» Articles » PMID: 36757557

Local and Systemic Hypoxia As Inductors of Increased Aluminum and Iron Brain Accumulation Promoting the Onset of Alzheimer's Disease

Overview
Date 2023 Feb 9
PMID 36757557
Authors
Affiliations
Soon will be listed here.
Abstract

Human environment is highly contaminated with aluminum, and aluminum is toxic to majority of tissues, particularly to neurons. In previous decades, aluminum exposure was frequently linked with the onset of Alzheimer's disease (AD), and increased levels of Al were detected in the brains of individuals with AD. People who live in a certain area are exposed to aluminum in a similar way (they eat the same vegetable and other foodstuffs, use similar cosmetics, and buy medications from the same manufacturer), nevertheless not all of them develop Alzheimer's disease. Majority of known risk factors for AD promote atherosclerosis and consequently reduce brain blood supply. In this review, we highlighted the significance of local (carotid disease and atherosclerosis of intracranial blood vessels) and systemic hypoxia (chronic obstructive pulmonary disease and anemia) in the development of AD. Nerve tissue is very sophisticated and sensitive to hypoxia and aluminum toxicity. As a side effect of compensatory mechanisms in case of hypoxia, neurons start to uptake aluminum and iron to a greater extent. This makes perfect a background for the gradual onset and development of AD.

Citing Articles

Association Between Hypoxia-Inducible Factor-1α and Neurological Diseases: A Bidirectional Two-Sample Mendelian Randomization Analysis.

Liang J, Du X, Wang M, Zheng H, Sun Y, Lin Y Brain Behav. 2025; 15(3):e70398.

PMID: 40022282 PMC: 11870835. DOI: 10.1002/brb3.70398.


Progressive iron overload in middle-aged mice impairs olfactory function, triggers lipid oxidation and induces apoptosis.

Deng L, Luo Q, Liu Y, Wang Y, Xiong Z, Wang H Front Pharmacol. 2025; 15:1506944.

PMID: 39749201 PMC: 11693683. DOI: 10.3389/fphar.2024.1506944.


Association of Plasma Claudin-5 with Age and Alzheimer Disease.

Tachibana K, Hirayama R, Sato N, Hattori K, Kato T, Takeda H Int J Mol Sci. 2024; 25(3).

PMID: 38338697 PMC: 10855409. DOI: 10.3390/ijms25031419.


Interference of Parenteral Nutrition Components in Silicon-Mediated Protection Against Aluminum Bioaccumulation.

Noremberg Kunz S, Bohrer D, do Nascimento P, Cibin F, de Carvalho L Biol Trace Elem Res. 2023; 202(8):3662-3671.

PMID: 37924413 DOI: 10.1007/s12011-023-03929-0.

References
1.
Plassman B, Langa K, Fisher G, Heeringa S, Weir D, Ofstedal M . Prevalence of dementia in the United States: the aging, demographics, and memory study. Neuroepidemiology. 2007; 29(1-2):125-32. PMC: 2705925. DOI: 10.1159/000109998. View

2.
Jurcovicova J . Glucose transport in brain - effect of inflammation. Endocr Regul. 2014; 48(1):35-48. DOI: 10.4149/endo_2014_01_35. View

3.
Fernandes R, Goncalves Correa M, Aragao W, Nascimento P, Cartagenes S, Rodrigues C . Preclinical evidences of aluminum-induced neurotoxicity in hippocampus and pre-frontal cortex of rats exposed to low doses. Ecotoxicol Environ Saf. 2020; 206:111139. DOI: 10.1016/j.ecoenv.2020.111139. View

4.
Mladenovic J . Aluminum inhibits erythropoiesis in vitro. J Clin Invest. 1988; 81(6):1661-5. PMC: 442607. DOI: 10.1172/JCI113502. View

5.
Yuan C, Lee Y, Hsu G . Aluminum overload increases oxidative stress in four functional brain areas of neonatal rats. J Biomed Sci. 2012; 19:51. PMC: 3404950. DOI: 10.1186/1423-0127-19-51. View