Oxidative stress in MeHg-induced neurotoxicity

Marcelo Farina, Michael Aschner, João B T Rocha

Research output: Contribution to journalReview article

178 Citations (Scopus)

Abstract

Methylmercury (MeHg) is an environmental toxicant that leads to long-lasting neurological and developmental deficits in animals and humans. Although the molecular mechanisms mediating MeHg-induced neurotoxicity are not completely understood, several lines of evidence indicate that oxidative stress represents a critical event related to the neurotoxic effects elicited by this toxicant. The objective of this review is to summarize and discuss data from experimental and epidemiological studies that have been important in clarifying the molecular events which mediate MeHg-induced oxidative damage and, consequently, toxicity. Although unanswered questions remain, the electrophilic properties of MeHg and its ability to oxidize thiols have been reported to play decisive roles to the oxidative consequences observed after MeHg exposure. However, a close examination of the relationship between low levels of MeHg necessary to induce oxidative stress and the high amounts of sulfhydryl-containing antioxidants in mammalian cells (e.g., glutathione) have led to the hypothesis that nucleophilic groups with extremely high affinities for MeHg (e.g., selenols) might represent primary targets in MeHg-induced oxidative stress. Indeed, the inhibition of antioxidant selenoproteins during MeHg poisoning in experimental animals has corroborated this hypothesis. The levels of different reactive species (superoxide anion, hydrogen peroxide and nitric oxide) have been reported to be increased in MeHg-exposed systems, and the mechanisms concerning these increments seem to involve a complex sequence of cascading molecular events, such as mitochondrial dysfunction, excitotoxicity, intracellular calcium dyshomeostasis and decreased antioxidant capacity. This review also discusses potential therapeutic strategies to counteract MeHg-induced toxicity and oxidative stress, emphasizing the use of organic selenocompounds, which generally present higher affinity for MeHg when compared to the classically studied agents.

Original languageEnglish (US)
Pages (from-to)405-417
Number of pages13
JournalToxicology and Applied Pharmacology
Volume256
Issue number3
DOIs
StatePublished - 2011
Externally publishedYes

Fingerprint

Oxidative stress
Oxidative Stress
Antioxidants
Toxicity
Animals
Selenoproteins
Sulfhydryl Compounds
Superoxides
Poisoning
Hydrogen Peroxide
Glutathione
Epidemiologic Studies
Nitric Oxide
Cells
Calcium
Water
Therapeutics

Keywords

  • Glutamate
  • Methylmercury
  • Neurotoxicity
  • Oxidative stress
  • Selenol
  • Selenoproteins
  • Thiol

ASJC Scopus subject areas

  • Medicine(all)
  • Toxicology
  • Pharmacology

Cite this

Oxidative stress in MeHg-induced neurotoxicity. / Farina, Marcelo; Aschner, Michael; Rocha, João B T.

In: Toxicology and Applied Pharmacology, Vol. 256, No. 3, 2011, p. 405-417.

Research output: Contribution to journalReview article

Farina, Marcelo ; Aschner, Michael ; Rocha, João B T. / Oxidative stress in MeHg-induced neurotoxicity. In: Toxicology and Applied Pharmacology. 2011 ; Vol. 256, No. 3. pp. 405-417.
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