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 Butler, T. C.
Right arrow Articles by Poole, D. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Butler, T. C.
Right arrow Articles by Poole, D. T.
Journal of Pharmacology And Experimental Therapeutics, Vol. 152, Issue 1, 62-66, 1966
Copyright © 1966 by American Society for Pharmacology and Experimental Therapeutics


EFFECTS OF 5,5-DIMETHYL-2,4-OXAZOLIDINEDIONE (DMO) ON ACID-BASE AND ELECTROLYTE EQUILIBRIA

Thomas C. Butler 1, Yukio Kuroiwa 1, William J. Waddell 1, and Doris T. Poole 1

1 Department of Pharmacology, University of North Carolina School of Medicine, Chapel Hill, North Carolina

5,5-Dimethyl-2,4-oxazolidinedione (DM0), the product of demethylation of trimethadione, when administered to rats in high dosage causes a decrease in plasma bicarbonate and chloride and a decrease in intracellular pH of skeletal muscle. When DMO is given intravenously to dogs, the acute effect is a fall in plasma bicarbonate. When dosage is continued by mouth on a chronic schedule, plasma bicarbonate returns to normal and plasma chloride decreases. In man, DMO causes a decrease in plasma bicarbonate equivalent to the concentration of the DMO anion. There is no effect on plasma chloride. It is suggested that the effectiveness of DMO in petit ma! epilepsy may be attributed to its property of being an unmetabolizable, slowly excreted acid that accumulates in large amounts to produce changes in extracellular and intracellular acid-base equilibria, which in some way influence the incidence of seizures.

Accepted on November 1, 1965







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

Copyright © 1966 by the American Society for Pharmacology and Experimental Therapeutics.