| Literature DB >> 31730887 |
Sai Wu1, Huaixiang Liu1, Heping Zhao1, Xiaohui Wang1, Jingli Chen1, Dong Xia1, Chen Xiao1, Jianding Cheng2, Zhiqiang Zhao3, Yun He4.
Abstract
Alzheimer's disease (AD) is a neurodegenerative disease that can be induced by heavy metals such as lead. However, there is limited information on the role of blood-brain barrier (BBB) in lead induced AD-like pathology. This study investigates the potential mechanism of lead exposure aggravating the progression of Alzheimer's disease in mice through the BBB. 200 mg/L and 500 mg/L lead acetate were given to C57BL/6J and APP/PS1 mice through drinking water from a week before mating, until the offspring were 7-months-old. 8 female juvenile mice in each group were selected for this investigation. Lead exposure increased blood lead concentration which revealed the internal exposure level, accelerated Aβ1-42 deposition in APP/PS1 mouse cortexes and abnormal change in Zonula Occludin-1 (ZO-1) and Claudin-5 protein. It also increased the expression of p-tau in both the C57BL/6J and APP/PS1 mice, and decreased mRNA and protein expression in low-density lipoprotein receptor (LRP-1). Additionally, it increased the mRNA and protein expression of amyloid beta precursor protein (APP) and beta secretase 1 (BACE-1). The activated astrocytes increased in the brains of APP/PS1 mice, and coalesced around the Aβ1-42 deposition after lead exposure. The main vessels in deutocerebrum were attached with Aβ1-42 deposition. These results offer insight into the mechanism of preventing lead induced AD through cerebrovascular pathways.Entities:
Keywords: APP/PS1 gene; Alzheimer's disease; Blood-brain barrier; Lead
Year: 2019 PMID: 31730887 DOI: 10.1016/j.toxlet.2019.11.009
Source DB: PubMed Journal: Toxicol Lett ISSN: 0378-4274 Impact factor: 4.372