Literature DB >> 6260419

Three new long-acting converting-enzyme inhibitors: relationship between plasma converting-enzyme activity and response to angiotensin I.

J Biollaz, M Burnier, G A Turini, D B Brunner, M Porchet, H J Gomez, K H Jones, F Ferber, W B Abrams, H Gavras, H R Brunner.   

Abstract

Three new angiotensin converting-enzyme inhibitors were given orally to 20 men in single doses ranging from 1.25 to 40 mg. Two of them induced comparable marked inhibition of both the blood pressure response to exogenous angiotensin I and plasma converting-enzyme activity. Onset of action was relatively slow, but 21 to 24 hr after drug plasma converting-enzyme activity was still clearly reduced. The third was less active. There was a close correlation between blood pressure response on administration of angiotensin I and plasma converting-enzyme activity. There were no adverse effects. These new drugs are interesting because of their long duration of action. The measurement of plasma converting-enzyme activity seems useful for monitoring efficacy of converting-enzyme blockade and compliance to therapy.

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Year:  1981        PMID: 6260419     DOI: 10.1038/clpt.1981.92

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  40 in total

1.  Blood pressure response to conventional and low-dose enalapril in chronic renal failure.

Authors:  Thomas Elung-Jensen; Jens Heisterberg; Anne-Lise Kamper; Jesper Sonne; Svend Strandgaard
Journal:  Br J Clin Pharmacol       Date:  2003-02       Impact factor: 4.335

2.  Low-dose enalapril in severe chronic heart failure.

Authors:  C G Brilla; B Krämer; H M Hoffmeister; W Müller-Schauenburg; T Risler; L Seipel
Journal:  Cardiovasc Drugs Ther       Date:  1989-04       Impact factor: 3.727

Review 3.  The chemistry of enalapril.

Authors:  A A Patchett
Journal:  Br J Clin Pharmacol       Date:  1984       Impact factor: 4.335

4.  Evaluation of the angiotensin challenge methodology for assessing the pharmacodynamic profile of antihypertensive drugs acting on the renin-angiotensin system.

Authors:  C Buchwalder-Csajka; T Buclin; H R Brunner; J Biollaz
Journal:  Br J Clin Pharmacol       Date:  1999-10       Impact factor: 4.335

5.  [Reproducibility of acute captopril-induced renal insufficiency with enalapril].

Authors:  W Cremer
Journal:  Klin Wochenschr       Date:  1984-01-02

6.  A potent converting enzyme inhibitor CGS 13928C. Drug profile in normal volunteers.

Authors:  M D Schaller; D B Brunner; J Nussberger; G A Turini; S B Sen; D Chen; B Waeber; H R Brunner
Journal:  Eur J Clin Pharmacol       Date:  1984       Impact factor: 2.953

7.  Enalapril (MK421) and its lysine analogue (MK521): a comparison of acute and chronic effects on blood pressure, renin-angiotensin system and sodium excretion in normal man.

Authors:  G P Hodsman; J R Zabludowski; C Zoccali; R Fraser; J J Morton; G D Murray; J I Robertson
Journal:  Br J Clin Pharmacol       Date:  1984-03       Impact factor: 4.335

8.  A comparison of the effects of captopril and enalapril on skin responses to intradermal bradykinin and skin blood flow in the human forearm.

Authors:  T C Li Kam Wa; E D Cooke; P Turner
Journal:  Br J Clin Pharmacol       Date:  1993-01       Impact factor: 4.335

9.  RHC 3659: a new orally active angiotensin converting enzyme inhibitor in normal volunteers.

Authors:  M Burnier; G A Turini; H R Brunner; M Porchet; D Kruithof; R A Vukovich; H Gavras
Journal:  Br J Clin Pharmacol       Date:  1981-12       Impact factor: 4.335

10.  Pharmacodynamics of converting enzyme inhibition: the cardiovascular, endocrine and autonomic effects of MK421 (enalapril) and MK521.

Authors:  J A Millar; F H Derkx; K McLean; J L Reid
Journal:  Br J Clin Pharmacol       Date:  1982-09       Impact factor: 4.335

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