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Preparation and Characterisation of S9 Fractions

Susan A. Hubbard, T.M. Brooks, L. P. Gonzalez, James Winfred Bridges

Open publisher page 13 citations

Abstract

Many xenobiotics are only mutagenic after metabolism by the drug metabolising enzymes. Attention has focused on one of these enzymes ‘cytochrome P450’ (a generic term for a group of haem containing mixed function oxidase isoenzymes). Since the profile of metabolites produced by each isoenzyme is different and the activity of each isoenzyme is affected by the species, sex, age, health and environmental exposure of the animals used and by the tissue selected it is important to identify any factors which may affect their bioactivation when added to in vitro mutagenicity tests such as the Ames test. Metabolic activation of mutagens in vitro is generally achieved by supplementing the system by the addition of a mammalian microsome preparation, usually in the form of 9000 g supernatant (S9) from rodent liver. This fraction contains the Cyt. P450 enzymes as well as cytosolic enzymes. These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

About this research paper

What this paper is about

Many xenobiotics are only mutagenic after metabolism by the drug metabolising enzymes. Attention has focused on one of these enzymes ‘cytochrome P450’ (a generic term for a group of haem containing mixed function oxidase isoenzymes). Since the profile of metabolites produced by each isoenzyme is different and the activity of each isoenzyme is affected by the species, sex, age, health and environmental exposure of the animals used and by the tissue selected it is important to identify any factors which may affect their bioactivation when added to in vitro mutagenicity tests such as the Ames test. Metabolic activation of mutagens in vitro is generally achieved by supplementing the system by the addition of a mammalian microsome preparation, usually in the form of 9000 g supernatant (S9) from rodent liver. This fraction contains the Cyt. P450 enzymes as well as cytosolic enzymes. These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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OpenAlex reports 13 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Many xenobiotics are only mutagenic after metabolism by the drug metabolising enzymes. Attention has focused on one of these enzymes ‘cytochrome P450’ (a generic term for a group of haem containing mixed function oxidase isoenzymes). Since the profile of metabolites produced by each isoenzyme is different and the activity of each isoenzyme is affected by the species, sex, age, health and environmental exposure of the animals used and by the tissue selected it is important to identify any factors which may affect their bioactivation when added to in vitro mutagenicity tests such as the Ames test. Metabolic activation of mutagens in vitro is generally achieved by supplementing the system by the addition of a mammalian microsome preparation, usually in the form of 9000 g supernatant (S9) from rodent liver. This fraction contains the Cyt. P450 enzymes as well as cytosolic enzymes. These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Key concepts: Isozyme, Microsome, S9 fraction, Xenobiotic, Cytochrome P450, Enzyme, Biochemistry, Mixed Function Oxidase

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