Impact of Prenatal alcohol on Alzheimer's disease related pathology and cognitive impairment

产前酒精对阿尔茨海默病相关病理和认知障碍的影响

• 批准号: 10387300
• 负责人: Rajesh C Miranda
• 金额: $ 21.41万
• 依托单位: TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR
• 依托单位国家: 美国
• 财政年份: 2022
• 资助国家: 美国
• 起止时间: 2022-02-10 至 2024-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10387300
• 关键词: Acute; Address; Adult; Affect; Age; Age-Months; Aging; Alcohol abuse; Alcoholism; Alcohols; Alzheimer' s Disease; Alzheimer' s disease pathology; Alzheimer' s disease risk; American; Anatomy; Animal Model; Appearance; Area; Astrocytosis; Behavior; Behavioral; Behavioral Assay; Biological; Biological Assay; Blood Vessels; Blood flow; Brain; Cardiovascular Diseases; Cardiovascular system; Caring; Cephalic; Cerebrovascular Disorders; Chronic; Cognitive deficits; Collaborations; Data; Dementia; Disease; Disease susceptibility; Encephalitis; Exhibits; Exons; Exposure to; Female; Fetal Alcohol Exposure; Fetal Alcohol Spectrum Disorder; First Pregnancy Trimester; Foundations; Functional disorder; Future; Goals; Health; Heart Hypertrophy; Histologic; Human; Human Amyloid Precursor Protein; Hypertension; Impaired cognition; Impairment; Individual; Inflammation; Institutes; Intervention; Kidney Failure; Knowledge; Lesion; Life; Life Experience; Link; Longevity; Maternal Exposure; Measures; Mental Depression; Metabolic; Metabolic Diseases; Mission; Modeling; Mus; Mutation; Nerve Degeneration; Neurocognitive Deficit; Neurodegenerative Disorders; Neurofibrillary Tangles; Neurologic; Non-Insulin-Dependent Diabetes Mellitus; Outcome Study; Pathogenicity; Pathology; Persons; Phenotype; Predisposition; Premature Mortality; Premature aging syndrome; Rattus; Recording of previous events; Recovery of Function; Reporting; Research Personnel; Risk; Risk Factors; Rodent; Rodent Model; Senile Plaques; Social Interaction; Swedish mutation; Teenagers; Testing; Transgenes; Transgenic Organisms; Ultrasonography; age related; alcohol prevention; alcohol related consequences; behavioral impairment; cerebrovascular; clinical care; cognitive function; dementia risk; depressive symptoms; disability; disorder risk; early life adversity; early onset; experience; familial Alzheimer disease; fetal; hypertensive; hypoperfusion; innovation; ischemic injury; male; middle age; mouse model; neurobehavioral; novel; object recognition; offspring; prenatal; presenilin-1; social; trend; vapor; virtual; young adult

Project Summary: Persons with fetal alcohol spectrum disorders (FASD) experience life-long neurocognitive deficits as well as social and adaptive dysfunction, but we know virtually nothing about their health as they age. We recently reported that prenatal alcohol-exposure (PAE) resulted in long-term alteration in cranially-directed blood flow and reduced recovery of function after an acute ischemic injury in adulthood. This suggests that PAE is an important risk factor for cerebrovascular diseases and consequently, for dementia and Alzheimer's disease (AD). Young PAE rats also exhibit cognitive deficits and importantly, increased depression-related behaviors which are early predictors of AD. Therefore, in these studies, we will utilize the transgenic TgF344-AD rat which develops AD pathology in aging, to test the hypothesis that PAE will accelerate cerebro-vascular impairment, behavioral dysfunction and the accumulation of AD-related brain lesions, leading to premature aging. Moreover, we will specifically test whether male and female PAE offspring differ in their accumulation of AD-related anatomical and neurobehavioral pathology. We will implement a vapor-chamber model of repeated PAE, to achieve consistent binge-like maternal exposure episodes, spanning the fetal neurogenic period. PAE and control offspring will be assessed from young adults to 15 months of age, by ultrasound imaging of cranially directed blood flow, by a panel of behavioral assays for cognitive dysfunction and depression-like phenotypes, as well as a panel of histological assays for AD pathology. The investigators have a history of collaboration and application of experimental rigor in their areas of complementary expertise in models of aging and PAE, which supports the feasibility of the proposed studies. These studies are significant because they address a critical knowledge gap about the link between early life adversity, i.e., PAE, and the onset of AD. We expect that, if these studies do link PAE to accelerated AD pathology, they will help redefine FASD as a disorder of premature aging and strengthen the premise for investigating mechanisms that link PAE to aging, as well as interventions that decouple this linkage.

项目概要： 患有胎儿酒精谱系障碍 (FASD) 的人会经历终生的神经认知缺陷以及 社交和适应功能障碍，但我们对他们随着年龄增长的健康状况几乎一无所知。我们最近 报道称，产前酒精暴露（PAE）导致颅脑血流的长期改变 成年期急性缺血性损伤后功能恢复减少。这表明 PAE 是 脑血管疾病的重要危险因素，因此也是痴呆和阿尔茨海默氏病的重要危险因素 （广告）。年轻的 PAE 大鼠还表现出认知缺陷，更重要的是，抑郁相关行为增加 这是 AD 的早期预测因子。因此，在这些研究中，我们将利用转基因 TgF344-AD 大鼠 该研究开发了衰老过程中的 AD 病理学，以检验 PAE 会加速脑血管损伤的假设 损害、行为功能障碍以及 AD 相关脑部病变的积累，导致早产 老化。此外，我们将专门测试雄性和雌性PAE后代在积累方面是否存在差异 AD 相关的解剖学和神经行为病理学。我们将实施一个均热板模型 重复 PAE，以实现一致的暴食样母体暴露事件，跨越胎儿神经源性 时期。 PAE 和对照后代将从青壮年到 15 个月大，通过超声波进行评估 通过一组针对认知功能障碍的行为分析对颅内定向血流进行成像 抑郁症样表型，以及 AD 病理学的一组组织学检测。 研究人员在各自的领域有着合作和严格实验应用的历史 衰老模型和 PAE 方面的互补专业知识支持了拟议研究的可行性。 这些研究意义重大，因为它们解决了关于早期生活与生命之间联系的关键知识差距。 逆境，即 PAE 和 AD 的发作。我们预计，如果这些研究确实将 PAE 与加速 AD 联系起来 病理学上，它们将有助于将 FASD 重新定义为一种过早衰老的疾病，并强化了 研究 PAE 与衰老之间的联系机制，以及消除这种联系的干预措施。