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Methodology to assay CYP2E1 mixed function oxidase catalytic activity and its induction

The cytochrome P450 mixed function oxidase enzymes are the major catalysts involved in drug metabolism. There are many forms of P450. CYP2E1 metabolizes many toxicologically important compounds including ethanol and is active in generating reactive oxygen species. Since several of the contributions...

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Autor principal: Cederbaum, Arthur I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297943/
https://www.ncbi.nlm.nih.gov/pubmed/25454746
http://dx.doi.org/10.1016/j.redox.2014.09.007
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author Cederbaum, Arthur I.
author_facet Cederbaum, Arthur I.
author_sort Cederbaum, Arthur I.
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description The cytochrome P450 mixed function oxidase enzymes are the major catalysts involved in drug metabolism. There are many forms of P450. CYP2E1 metabolizes many toxicologically important compounds including ethanol and is active in generating reactive oxygen species. Since several of the contributions in the common theme series “Role of CYP2E1 and Oxidative/Nitrosative Stress in the Hepatotoxic Actions of Alcohol” discuss CYP2E1, this methodology review describes assays on how CYP2E1 catalytic activity and its induction by ethanol and other inducers can be measured using substrate probes such as the oxidation of para-nitrophenol to para-nitrocatechol and the oxidation of ethanol to acetaldehyde. Approaches to validate that a particular reaction e.g. oxidation of a drug or toxin is catalyzed by CYP2E1 or that induction of that reaction is due to induction of CYP2E1 are important and specific examples using inhibitors of CYP2E1, anti-CYP2E1 IgG or CYP2E1 knockout and knockin mice will be discussed.
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spelling pubmed-42979432015-01-21 Methodology to assay CYP2E1 mixed function oxidase catalytic activity and its induction Cederbaum, Arthur I. Redox Biol Article The cytochrome P450 mixed function oxidase enzymes are the major catalysts involved in drug metabolism. There are many forms of P450. CYP2E1 metabolizes many toxicologically important compounds including ethanol and is active in generating reactive oxygen species. Since several of the contributions in the common theme series “Role of CYP2E1 and Oxidative/Nitrosative Stress in the Hepatotoxic Actions of Alcohol” discuss CYP2E1, this methodology review describes assays on how CYP2E1 catalytic activity and its induction by ethanol and other inducers can be measured using substrate probes such as the oxidation of para-nitrophenol to para-nitrocatechol and the oxidation of ethanol to acetaldehyde. Approaches to validate that a particular reaction e.g. oxidation of a drug or toxin is catalyzed by CYP2E1 or that induction of that reaction is due to induction of CYP2E1 are important and specific examples using inhibitors of CYP2E1, anti-CYP2E1 IgG or CYP2E1 knockout and knockin mice will be discussed. Elsevier 2014-10-06 /pmc/articles/PMC4297943/ /pubmed/25454746 http://dx.doi.org/10.1016/j.redox.2014.09.007 Text en © 2014 The Author http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Cederbaum, Arthur I.
Methodology to assay CYP2E1 mixed function oxidase catalytic activity and its induction
title Methodology to assay CYP2E1 mixed function oxidase catalytic activity and its induction
title_full Methodology to assay CYP2E1 mixed function oxidase catalytic activity and its induction
title_fullStr Methodology to assay CYP2E1 mixed function oxidase catalytic activity and its induction
title_full_unstemmed Methodology to assay CYP2E1 mixed function oxidase catalytic activity and its induction
title_short Methodology to assay CYP2E1 mixed function oxidase catalytic activity and its induction
title_sort methodology to assay cyp2e1 mixed function oxidase catalytic activity and its induction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297943/
https://www.ncbi.nlm.nih.gov/pubmed/25454746
http://dx.doi.org/10.1016/j.redox.2014.09.007
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