Literature DB >> 8573547

Renin inhibition.

H D Kleinert1.   

Abstract

Modification of the renin-angiotensin-aldosterone system by renin inhibitors may be an alternative to angiotensin-converting enzyme inhibitors in the treatment of cardiovascular disease. The development of clinically useful renin inhibitors has been hampered by a variety of pharmacologic problems, most notably the poor oral bioavailability of these peptide-related compounds. Peptidomimetic renin inhibitors that have been stabilized to enzymatic degradation in conjunction with optimizing physical characteristics amenable to intestinal absorption offer the greatest promise to date. Studies in animal models demonstrate that renin inhibitors are capable of reducing both systolic and diastolic blood pressures without causing reflex tachycardia. The response appears to be sustained with chronic administration. The beneficial cardiovascular effects of these compounds have been confirmed in the few studies conducted in patients with hypertension and in those with congestive heart failure. Further development of renin inhibitors is warranted.

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Year:  1995        PMID: 8573547     DOI: 10.1007/bf00878547

Source DB:  PubMed          Journal:  Cardiovasc Drugs Ther        ISSN: 0920-3206            Impact factor:   3.727


  69 in total

1.  Hepatic extraction of renin: quantitation and characterization in the isolated perfused rat liver.

Authors:  J A Keiser; J C Romero; L J Kost; N F LaRusso
Journal:  Hepatology       Date:  1987 Nov-Dec       Impact factor: 17.425

Review 2.  New possibilities for intracellular renin and inactive renin now that the structure of the human renin gene has been elucidated.

Authors:  B J Morris
Journal:  Clin Sci (Lond)       Date:  1986-10       Impact factor: 6.124

3.  The amino terminal amino acid sequence of human angiotensinogen.

Authors:  D A Tewksbury; R A Dart; J Travis
Journal:  Biochem Biophys Res Commun       Date:  1981-04-30       Impact factor: 3.575

4.  H-77: a potent new renin inhibitor. In vitro and in vivo studies.

Authors:  M Szelke; B J Leckie; M Tree; A Brown; J Grant; A Hallett; M Hughes; D M Jones; A F Lever
Journal:  Hypertension       Date:  1982 May-Jun       Impact factor: 10.190

5.  Comparative hemodynamic effects of MK-422, a converting enzyme inhibitor, and a renin inhibitor in dogs with acute left ventricular failure.

Authors:  C S Sweet; C T Ludden; C M Frederick; L R Bush; L G Ribeiro
Journal:  J Cardiovasc Pharmacol       Date:  1984 Nov-Dec       Impact factor: 3.105

6.  Plasma renin activity and ischemic heart disease.

Authors:  T W Meade; J A Cooper; W S Peart
Journal:  N Engl J Med       Date:  1993-08-26       Impact factor: 91.245

Review 7.  Nonparallel effects of renin inhibitor treatment on plasma renin activity and angiotensins I and II in hypertensive subjects. An assay-related artifact.

Authors:  F H Derkx; A H van den Meiracker; W Fischli; P J Admiraal; A J Man in't Veld; P van Brummelen; M A Schalekamp
Journal:  Am J Hypertens       Date:  1991-07       Impact factor: 2.689

8.  Simultaneous modeling of the pharmacokinetic and pharmacodynamic properties of enalkiren (Abbott-64662, a new renin inhibitor). I: Single dose study.

Authors:  S K Gupta; G R Granneman; R S Boger; N K Hollenberg; R R Luther
Journal:  Drug Metab Dispos       Date:  1992 Nov-Dec       Impact factor: 3.922

9.  Effects of chronic infusion of renin inhibitor A-64662 in sodium-depleted monkeys.

Authors:  K M Verburg; H D Kleinert; J R Kadam; M A Chekal; P F Mento; B M Wilkes
Journal:  Hypertension       Date:  1989-03       Impact factor: 10.190

10.  Ro 42-5892 is a potent orally active renin inhibitor in primates.

Authors:  W Fischli; J P Clozel; K el Amrani; W Wostl; W Neidhart; H Stadler; Q Branca
Journal:  Hypertension       Date:  1991-07       Impact factor: 10.190

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  1 in total

Review 1.  Renin inhibitors: cardiovascular drugs of the future?

Authors:  J M Wood; P Close
Journal:  Cardiovasc Drugs Ther       Date:  1996-07       Impact factor: 3.727

  1 in total

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