JPET Celsis microsomes equal better data

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ogawa, K.
Right arrow Articles by Bing, R. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ogawa, K.
Right arrow Articles by Bing, R. J.
Journal of Pharmacology And Experimental Therapeutics, Vol. 155, Issue 3, 449-455, 1967
Copyright © 1967 by American Society for Pharmacology and Experimental Therapeutics


NITROGLYCERIN (GLYCERYL TRINITRATE) AS A MONOAMINE OXIDASE INHIBITOR

Kouichi Ogawa 1, Sigmundur Gudbjarnason 1, and Richard J. Bing 1

1 Department of Medicine, Wayne State University School of Medicine, Detroit, Michigan

The biochemical effect of nitroglycerin on myocardial monoamine oxidase (MAO) activity was studied in vivo and in vitro. Nitroglycerin administered in vivo inhibited significantly the MAO activity of rat heart mitochondria with tyramine as substrate. Nitroglycerin also inhibited MAO activity of rat heart mitochondria in vitro with both tyramine and tryptamine as substrates. The mechanism of the inhibition of the MAO activity by nitroglycerin was studied in vitro on a solubilized and partially purified mitochondrial monoamine oxidase. The effect of nitroglycerin on the enzyme kinetics of MAO indicated that the drug acts as competitive inhibitor of MAO. A significant inhibition of rat liver and brain MAO activity was also observed in the presence of nitroglycerin. The effect of nitroglycerin on MAO activity was compared to that of other organic nitrates, but no correlation was observed between the number of nitrate groups per molecule and the molar inhibitory action.

Submitted on May 31, 1966
Accepted on September 20, 1966







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1967 by the American Society for Pharmacology and Experimental Therapeutics.