Literature DB >> 2930543

Spermine antagonizes the binding of adriamycin to the inner membrane of heart mitochondria.

G Solaini1.   

Abstract

The biologically active polyamine, spermine, has been found to function as a cationic antagonist of adriamycin binding to ox heart submitochondrial particles. This effect is specifically shown by spermine since other cations tested in the same conditions, can antagonize the binding only to a very low extent. Analysis of the adriamycin binding data in the presence of spermine indicate that the polyamine can greatly reduce the total number of binding sites for the anthracycline in submitochondrial particles and it can increase the apparent dissociation constant, whilst it leaves unchanged the degree of cooperativity of the binding. These results provide evidence on previously unexplored effects of spermine, suggesting that this polyamine might be examined as a possible in vivo antagonist of the adriamycin binding to mitochondria.

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Year:  1989        PMID: 2930543     DOI: 10.1016/0006-291x(89)90064-8

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  2 in total

1.  Effect of exogenously applied polyamines on malathion toxicity in the toad Bufo arenarum Hensel.

Authors:  A Venturino; L E Gauna; R M Bergoc; A M Pechen de D'Angelo
Journal:  Arch Environ Contam Toxicol       Date:  1992-01       Impact factor: 2.804

2.  Tuning Receptor Properties of Metal-Amyloid Beta Complexes. Studies on the Interaction between Ni(II)-Aβ5-9 and Phosphates/Nucleotides.

Authors:  Aleksandra Tobolska; Nina E Wezynfeld; Urszula E Wawrzyniak; Wojciech Bal; Wojciech Wróblewski
Journal:  Inorg Chem       Date:  2021-12-08       Impact factor: 5.165

  2 in total

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