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The Antidotal Activity of the Thiol Drug Diethyldithiocarbamate Against N-Acetyl-p-Benzoquinone Imine in Isolated Hepatocytes

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Biological Reactive Intermediates IV

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 283))

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Abstract

N-Acetyl-p-benzoquinone imine (NAPQI) is the putativereactive metabolite implicated in acetaminophenhepatotoxicity (Crocoran et al., Dahlin et al., Albano et al., and Rundgren et al.) which is a highly reactive electrophile as well as an oxidant (Rundgren et al.). Toxicity in isolated hepatocytes has been attibuted to the alkylation and/or oxidation of protein thiol groups (Albano et al. and Rundgren et al.).

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Abbreviations

DEDC:

diethyldithiocarbamate

DS:

disulfiram

DTT:

dithiothreitol

NAPQI:

N-Acetyl-p-Benzoquinone Imine

GSH:

reduced glutathione

GSSG:

oxidised glutathione

Hepes:

4-(2-hydroxyethyl)-1-piperazine-ethane-sulphonic acid

HPLC:

high performance liquid chromatography

FAB:

fast atom bombardment

Reference

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© 1991 Plenum Press, New York

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Lauriault, V.V., O’Brien, P.J. (1991). The Antidotal Activity of the Thiol Drug Diethyldithiocarbamate Against N-Acetyl-p-Benzoquinone Imine in Isolated Hepatocytes. In: Witmer, C.M., Snyder, R.R., Jollow, D.J., Kalf, G.F., Kocsis, J.J., Sipes, I.G. (eds) Biological Reactive Intermediates IV. Advances in Experimental Medicine and Biology, vol 283. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5877-0_38

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  • DOI: https://doi.org/10.1007/978-1-4684-5877-0_38

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4684-5879-4

  • Online ISBN: 978-1-4684-5877-0

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