Current understanding of hexavalent chromium [Cr(VI)] neurotoxicity and new perspectives

• Published in: Environment international 2022-01, Vol.158, p.106877-106877, Article 106877
• Main Authors: Wise, John P., Young, Jamie L., Cai, Jun, Cai, Lu
• Format: Article
• Language: English
• Subjects: Animals; Brain; Chromium - toxicity; DNA Damage; Environmental Pollutants - toxicity; Glia; Hexavalent chromium; Metals; Mice; Neurotoxicity; Oxidative Stress
• ISSN: 0160-4120; 1873-6750
• DOI: 10.1016/j.envint.2021.106877

[Display omitted] •Cr(VI) is a major public health concern for neurotoxicity.•Cr(VI) literature suggests it does not contribute to brain cancers.•Cr(VI)( may contribute to etiology of autism spectrum disorder.•The highest Cr levels observed in human brain were in the pituitary and temporal lobe.•Animal studies show Cr(VI) induced widespread neurodegeneration and oxidative damage. Hexavalent chromium [Cr(VI)] is a global environmental pollutant that increases risk for several types of cancers and is increasingly being recognized as a neurotoxicant. Traditionally, the brain has been viewed as a largely post-mitotic organ due to its specialized composition of neurons, and consequently, clastogenic effects were not considered in neurotoxicology. Today, we understand the brain is composed of at least eight distinct cell types – most of which continue mitotic activity throughout lifespan. We have learned these dividing cells play essential roles in brain and body health. This review focuses on Cr(VI), a potent clastogen and known human carcinogen, as a potentially neurotoxic agent targeting mitotic cells of the brain. Despite its well-established role as a human carcinogen, Cr(VI) neurotoxicity studies have failed to find a significant link to brain cancers. In the few studies that did find a link, Cr(VI) was identified as a risk for gliomas. Instead, in the human brain, Cr(VI) appears to have more subtle deleterious effects that can impair childhood learning and attention development, olfactory function, social memory, and may contribute to motor neuron diseases. Studies of Cr(VI) neurotoxicity with animal and cell culture models have demonstrated elevated markers of oxidative damage and redox stress, with widespread neurodegeneration. One study showed mice exposed to Cr(VI)-laden tannery effluent exhibited longer periods of aggressive behavior toward an “intruder” mouse and took longer to recognize mice previously encountered, recapitulating the social memory deficits observed in humans. Here we conducted a critical review of the available literature on Cr(VI) neurotoxicity and synthesize the collective observations to thoroughly evaluate Cr(VI) neurotoxicity – much remains to be understood and recognized.