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PMID: 1567465 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The metabolism of aminoacetone to methylglyoxal by semicarbazide-sensitive amine oxidase in human umbilical artery.

Biochemical pharmacology ·Vol. 43 ·No. 7 ·1992-04-01 ·Pages 1409-14

Lyles GA, Chalmers J

Abstract

The aliphatic amine aminoacetone has been described previously as a product of mitochondrial metabolism of threonine and glycine. Here, aminoacetone is shown to be deaminated to methylglyoxal by supernatants obtained by low speed centrifugation (600 g/10 min) of human umbilical artery homogenates, and also by membrane fractions isolated by high speed centrifugation (105,000 g/60 min) of these supernatants. Metabolism of 100 microM aminoacetone was completely inhibited by 1 mM propargylamine and MDL 72145, drugs which are capable of inhibiting the membrane-bound semicarbazide-sensitive amine oxidase (SSAO) activity found in vascular smooth muscle cells, whereas 1 mM pargyline and deprenyl which are inhibitors of monoamine oxidase, were without inhibitory effect. Estimated kinetic constants (at pH 7.8) for aminoacetone metabolism were Km = 92 microM; Vmax = 270 nmol/hr/mg protein. In addition, aminoacetone was a competitive inhibitor (Ki = 83 microM and 128 microM in low speed supernatants and high speed membrane fractions, respectively) of [14C]benzylamine metabolism by SSAO in this tissue. Aminoacetone would appear to be an endogenously occurring amine with a Km for metabolism by SSAO far lower than other aliphatic and aromatic biogenic amines examined previously as potential physiological substrates for the human vascular enzyme and possible implications of this are discussed.

MeSH Terms
Acetone/analogs & derivatives,metabolism Amine Oxidase (Copper-Containing) Benzylamines/metabolism Humans Kinetics Oxidoreductases Acting on CH-NH Group Donors/antagonists & inhibitors,metabolism Pyruvaldehyde/metabolism Semicarbazides/pharmacology Umbilical Arteries/drug effects,enzymology
Chemicals
Benzylamines Semicarbazides Acetone carbamylhydrazine Pyruvaldehyde benzylamine Amine Oxidase (Copper-Containing) Oxidoreductases Acting on CH-NH Group Donors aminoacetone
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lyles G A
Department of Pharmacology, Ninewells Hospital and Medical School, University of Dundee, U.K.
Chalmers J
Article Info
Journal
Biochemical pharmacology
Abbr.
Biochem Pharmacol
ISSN
0006-2952
Published
1992-04-01
Pages
1409-14
Language
English
Region
England
NLM ID
0101032
Subset
IM
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