NEUROANATOMICAL/FUNCTIONAL CORRELATES IN FASD MODEL

FASD 模型中的神经解剖学/功能相关性

• 批准号: 8363188
• 负责人: Scott Parnell
• 金额: $ 1.23万
• 依托单位: DUKE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-07-01 至 2012-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8363188
• 关键词: Acute; Address; Adolescent; Adult; Behavioral; Brain; Cognitive; Collaborations; Data; Defect; Diagnosis; Diffusion Magnetic Resonance Imaging; Disease model; Dysmorphology; Environment; Ethanol; Fertilization; Fetal Alcohol Exposure; Fetal Alcohol Spectrum Disorder; Fetal Alcohol Syndrome; Fiber; Funding; Grant; Human; Imaging Techniques; Imaging technology; Individual; Knowledge; Long-Term Effects; Magnetic Resonance Imaging; Mentorship; Methods; Microscopy; Modeling; Motor; Mus; National Center for Research Resources; Neural Pathways; North Carolina; Pattern; Phenotype; Prevention; Principal Investigator; Research; Research Infrastructure; Resolution; Resources; Sensory; Source; Staging; Structure; Testing; Training; United States National Institutes of Health; Universities; Work; alcohol exposure; behavior test; brain tract; cost; design; experience; fetal; postnatal; research study

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. Among the most common, yet devastating, effects of prenatal ethanol exposure are those that involve the developing brain. While both structural and functional abnormalities of the brain have been described in individuals with Fetal Alcohol Syndrome (FAS)/Fetal Alcohol Spectrum Disorders (FASD), gaps remain in our understanding of the full range of these defects and of expected structural/functional correlates. Following up on the previous work of others, as well as the applicant's recent research, the experiments proposed herein are designed to examine the long-term effects of early gestational exposure on both brain structure and function and to provide correlative data. Overall, the proposed work will test the hypothesis that ethanol exposure at early gestational stages (gestational day [GD] 8 in mice; equivalent to the fourth week post fertilization in humans) results in a correlative pattern of brain dysmorphology and neurofunctional deficits that persists into adulthood. The proposed work will employ a mouse FASD model, state of the art high-resolution Magnetic Resonance Imaging (MRI), Diffusion Tensor Imaging (DTI), and a battery of cognitive, sensory, motor and other behavioral tests. In addition to furthering the applicant's training in MRI/DTI techniques, analyses and interpretation, the experiments and educational opportunities outlined in this proposal will greatly enhance the candidate's knowledge and understanding of methods designed to characterize neurofunctional phenotypes. Promise for the successful completion of this work is provided by the exceptional research environment of the University of North Carolina  Chapel Hill and of Duke University, mentorship by and collaboration with experts in the FASD field (Dr. K Sulik), behavioral analyses (Dr. S Moy), and imaging technologies (Drs A Johnson and M Styner), as well as the applicant's previous FASD research experience. Having illustrated the utility of high resolution MRI for discovery of ethanol-induced brain dysmorphology in fetal mice (Parnell et al, 2009), the proposed work will extend these analyses into postnatal stages. This work will be conducted by addressing 3 sub-hypotheses and the associated specific aims as follows: SPECIFIC AIM #1 will test the hypothesis that acute ethanol exposure on GD 8 will produce long-term morphological effects on specific regions of the mouse brain. The experiments for this aim will utilize high-resolution MRI and will entail analyses of the brains of postnatal day (PD) 12, 30, and 90 mice. SPECIFIC AIM #2 will test the hypothesis that this same ethanol exposure paradigm will alter the interconnecting neural pathways of the brain. Fiber tracts of the brains of PD 12, 30, and 90 mice will be assessed utilizing DTI. SPECIFIC AIM #3 will test the hypothesis that acute GD 8 ethanol exposure will result in neurofunctional abnormalities in adolescent and adult mice that are consistent with the observed dysmorphology. The results of these studies will provide important data regarding the long-term consequences of early gestational ethanol exposure and will, undoubtedly, promise to inform FASD diagnosis and prevention efforts.

这个子项目是许多利用资源的研究子项目之一 由NIH/NCRR资助的中心拨款提供。子项目的主要支持 而子项目的主要调查员可能是由其他来源提供的， 包括其它NIH来源。 列出的子项目总成本可能 代表子项目使用的中心基础设施的估计数量， 而不是由NCRR赠款提供给子项目或子项目工作人员的直接资金。 产前接触乙醇最常见但最具破坏性的影响是涉及发育中的大脑。虽然在患有胎儿酒精综合征（FAS）/胎儿酒精谱系障碍（FASD）的个体中描述了大脑的结构和功能异常，但我们对这些缺陷的全部范围以及预期的结构/功能相关性的理解仍然存在差距。在其他人之前的工作以及申请人最近的研究的基础上，本文提出的实验旨在检查早期妊娠暴露对大脑结构和功能的长期影响，并提供相关数据。总的来说，拟议的工作将测试这一假设，即妊娠早期（小鼠妊娠第8天[GD];相当于人类受精后第4周）的乙醇暴露导致持续到成年期的脑畸形和神经功能缺陷的相关模式。拟议的工作将采用小鼠FASD模型、最先进的高分辨率磁共振成像（MRI）、扩散张量成像（DTI）以及一系列认知、感觉、运动和其他行为测试。除了促进申请人在MRI/DTI技术，分析和解释方面的培训外，本提案中概述的实验和教育机会将大大提高候选人对旨在表征神经功能表型的方法的知识和理解。北卡罗来纳州大学的特殊研究环境为这项工作的成功完成提供了保证  查佩尔山和杜克大学，导师和合作的专家在FASD领域（博士K Sulik），行为分析（博士S Moy），和成像技术（博士A约翰逊和M Styner），以及申请人以前的FASD研究经验。已经说明了高分辨率MRI在发现乙醇诱导的胎鼠脑畸形中的实用性（帕内尔et al，2009），拟议的工作将这些分析扩展到出生后阶段。本工作将通过解决3个子假设和相关特定目标进行，具体如下：特定目标#1将检验GD 8急性乙醇暴露将对小鼠大脑特定区域产生长期形态学影响的假设。为此目的的实验将利用高分辨率MRI，并将需要对出生后12天、30天和90天的小鼠的大脑进行分析。具体目标#2将检验这一假设，即相同的乙醇暴露范例将改变大脑的互连神经通路。将使用DTI评估PD 12、30和90小鼠的脑纤维束。具体目标#3将检验以下假设：急性GD 8乙醇暴露将导致青春期和成年小鼠的神经功能异常，这与观察到的畸形一致。这些研究的结果将提供关于早期妊娠乙醇暴露的长期后果的重要数据，无疑将为FASD的诊断和预防工作提供信息。