Serotonergic Regulation of Behavioral Disinhibition

行为去抑制的血清素调节

基本信息

批准号：
6771041
负责人：
STEPHEN J BONASERA
金额：
$ 13.36万
依托单位：
UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
依托单位国家：
美国
项目类别：
财政年份：
2003
资助国家：
美国
起止时间：
2003-07-01 至 2008-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/6771041
关键词：
GABA aminotransferase behavior behavioral /social science research tag dopamine high performance liquid chromatography immunocytochemistry in situ hybridization laboratory mouse limbic system neural transmission neurons neuropsychology neuroregulation polymerase chain reaction postdoctoral investigator serotonin serotonin receptor synapses

项目摘要

DESCRIPTION (provided by applicant): Disinhibited behaviors (such as inattention, agitation, and poor socialization) are a significant problem that often accompanies mid- to late-stage dementia. These behaviors are likely caused in part by dysfunction of brain serotonin systems. This research plan addresses the role of serotonin 2C receptors (5-HT2CRs) in the control of behavioral inhibition. The research plan also provides a framework to guide the applicant's transition from senior fellow in geriatric medicine to an independent investigator who will make high quality contributions to the field of behavioral neuroscience. The studies proposed herein will test the primary hypothesis that 5-HT2C receptors regulate behavioral inhibition both by enhancing dopaminergic neurotransmission and diminishing GABA-ergic neurotransmission in the mesolimbic system. The specific aims of this project will test this hypothesis by demonstrating in wildtype and "knockout" mice lacking the 5-HT2C receptor that 1) 5-HT2CRs contribute to serotonergic influence on behavioral inhibition through regulation of mesolimbic dopamine activity, and 2) 5-HT2CRs contribute to serotonergic influence on behavioral inhibition through the regulation of GABA-ergic neurotransmission. Mice with targeted deletion of specific neurotransmitter receptors are ideal models to determine individual receptor contributions toward behavioral inhibition; furthermore, this data can be applied to the study of behavioral disturbances in aged subjects. Experimental design and methods to test these hypotheses are grounded in whole animal studies of behavior (including tests of exploration, sensorimotor gating, social interaction, locomotor coordination, locomotor activity, and anxiety-related behaviors). Neurochemical (microdialysis) and neuroanatomical studies (including in situ mRNA hybridization, and receptor immunocytochemistry) will be utilized to evaluate potential mechanisms underlying behaviors observed in wildtype and 5-HT2CR mutant mice. The applicant will take advantage of the many strengths unique to UCSF, including a highly reknowned faculty in both the basic sciences of Neuroscience and Genetics, and the clinical sciences of Medicine, Neurology, and Geriatrics. Data from this study will answer key questions regarding the mechanism of serotonin influences on control of behavioral inhibition, and will provide the groundwork to identify specific pharmacological interventions that may be successful in treating this refractory problem.

描述（由申请人提供）：行为失控（例如注意力不集中、烦躁和社交能力差）是中晚期痴呆症经常伴随的一个重大问题。这些行为可能部分是由大脑血清素系统功能障碍引起的。该研究计划探讨血清素 2C 受体 (5-HT2CR) 在控制行为抑制中的作用。该研究计划还提供了一个框架，指导申请人从老年医学高级研究员过渡到将为行为神经科学领域做出高质量贡献的独立研究者。本文提出的研究将检验主要假设，即 5-HT2C 受体通过增强中脑边缘系统中的多巴胺能神经传递和减少 GABA 能神经传递来调节行为抑制。该项目的具体目标将通过在缺乏 5-HT2C 受体的野生型和“基因敲除”小鼠中证明 1) 5-HT2CR 通过调节中脑边缘多巴胺活性对行为抑制产生血清素能影响来检验这一假设，2) 5- HT2CR 通过调节 GABA 能神经传递，对行为抑制产生血清素能影响。靶向删除特定神经递质受体的小鼠是确定个体受体对行为抑制作用的理想模型；此外，该数据还可应用于老年受试者行为障碍的研究。测试这些假设的实验设计和方法基于整体动物行为研究（包括探索、感觉运动门控、社交互动、运动协调、运动活动和焦虑相关行为的测试）。神经化学（微透析）和神经解剖学研究（包括原位 mRNA 杂交和受体免疫细胞化学）将用于评估在野生型和 5-HT2CR 突变小鼠中观察到的潜在行为机制。申请人将利用加州大学旧金山分校独特的许多优势，包括在神经科学和遗传学基础科学以及医学、神经病学和老年病学临床科学领域享有盛誉的教师队伍。这项研究的数据将回答有关血清素影响行为抑制控制机制的关键问题，并将为确定可能成功治疗这一难治性问题的特定药物干预措施奠定基础。