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Hypertensinogenic potencies of aldosterone and deoxycorticosterone in the rat.

Abstract
Hypertensinogenic potency and other effects of acetate salts of aldosterone (ALA) and deoxycorticosterone (DOCA) were evaluated in 50-day-old mononephrectomized and saline-drinking Sprague-Dawley CD male rats. The steroids were administered by continuous subcutaneous infusion in a dose of 100 microgram/24 hrs by means of Alzet osmotic minipumps implanted subcutaneously. Within 3 weeks of steroid treatment, systolic blood pressure, measured in the tail of conscious animals by a photoelectric cell method at 27 degrees C environmental temperature, increased significantly in ALA rats as compared to that in DOCA rats, which was not different from controls. ALA rats exhibited marked polydipsia, decreased body weight, hypernatremia, hypokalemia, cardiomegaly, and kidney enlargement, whereas DOCA rats exhibited only cardiomegaly when compared with controls. The degree of cardiomegaly in ALA and DOCA rats was statistically much greater than the differences in their respective blood pressure levels when compared to controls. Under the conditions of this study, it is concluded that: 1) the hypertensinogenic potency of ALA is greater than that of DOCA; 2) ALA and DOCA may induce cardiomegaly, independent of their effect on blood pressure; 3) Alzet osmotic minipumps are effective tools for the administration of steroids by continuous infusion.
AuthorsP Komanicky, J C Melby
JournalHypertension (Dallas, Tex. : 1979) (Hypertension) 1982 Jan-Feb Vol. 4 Issue 1 Pg. 140-5 ISSN: 0194-911X [Print] United States
PMID7061121 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Desoxycorticosterone
  • Aldosterone
  • Sodium
  • Potassium
Topics
  • Aldosterone (pharmacology)
  • Animals
  • Blood Pressure (drug effects)
  • Body Weight (drug effects)
  • Desoxycorticosterone (pharmacology)
  • Hypertension (chemically induced)
  • Male
  • Potassium (metabolism)
  • Rats
  • Rats, Inbred Strains
  • Sodium (metabolism)

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