Antihypertensive therapy with MK 421: angiotensin II--renin relationships to evaluate efficacy of converting enzyme blockade

J Cardiovasc Pharmacol. 1982 Nov-Dec;4(6):966-72.

Abstract

Nineteen hypertensive patients were treated with increasing doses of the new angiotensin-converting enzyme inhibitor MK 421. Twenty milligrams orally reduced blood pressure from 180/112 +/- 6.8/3.6 (mean +/- SEM) to 160/100 +/- 6.5/3.3 mm Hg (p less than 0.005) while heart rate increased from 75 +/- 2 to 87 +/- 3 beats/min (p less than 0.005). Plasma converting enzyme activity was still markedly reduced 24 h following 2.5, 5, 10, or 20 mg MK 421 p.o. (p less than 0.001). In nine patients treated with 20 mg b.i.d. for up to 10 months, blood pressure was controlled, with the association of hydrochlorothiazide 50 mg q.d. in five. However, 12 to 16 h following the preceding drug administration, plasma angiotensin II and aldosterone were back to base-line levels. Analysis of plasma angiotensin II-renin relationships strongly suggests that converting enzyme blockade is not complete even 4 h after 20 mg MK 421 and starts to wear off already at 12 h. Thus, MK 421 20 mg taken orally twice daily, effectively reduces blood pressure, but does not constantly suppress plasma angiotensin II and aldosterone. Whether its long duration of action makes once daily administration possible has not yet been established.

MeSH terms

  • Adult
  • Aged
  • Aldosterone / blood
  • Angiotensin II / blood*
  • Angiotensin-Converting Enzyme Inhibitors*
  • Blood Pressure / drug effects
  • Dipeptides / pharmacology*
  • Dose-Response Relationship, Drug
  • Drug Therapy, Combination
  • Enalapril
  • Female
  • Heart Rate / drug effects
  • Humans
  • Hydrochlorothiazide / pharmacology
  • Hypertension / drug therapy*
  • Male
  • Middle Aged
  • Renin / blood*
  • Renin-Angiotensin System / drug effects

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Dipeptides
  • Hydrochlorothiazide
  • Angiotensin II
  • Aldosterone
  • Enalapril
  • Renin