JPET

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 BERNDT, W. O.
Right arrow Articles by GROTE, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by BERNDT, W. O.
Right arrow Articles by GROTE, D.
Journal of Pharmacology And Experimental Therapeutics, Vol. 164, Issue 1, 223-231, 1968
Copyright © 1968 by American Society for Pharmacology and Experimental Therapeutics


THE ACCUMULATION OF C14-DINITROPHENOL BY SLICES OF RABBIT KIDNEY CORTEX

W. O. BERNDT 1 and DACE GROTE 1

1 Department of Pharmacology and Toxicology, Dartmouth Medical School, Hanover, New Hampshire

Standard tissue-slice techniques have been employed to examine the uptake of the metabolic inhibitor, 2, 4-dinitrophenol (DNP) by rabbit renal cortex. For this study the uptake of C14-dinitrophenol (C14-DNP) was monitored. No metabolism of the C14-DNP by slices of renal cortex was detected with paper chromatography. Steady-state slice/medium ratios of 10 to 15 were attained in 40 to 60 mm. Various metabolic inhibitors (e.g., sodium cyanide, iodoacetamide, p-chloromercuribenzoate) reduced the accumulation significantly. Although some metabolic intermediates (e.g., acetate, glucose) failed to influence the C14 accumulation, most reduced the uptake. Other organic acids known to be transported by the renal organic anion transport system also inhibited the C14-DNP uptake (e.g., octanoate, decanoate, p-aminohippurate). Various organic bases were tested but did not influence DNP accumulation. Furthermore, alterations in the potassium ion concentration of the bathing solution did not affect DNP uptake. Also, no pH optimum was found. It was concluded that the accumulation of C14-DNP occurred by two processes: 1) active uptake by the renal organic acid transport process, and 2) a nonspecific binding or partitioning.

Submitted on May 15, 1968
Accepted on July 5, 1968







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

Copyright © 1968 by the American Society for Pharmacology and Experimental Therapeutics.