Literature DB >> 7121616

The cellular location of catechol-O-methyltransferase in rat liver.

M J Raxworthy, P A Gulliver, P J Hughes.   

Abstract

Catechol-O-methyltransferase (COMT) activity on the extracellular face of the plasma membrane of isolated rat hepatocytes was assayed, and 4.3% of total COMT activity was located there in cells which satisfied our criteria of viability. However, since 1.2% of the cells' lactate dehydrogenase activity was also apparently extracellular, and this proportion increased to 3.4% under the conditions of the COMT assay the amounts of extracellular COMT may be even less. COMT in rat liver microsomes and plasma membranes represent 2.3% and 0.08% of total rat liver COMT respectively. This implies an insignificant role for plasma membrane COMT although reported altered kinetic behaviour could elevate microsomal COMT to a supporting role in the regulation of catecholamine concentration in the circulation. Since by far the largest fraction of COMT is located intracellularly in the soluble cell fraction, the physiological functions of COMT seem to be dependent on the passage of substrates through the cell membrane for their presentation to the enzyme.

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Year:  1982        PMID: 7121616     DOI: 10.1007/bf00506319

Source DB:  PubMed          Journal:  Naunyn Schmiedebergs Arch Pharmacol        ISSN: 0028-1298            Impact factor:   3.000


  33 in total

1.  Selective identification of "true" beta-adrenergic receptors in the plasma membranes of rat adipocytes.

Authors:  J Pairault; M H Laudat
Journal:  FEBS Lett       Date:  1975-01-15       Impact factor: 4.124

2.  Transmural and subcellular localization of monoamine oxidase and catechol-0-methyl transferase in rabbit aorta.

Authors:  M A Verity; C Su; J A Bevan
Journal:  Biochem Pharmacol       Date:  1972-01-15       Impact factor: 5.858

3.  Transient-kinetic studies of pig muscle lactate dehydrogenase.

Authors:  R A Stinson; H Gutfreund
Journal:  Biochem J       Date:  1971-01       Impact factor: 3.857

4.  Re-evaluation of the relationship between catechol-O-methyl transferase and the binding of norepinephrine to brown adipocyte membranes.

Authors:  J Durand; J P Giacobino; J Deshusses; L Girardier
Journal:  Biochem Pharmacol       Date:  1979-04-15       Impact factor: 5.858

5.  The purification and kinetic properties of liver microsomal-catechol-o-methyltransferase.

Authors:  R T Borchardt; C F Cheng; P H Cooke
Journal:  Life Sci       Date:  1974-03-16       Impact factor: 5.037

6.  The action of adenosine deaminase on S-adenosylhomocysteine and related compounds.

Authors:  F Schlenk; C R Zydek
Journal:  Biochem Biophys Res Commun       Date:  1968-05-10       Impact factor: 3.575

Review 7.  Methylation reactions in the formation and metabolism of catecholamines and other biogenic amines.

Authors:  J Axelrod
Journal:  Pharmacol Rev       Date:  1966-03       Impact factor: 25.468

8.  Factors affecting the enzymatic formation of O-methylated dihydroxy derivatives.

Authors:  J K Inscoe; J Daly; J Axelrod
Journal:  Biochem Pharmacol       Date:  1965-08       Impact factor: 5.858

9.  O-Methylation of 3H-norepinephrine by epididymal adipose tissue.

Authors:  G J Traiger; D N Calvert
Journal:  Biochem Pharmacol       Date:  1969-01       Impact factor: 5.858

10.  Extensive conjugation of dopamine (3,4-dihydroxyphenethylamine) metabolites in cultured human skin fibroblasts and rat hepatoma cells.

Authors:  P A Crooks; X O Breakefield; C H Sulens; C M Castiglione; J K Coward
Journal:  Biochem J       Date:  1978-10-15       Impact factor: 3.857

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