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 Littman, E.
Right arrow Articles by Wedeen, R. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Littman, E.
Right arrow Articles by Wedeen, R. P.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*DIMERCAPROL
*MERCURY COMPOUNDS
*MERCURY, ELEMENTAL
Journal of Pharmacology And Experimental Therapeutics, Vol. 152, Issue 1, 130-138, 1966
Copyright © 1966 by American Society for Pharmacology and Experimental Therapeutics


THE RELATIONSHIP OF THE INTRARENAL DISTRIBUTION OF Hg203-CHLORMERODRIN TO THE DIURETIC EFFECT

Edward Littman 1, Marvin H. Goldstein 1, Leonard Kasen 1, Marvin F. Levitt 1, and Richard P. Wedeen 1

1 Division of Renal Diseases, Department of Medicine and the Andre Meyer Department of Physics, The Mount Sinai Hospital, New York, New York

Autoradiography was employed to examine the relationship between the intrarenal distribution of Hg203-chlormerodrin and the diuretic effect. Experiments were performed in dogs undergoing mercurial diuresis induced during metabolic acidosis and during inhibition of mercurial diuresis by metabolic alkalosis, dithiopropanol and p-chloromercuribenzoic acid. No consistent pattern of intrarenal Hg203 distribution or total renal mercury content could be correlated with the diuretic response It was demonstrated that the presence of maximum mercury concentration at a proximal tubular site does not establish that segment as the locus of diuretic activity. In addition, autoradiographs of human kidney sections revealed a pattern of Hg203 distribution similar to that found in acidotic dogs. It appears that the tubular binding of chlormerodrin need not be solely determined by factors involved in the production of the mercurial diuresis and may be more closely related to tubular secretion than to the diuretic effect.

Accepted on November 9, 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.