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Title: Role of reactive metabolites in the circulation in extrahepatic toxicity.

Authors: Irving, Roy M; Elfarra, Adnan A

Published In Expert Opin Drug Metab Toxicol, (2012 Sep)

Abstract: Reactive metabolite-mediated toxicity is frequently limited to the organ where the electrophilic metabolites are generated. Some reactive metabolites, however, might have the ability to translocate from their site of formation. This suggests that for these reactive metabolites, investigations into the role of organs other than the one directly affected could be relevant to understanding the mechanism of toxicity. AREAS COVERED: The authors discuss the physiological and biochemical factors that can enable reactive metabolites to cause toxicity in an organ distal from the site of generation. Furthermore, the authors present a case study which describes studies that demonstrate that S-(1,2-dichlorovinyl)-L-cysteine sulfoxide (DCVCS) and N-acetyl-S-(1,2-dichlorovinyl-L-cysteine sulfoxide (N-AcDCVCS), reactive metabolites of the known trichloroethylene metabolites S-(1,2-dichlorovinyl)-L-cysteine (DCVC), and N-acetyl-S-(1,2-dichlorovinyl)-L-cysteine (N-AcDCVC), are generated in the liver and translocate through the circulation to the kidney to cause nephrotoxicity. EXPERT OPINION: The ability of reactive metabolites to translocate could be important to consider when investigating mechanisms of toxicity. A mechanistic approach, similar to the one described for DCVCS and N-AcDCVCS, could be useful in determining the role of circulating reactive metabolites in extrahepatic toxicity of drugs and other chemicals. If this is the case, intervention strategies that would not otherwise be feasible might be effective for reducing extrahepatic toxicity.

PubMed ID: 22681489 Exiting the NIEHS site

MeSH Terms: Acetylcysteine/analogs & derivatives; Acetylcysteine/blood; Acetylcysteine/metabolism; Acetylcysteine/toxicity; Cysteine/analogs & derivatives*; Cysteine/blood; Cysteine/metabolism; Cysteine/toxicity; Humans; Kidney/drug effects*; Kidney/metabolism; Kidney/pathology; Liver/drug effects*; Liver/metabolism; Liver/pathology; Trichloroethylene/blood; Trichloroethylene/metabolism; Trichloroethylene/toxicity

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