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慢性暴露于环境交通相关空气污染对野生型和遗传易感性雄性和雌性大鼠阿尔茨海默病表型的影响。

The Effects of Chronic Exposure to Ambient Traffic-Related Air Pollution on Alzheimer's Disease Phenotypes in Wildtype and Genetically Predisposed Male and Female Rats.

机构信息

Department of Molecular Biosciences, University of California Davis (UC Davis) School of Veterinary Medicine, Davis, California, USA.

Air Quality Research Center, UC Davis, Davis, California, USA.

出版信息

Environ Health Perspect. 2021 May;129(5):57005. doi: 10.1289/EHP8905. Epub 2021 May 10.

Abstract

BACKGROUND

Epidemiological data link traffic-related air pollution (TRAP) to increased risk of Alzheimer's disease (AD). Preclinical data corroborating this association are largely from studies of male animals exposed acutely or subchronically to high levels of isolated fractions of TRAP. What remains unclear is whether chronic exposure to ambient TRAP modifies AD risk and the influence of sex on this interaction.

OBJECTIVES

This study sought to assess effects of chronic exposure to ambient TRAP on the time to onset and severity of AD phenotypes in a preclinical model and to determine whether sex or genetic susceptibility influences outcomes.

METHODS

Male and female TgF344-AD rats that express human AD risk genes and wildtype littermates were housed in a vivarium adjacent to a heavily trafficked tunnel in Northern California and exposed for up to 14 months to filtered air (FA) or TRAP drawn from the tunnel and delivered to animals unchanged in real time. Refractive particles in the brain and AD phenotypes were quantified in 3-, 6-, 10-, and 15-month-old animals using hyperspectral imaging, behavioral testing, and neuropathologic measures.

RESULTS

Particulate matter (PM) concentrations in TRAP exposure chambers fluctuated with traffic flow but remained below 24-h PM with aerodynamic diameter less than or equal to 2.5 micrometers () U.S. National Ambient Air Quality Standards limits. Ultrafine PM was a predominant component of TRAP. Nano-sized refractive particles were detected in the hippocampus of TRAP animals. TRAP-exposed animals had more amyloid plaque deposition, higher hyperphosphorylated tau levels, more neuronal cell loss, and greater cognitive deficits in an age-, genotype-, and sex-dependent manner. TRAP-exposed animals also had more microglial cell activation, but not astrogliosis.

DISCUSSION

These data demonstrate that chronic exposure to ambient TRAP promoted AD phenotypes in wildtype and genetically susceptible rats. TRAP effects varied according to age, sex, and genotype, suggesting that AD progression depends on complex interactions between environment and genetics. These findings suggest current regulations are insufficient to protect the aging brain. https://doi.org/10.1289/EHP8905.

摘要

背景

流行病学数据将与交通相关的空气污染(TRAP)与阿尔茨海默病(AD)的风险增加联系起来。支持这种关联的临床前数据主要来自于急性或亚慢性暴露于 TRAP 分离分数的雄性动物研究。目前尚不清楚的是,慢性暴露于环境 TRAP 是否会改变 AD 风险,以及性别对这种相互作用的影响。

目的

本研究旨在评估慢性暴露于环境 TRAP 对临床前模型中 AD 表型发病时间和严重程度的影响,并确定性别或遗传易感性是否影响结果。

方法

雄性和雌性 TgF344-AD 大鼠表达人类 AD 风险基因,与其野生型同窝仔鼠一起饲养在加利福尼亚州北部一个靠近交通繁忙隧道的动物房舍中,并在长达 14 个月的时间内暴露于过滤空气(FA)或从隧道中提取并实时输送到动物体内的 TRAP。使用高光谱成像、行为测试和神经病理学测量,在 3、6、10 和 15 个月大的动物中定量分析大脑中的折射颗粒和 AD 表型。

结果

TRAP 暴露室中的颗粒物(PM)浓度随交通流量波动,但仍低于 24 小时 PM ,空气动力学直径小于或等于 2.5 微米()美国国家环境空气质量标准限制。超细 PM 是 TRAP 的主要成分。在 TRAP 动物的海马区检测到纳米级折射颗粒。TRAP 暴露动物表现出与年龄、基因型和性别相关的淀粉样斑块沉积增加、磷酸化 tau 水平升高、神经元细胞丢失增加和认知缺陷更严重。TRAP 暴露动物也有更多的小胶质细胞激活,但没有星形胶质细胞增生。

讨论

这些数据表明,慢性暴露于环境 TRAP 促进了野生型和遗传易感大鼠的 AD 表型。TRAP 的影响因年龄、性别和基因型而异,表明 AD 进展取决于环境和遗传之间的复杂相互作用。这些发现表明,目前的规定不足以保护衰老的大脑。https://doi.org/10.1289/EHP8905.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ac5/8110309/ffdfd3913e4d/ehp8905_f1.jpg

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