The aging brain: impact of heavy metal neurotoxicity.
Omamuyovwi Meashack IjomoneChibuzor W IfenatuohaOritoke M AlukoOlayemi K IjomoneMichael AschnerPublished in: Critical reviews in toxicology (2020)
The aging process is accompanied by critical changes in cellular and molecular functions, which upset the homeostatic balance in the central nervous system. Accumulation of metals renders the brain susceptible to neurotoxic insults by mechanisms such as mitochondrial dysfunction, neuronal calcium-ion dyshomeostasis, buildup of damaged molecules, compromised DNA repair, reduction in neurogenesis, and impaired energy metabolism. These hallmarks have been identified to be responsible for neuronal injuries, resulting in several neurological disorders. Various studies have shown solid associations between metal accumulation, abnormal protein expressions, and pathogenesis of neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, Huntington's disease, and Amyotrophic lateral sclerosis. This review highlights metals (such as manganese, zinc, iron, copper, and nickel) for their accumulation, and consequences in the development of neurological disorders, in relation to the aging brain.
Keyphrases
- cerebral ischemia
- dna repair
- amyotrophic lateral sclerosis
- resting state
- white matter
- heavy metals
- oxide nanoparticles
- subarachnoid hemorrhage
- health risk
- functional connectivity
- blood brain barrier
- health risk assessment
- brain injury
- human health
- cognitive decline
- risk assessment
- oxidative stress
- mild cognitive impairment