JPET xPharm- The Comprehensive Pharmacology Reference

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 Hare, H. G.
Right arrow Articles by Gosselin, R. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hare, H. G.
Right arrow Articles by Gosselin, R. E.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Medline Plus Health Information
*Blood and Blood Disorders
*Dialysis
*Kidney Failure
Hazardous Substances DB
*POTASSIUM
*VASOPRESSIN
Journal of Pharmacology And Experimental Therapeutics, Vol. 145, Issue 1, 122-129, 1964
Copyright © 1964 by American Society for Pharmacology and Experimental Therapeutics


EFFECT OF DRUGS ON PERITONEAL DIALYSIS IN THE DOG

H. G. Hare 1, H. Valtin 1, and R. E. Gosselin 1

1 Departments of Pharmacology and Physiology, Dartmouth Medical School, Hanover, New Hampshire

The rates of migration of potassium and iodide ions during peritoneal dialysis in dogs can be modified by adding drugs and enzymes to the dialysis fluid. Net fluxes of potassium diffusing from blood into the peritoneal cavity and of I131-iodide moving in the opposite direction have been expressed in terms of dialysance. The addition of hyaluronidase and papain caused no significant change in the dialysance of either solute. Vasopressin significantly decreased the values for both potassium and iodide, the fractional decrement being greater for the latter. In contrast, the constants for both ions increased significantly when streptokinase was added to the dialysis fluid. Serotonin also increased the constants for both ions, but significantly so only for potassium.

As a measure of the rate of solute exchange between blood and peritoneal fluid, the dialysance might be altered by any drug that influences splanchnic blood flow or the permeability of the interposed membranes, or both. The present results suggest that vasopressin in dialysis fluid decreased splanchnic blood flow and also altered the permeability of the dialyzing membranes. The results with streptokinase and serotonin are best explained by increases in permeability of one or more diffusion barriers between peritoneal cavity and blood.

Accepted on February 19, 1964







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

Copyright © 1964 by the American Society for Pharmacology and Experimental Therapeutics.