In vivo pharmacology of SC-51316, a nonpeptidic angiotensin II receptor antagonist

Am J Hypertens. 1993 Jul;6(7 Pt 1):619-25. doi: 10.1093/ajh/6.7.619.

Abstract

The depressor activity of a novel nonpeptidic angiotensin II (AII) receptor antagonist, SC-51316 (2,5-dibutyl-2,4-dihydro-4-[[2-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4 '- yl]-methyl]-3H-1,2,4-triazol-3-one), is described. In anesthetized, ganglion-blocked rats, intravenous administration of SC-51316 inhibited the pressor response to an infusion of AII. To determine antihypertensive efficacy, conscious, spontaneously hypertensive rats were administered SC-51316 (30 mg/kg intragastrically) daily for 5 days. Blood pressure was reduced in a similar manner to that observed with the angiotensin converting enzyme inhibitor enalapril (10 mg/kg intragastrically). SC-51316 had no effect on heart rate. In conscious, sodium-deficient dogs, administration of SC-51316 (30 mg/kg orally) or enalapril (10 mg/kg orally) lowered blood pressure similarly over a 24 h observation period. Thus, SC-51316 antagonizes the activity of AII in vivo and is an orally active, antihypertensive agent.

Publication types

  • Comparative Study

MeSH terms

  • Angiotensin II / antagonists & inhibitors
  • Angiotensin II / physiology
  • Angiotensin Receptor Antagonists*
  • Animals
  • Biphenyl Compounds / pharmacology
  • Biphenyl Compounds / therapeutic use
  • Blood Pressure / drug effects*
  • Depression, Chemical
  • Dogs
  • Dose-Response Relationship, Drug
  • Enalapril / pharmacology
  • Enalapril / therapeutic use
  • Hypertension / drug therapy*
  • Imidazoles / pharmacology
  • Imidazoles / therapeutic use
  • Losartan
  • Male
  • Rats
  • Rats, Inbred SHR
  • Rats, Sprague-Dawley
  • Tetrazoles / pharmacology*
  • Tetrazoles / therapeutic use
  • Triazoles / pharmacology*
  • Triazoles / therapeutic use

Substances

  • Angiotensin Receptor Antagonists
  • Biphenyl Compounds
  • Imidazoles
  • Tetrazoles
  • Triazoles
  • Angiotensin II
  • SC 51316
  • Enalapril
  • Losartan