能连通性，Specific Aim 2将针对皮质纹状体突触的突触前和突触后调节。