4.7 Article

Global Proteomic Profile of Aluminum-Induced Hippocampal Impairments in Rats: Are Low Doses of Aluminum Really Safe?

Journal

Publisher

MDPI
DOI: 10.3390/ijms232012523

Keywords

aluminum; hippocampus; neurotoxicity

Funding

  1. Fundacao Amazonia de Amparo a Estudos e Pesquisas (FAPESPA) [15/2021]
  2. Brazilian National Council for Scientific and Technological Development (CNPq) from the Brazilian Ministry of Science, Technology, and Innovation
  3. Coordination for the Improvement of Higher Education Personnel (CAPES) [001]
  4. FAPESPA
  5. CNPq [312275/2021-8]
  6. Pro-Reitoria de Pesquisa e Pos-Graduacao from the Federal University of Para

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This study found that exposure to low doses of aluminum chloride can lead to reduced learning and memory abilities, which is associated with dysregulated protein expression and decreased cell body density in the hippocampus.
Hippocampus is the brain area where aluminum (Al) accumulates in abundance and is widely associated with learning and memory. In the present study, we evaluate behavioral, tissue, and proteomic changes in the hippocampus of Wistar rats caused by exposure to doses that mimic human consumption of aluminum chloride (AlCl3) in urban areas. For this, male Wistar rats were divided into two groups: Control (distilled water) and AlCl3 (8.3 mg/kg/day), both groups were exposed orally for 60 days. After the Al exposure protocol, cognitive functions were assessed by the Water maze test, followed by a collection for analysis of the global proteomic profile of the hippocampus by mass spectrometry. Aside from proteomic analysis, we performed a histological analysis of the hippocampus, to the determination of cell body density by cresyl violet staining in Cornu Ammonis fields (CA) 1 and 3, and hilus regions. Our results indicated that exposure to low doses of aluminum chloride triggered a decreased cognitive performance in learning and memory, being associated with the deregulation of proteins expression, mainly those related to the regulation of the cytoskeleton, cellular metabolism, mitochondrial activity, redox regulation, nervous system regulation, and synaptic signaling, reduced cell body density in CA1, CA3, and hilus.

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