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Bioactivation to an aldehyde metabolite--possible role in the onset of toxicity induced by the anti-HIV drug abacavir.

Abstract
Aldehydes are highly reactive molecules, which can be generated during numerous physiological processes, including the biotransformation of drugs. Several non-P450 enzymes participate in their metabolism albeit alcohol dehydrogenase and aldehyde dehydrogenase are the ones most frequently involved in this process. Endogenous and exogenous aldehydes have been strongly implicated in multiple human pathologies. Their ability to react with biomacromolecules (e.g. proteins) yielding covalent adducts is suggested to be the common primary mechanism underlying the toxicity of these reactive species. Abacavir is one of the options for combined anti-HIV therapy. Although individual susceptibilities to adverse effects differ among patients, abacavir is associated with idiosyncratic hypersensitivity drug reactions and an increased risk of cardiac dysfunction. This review highlights the current knowledge on abacavir metabolism and discusses the potential role of bioactivation to an aldehyde metabolite, capable of forming protein adducts, in the onset of abacavir-induced toxic outcomes.
AuthorsNádia M Grilo, Catarina Charneira, Sofia A Pereira, Emília C Monteiro, M Matilde Marques, Alexandra M M Antunes
JournalToxicology letters (Toxicol Lett) Vol. 224 Issue 3 Pg. 416-23 (Jan 30 2014) ISSN: 1879-3169 [Electronic] Netherlands
PMID24211422 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
CopyrightCopyright © 2013 Elsevier Ireland Ltd. All rights reserved.
Chemical References
  • Aldehydes
  • Anti-HIV Agents
  • Dideoxynucleosides
  • abacavir
Topics
  • Aldehydes (metabolism)
  • Animals
  • Anti-HIV Agents (adverse effects, metabolism, toxicity)
  • Biotransformation
  • Dideoxynucleosides (adverse effects, metabolism, toxicity)
  • Drug Hypersensitivity (physiopathology)
  • Drug-Related Side Effects and Adverse Reactions
  • Heart Diseases (chemically induced, pathology)
  • Humans

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