Literature DB >> 6883416

Influence of chlorpromazine on lysosomal alterations during myocardial ischaemia.

K R Chien, J S Crie, R S Decker, K Wildenthal.   

Abstract

Ligation of the circumflex artery of anaesthetised, open-chest rabbits caused a progressive increase in nonsedimentable cathepsin D activity in severely ischaemic myocardium and an anatomical redistribution of the enzyme from lysosomes into the cytosol, along with progressive ultrastructural signs of cellular damage and necrosis. Chlorpromazine pretreatment (15 mg X kg-1 intravenously) reduced the increase in nonsedimentable cathepsin D activity slightly, but no appreciable protective effect on the anatomical redistribution of the enzyme or the development of ultrastructural signs of necrosis could be detected. It is concluded that in this experimental model of myocardial infarction, high concentrations of chlorpromazine have a mild stabilising action on lysosomes, but the drug has minimal if any effect in protecting the heart from ischaemic damage.

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Year:  1983        PMID: 6883416     DOI: 10.1093/cvr/17.7.407

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN: 0008-6363            Impact factor:   10.787


  2 in total

1.  Inhibition of the release of arachidonic acid prevents the development of sarcolemmal membrane defects in cultured rat myocardial cells during adenosine triphosphate depletion.

Authors:  A Sen; J C Miller; R Reynolds; J T Willerson; L M Buja; K R Chien
Journal:  J Clin Invest       Date:  1988-10       Impact factor: 14.808

2.  Release of arachidonate from membrane phospholipids in cultured neonatal rat myocardial cells during adenosine triphosphate depletion. Correlation with the progression of cell injury.

Authors:  K R Chien; A Sen; R Reynolds; A Chang; Y Kim; M D Gunn; L M Buja; J T Willerson
Journal:  J Clin Invest       Date:  1985-06       Impact factor: 14.808

  2 in total

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