Air Pollution, Elevated Brain Iron and Alzheimer's Disease

空气污染、脑铁含量升高和阿尔茨海默病

• 批准号: 10285494
• 负责人: Deborah A Cory-Slechta
• 金额: $ 38.08万
• 依托单位: UNIVERSITY OF ROCHESTER
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-09-18 至 2025-06-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10285494
• 关键词: Adult; Affect; Aging; Air Pollution; Alzheimer' s Disease; Alzheimer' s disease patient; Alzheimer' s disease risk; Amygdaloid structure; Amyloid; Amyloid beta-Protein; Amyloid deposition; Area; Behavioral; Biological; Biological Models; Birth; Blood; Blood - brain barrier anatomy; Brain; Brain region; Bypass; Cell Count; Cerebrum; Cognitive; Copper; DNA Sequence Alteration; Data; Dementia; Disease; Environmental Risk Factor; Epidemiology; Etiology; Exposure to; Female; Funding; Geography; Grant; Health protection; Hippocampus (Brain); Histologic; Homeostasis; Human; Impaired cognition; Impairment; Inductively Coupled Plasma Mass Spectrometry; Inflammation; Inhalation; Inhalation Exposure; Iron; Lead levels; Link; Maps; Mediating; Memory; Meta-Analysis; Metals; Modeling; Mus; Nerve Degeneration; Neurodegenerative Disorders; Neurodevelopmental Disorder; Neurofibrillary Tangles; Neurons; Nose; Nucleus Accumbens; Olfactory Nerve; Olfactory dysfunction; Olfactory tract; Outcome Measure; Oxidation-Reduction; Oxidative Stress; Particulate Matter; Pathologic; Pathway interactions; Peripheral; Public Health; Regulation; Reporting; Risk Factors; Role; Schizophrenia; Senile Plaques; Sensorimotor functions; Sex Differences; Site; Stream; Suggestion; Synapses; Third Pregnancy Trimester; Time; Trigeminal nerve structure; abeta accumulation; air contaminant; air filter; behavior measurement; behavior test; disease phenotype; economic cost; epidemiology study; executive function; experimental study; fetal; geographic difference; high efficiency particulate air filter; in utero; macrophage; male; mortality; myelination; nanoparticle; nanoparticle exposure; neural network; neurodegenerative dementia; olfactory bulb; piriform cortex; postnatal; postnatal period; pre-clinical; sex; social; tau Proteins; ultrafine particle; uptake; virtual; young adult

ABSTRACT Numerous epidemiological studies have now linked air pollution (AP) with Alzheimer’s Disease (AD) and cognitive decline. Idiopathic AD, the most common form of dementia in the US, is a female-biased neurodegenerative disease of unknown etiology. In addition to the accumulation of plaques and tangles, AD is also characterized by marked elevations in brain levels of the redox active metal, iron (Fe), giving rise to a brain metal dyshomeostasis hypothesis for AD. The basis for the elevated Fe is not clear, but this supplement hypothesizes that exposures to Fe contamination from the ultrafine particle (UFP) component of AP, considered the most reactive component of AP, to which exposures can begin in utero and be lifelong following birth, contributes to the AD phenotype. Indeed, post-birth, such UFPs and associated contaminants move directly into blood stream, bypassing macrophages to each brain; UFPs can also be directly taken up into brain via olfactory and trigeminal nerves, bypassing the blood brain barrier. Our data from mice exposed via inhalation to concentrated ambient UFPs confirms significant elevation of brain Fe and alterations in other essential brain metals as well. Like most neurodegenerative diseases, AD is heterogeneous in expression which could reflect the geographical differences in the extent of Fe contamination. Interestingly, in that regard, the levels of highest Fe emissions in the U.S. overlap with areas of highest Alzheimer’s disease mortality. In preliminary data obtained from early postnatal exposures of both male and female mice, numerous female-specific features of AD have been seen: increased olfactory bulb microglial activation, consistent with nasal olfactory uptake, decreased trajectory of neuronal cell counts in nucleus accumbens, and increased levels of total hippocampal amyloids and tau at PND90. Ventriculomegaly, another feature seen in AD, was found in both sexes. The aim of this proposed supplement is to extend our current studies of AP-induced brain metal contamination, which to date has focused on neurodevelopmental disorders, to examine the effects of a 6 week exposure of adult mice to Fe UFPs at multiple time-points post exposure. Outcome measures will include neuropathological features of AD, specifically hyperphosphyorylated tau, beta amyloids, ventriculomegaly, myelination, and oxidative stress and ferroptosis, with behavioral measures of executive function. This supplement should establish a model that could be critical to defining mechanisms of AD and sex-related differences in vulnerability, as well as to provide data that is important to regulation of AP, and consequently to public health protection.

抽象的 许多流行病学研究现已将空气污染 (AP) 与阿尔茨海默病 (AD) 和 特发性 AD 是美国最常见的痴呆症，是一种女性偏向的痴呆症。 AD 是一种病因不明的神经退行性疾病。 其特征还在于大脑中氧化还原活性金属铁 (Fe) 的水平显着升高，从而导致 AD 的脑金属平衡失调假说 Fe 升高的基础尚不清楚，但这一点。 暴露于超细颗粒 (UFP) 的铁污染的补充剂 AP 的成分，被认为是 AP 中最具反应性的成分，可以开始接触 事实上，在出生后，这种 UFP 和出生后终生都会导致 AD 表型。 相关污染物直接进入血流，绕过巨噬细胞到达每个大脑； 也可以绕过血脑屏障，通过嗅觉和三叉神经直接进入大脑。 通过吸入暴露于浓缩环境 UFP 的小鼠的数据证实，脑铁含量显着升高 和大多数神经退行性疾病一样，AD 也会发生变化。 表达的异质性可以反映铁含量的地理差异 在这方面，美国的最高铁排放水平与污染地区重叠。 从产后早期接触这两种药物获得的初步数据显示，阿尔茨海默病死亡率最高。 在雄性和雌性小鼠中，发现了许多女性特有的 AD 特征：嗅球增加 小胶质细胞激活，与鼻嗅觉摄取一致，神经元细胞计数轨迹减少 PND90 时伏核、海马淀粉样蛋白和 tau 蛋白总量增加。 AD 中的另一个特征在两性中都有发现。本提议的补充的目的是扩展我们的研究范围。 目前对 AP 引起的脑金属污染的研究，迄今为止主要集中在神经发育 疾病，以检查成年小鼠在多个时间点接触 Fe UFP 6 周的影响 结果测量将包括 AD 的神经病理学特征，特别是过度磷酸化。 tau、β 淀粉样蛋白、脑室扩大、髓鞘形成、氧化应激和铁死亡，以及行为 该补充应建立一个对于定义执行功能至关重要的模型。 AD 的机制和与性别相关的脆弱性差异，并提供重要的数据 AP 的监管，从而保护公众健康。