Literature DB >> 2065821

On the degradation and elimination of spermine by the vertebrate organism.

S Sarhan1, V Quemener, J P Moulinoux, B Knödgen, N Seiler.   

Abstract

1. Treatment of mice and rats with the polyamine oxidase inhibitor N1,N4-bis-(2,3-butadienyl)-1,4-butanediamine (MDL 72527) causes a gradual accumulation of spermine in the circulation and a decrease of spermidine concentration. 2. Spermine is mainly localized in the red blood cells. 3. Co-administration of 2-(difluoromethyl)ornithine and MDL 72527 enhances considerably the rate and extent of spermine accumulation in the circulation. 4. It is assumed that the increased rate of spermine accumulation by the two drugs is due to the enhancement of cell death, i.e. spermine accumulation is the result of its release into the circulation from dying cells, not due to physiological release. 5. After discontinuation of polyamine oxidase inhibition spermine appears to be gradually transformed into spermidine by red blood cell polyamine oxidase, obviously without transformation into N1-acetylspermine.

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Year:  1991        PMID: 2065821     DOI: 10.1016/0020-711x(87)90057-7

Source DB:  PubMed          Journal:  Int J Biochem        ISSN: 0020-711X


  3 in total

1.  Identification and characterization of a novel flavin-containing spermine oxidase of mammalian cell origin.

Authors:  Slavoljub Vujcic; Paula Diegelman; Cyrus J Bacchi; Debora L Kramer; Carl W Porter
Journal:  Biochem J       Date:  2002-11-01       Impact factor: 3.857

Review 2.  Polyamines in brain tumor therapy.

Authors:  E S Redgate; S Boggs; A Grudziak; M Deutsch
Journal:  J Neurooncol       Date:  1995       Impact factor: 4.130

3.  The role of hypusine depletion in cytostasis induced by S-adenosyl-L-methionine decarboxylase inhibition: new evidence provided by 1-methylspermidine and 1,12-dimethylspermine.

Authors:  T L Byers; J R Lakanen; J K Coward; A E Pegg
Journal:  Biochem J       Date:  1994-10-15       Impact factor: 3.857

  3 in total

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