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PMID: 3923382 Published · ppublish English Journal Article

Polyamine reutilization and turnover in brain.

Neurochemical research ·Vol. 10 ·No. 4 ·1985-04-00 ·Pages 529-44

Seiler N, Bolkenius FN

Abstract

N1,N2-bis-(2,3-butadienyl)-1,4-butanediamine (MDL 72527) is an irreversible, specific inhibitor of polyamine oxidase, which allows one to completely inactivate this enzyme in all organs of an experimental animal. As a result one observes a linear increase of N1-acetylspermidine and N1-acetylspermine concentrations in brain. The rate of accumulation seems directly proportional to the rate of spermidine, and spermine degradation respectively, and since no compensatory changes of the polyamine synthetic enzymes were induced by inhibition of polyamine oxidase, the rate of acetyl-polyamine accumulation is assumed to be a measure for polyamine turnover. The decrease of brain putrescine levels by 70 percent in the brains of MDL 72527-treated animals suggests the quantitative significance of putrescine reutilisation. Pretreatment of the animals with D,L-alpha-difluoromethylornithine, an irreversible inhibitor of ornithine decarboxylase reduced both, polyamine turnover rate and the extent of putrescine reutilization. Inhibition of GABA-T produced a significant increase of polyamine turnover in brain, in agreement with the known induction of ornithine decarboxylase activity after treatment with inhibitors of GABA-T.

MeSH Terms
Alkynes Aminocaproates/pharmacology Animals Brain/metabolism Brain Chemistry/drug effects Eflornithine Male Mice Ornithine/analogs & derivatives,pharmacology Oxidoreductases Acting on CH-NH Group Donors/antagonists & inhibitors Polyamines/metabolism Spermidine/analogs & derivatives,analysis Spermine/analogs & derivatives,analysis Vigabatrin
Chemicals
Alkynes Aminocaproates Polyamines N(1)-acetylspermidine N'-acetylspermine Spermine 4-amino-5-hexynoic acid Ornithine Oxidoreductases Acting on CH-NH Group Donors polyamine oxidase Vigabatrin Spermidine Eflornithine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Seiler N
Bolkenius F N
References (22)
22 references, click to expand
  1. Decreased protein-synthetic activity is an early consequence of spermidine depletion in rat hepatoma tissue-culture cells.
    Biochem J. 1984 Feb 1;217(3):731-41 PMID: 6424650
  2. Polyamine biosynthesis and interconversion in rodent tissues.
    Fed Proc. 1982 Dec;41(14):3065-72 PMID: 7141002
  3. IDENTIFICATION OF THE AMINOALDEHYDES PRODUCED BY THE OXIDATION OF SPERMINE AND SPERMIDINE WITH PURIFIED PLASMA AMINE OXIDASE.
    J Biol Chem. 1964 Jul;239:2194-203 PMID: 14209948
  4. On the turnover of polyamines spermidine and spermine in mouse brain and other organs.
    Neurochem Res. 1980 Feb;5(2):123-43 PMID: 7366798
  5. gamma-Vinyl GABA (4-amino-hex-5-enoic acid), a new selective irreversible inhibitor of GABA-T: effects on brain GABA metabolism in mice.
    J Neurochem. 1977 Nov;29(5):797-802 PMID: 591956
  6. Acetylderivatives as intermediates in polyamine catabolism.
    Int J Biochem. 1981;13(3):287-92 PMID: 7215618
  7. The effect of 4-amino hex-5-ynoic acid (gamma-acetylenic GABA, gammma-ethynyl GABA) a catalytic inhibitor of GABA transaminase, on brain GABA metabolism in vivo.
    J Neurochem. 1977 Apr;28(4):717-23 PMID: 894280
  8. Regulatory interrelations between GABA and polyamines. I. Brain GABA levels and polyamine metabolism.
    Neurochem Res. 1979 Aug;4(4):425-35 PMID: 481678
  9. The effect of DL-allylglycine on polyamine and GABA metabolism in mouse brain.
    J Neurochem. 1979 May;32(5):1401-8 PMID: 438812
  10. Distribution of putreanine in organs of rats and rabbits.
    J Neurochem. 1971 Dec;18(12):2547-8 PMID: 5135910
  11. Interconversion, catabolism and elimination of the polyamines.
    Med Biol. 1981 Dec;59(5-6):334-46 PMID: 7040832
  12. The influence of catabolic reactions on polyamine excretion.
    Biochem J. 1985 Jan 1;225(1):219-26 PMID: 3977824
  13. Diamine oxidase in the brain of vertebrates.
    J Neurochem. 1963 Mar;10:183-6 PMID: 14017033
  14. High-performance liquid chromatographic procedure for the simultaneous determination of the natural polyamines and their monoacetyl derivatives.
    J Chromatogr. 1980 Dec 12;221(2):227-35 PMID: 7217292
  15. On the nonoccurrence of ornithine decarboxylase in nerve endings.
    Neurochem Res. 1980 Jan;5(1):97-100 PMID: 6767991
  16. Studies on ornithine decarboxylase from the liver of thioacetamide-treated rats. Purification and some properties.
    Biochim Biophys Acta. 1972 Sep 19;284(1):285-97 PMID: 5073764
  17. Allylglycine affects acetylation of putrescine and spermidine in mouse brain.
    Neuropharmacology. 1983 Oct;22(10):1237-9 PMID: 6646356
  18. Enzyme-activated irreversible inhibitors of L-ornithine:2-oxoacid aminotransferase. Demonstration of mechanistic features of the inhibition of ornithine aminotransferase by 4-aminohex-5-ynoic acid and gabaculine and correlation with in vivo activity.
    J Biol Chem. 1978 Oct 25;253(20):7431-9 PMID: 701263
  19. Polyamine oxidase in rat tissues.
    Biochim Biophys Acta. 1980 Oct;615(2):480-8 PMID: 7417459
  20. On the role of S-adenosyl-L-methionine in the biosynthesis of spermidine by rat prostate.
    J Biol Chem. 1969 Feb 25;244(4):682-93 PMID: 4889860
  21. Formation of acetylpolyamines in the liver of fasting animals.
    Int J Biochem. 1981;13(12):1205-14 PMID: 6172297
  22. The determination of N1-acetylspermine in mouse liver.
    Biochim Biophys Acta. 1981 Aug 5;676(1):1-7 PMID: 7260107
Article Info
Journal
Neurochemical research
Abbr.
Neurochem Res
ISSN
0364-3190
Published
1985-04-00
Pages
529-44
Language
English
Region
United States
NLM ID
7613461
Subset
IM
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