Literature DB >> 8842505

Acute hemodynamic effects and preload-dependent cardiovascular profile of the partial phosphodiesterase inhibitor nanterinone in patients with mild to moderate heart failure.

W J Remme1, M van der Ent, G L Bartels, D van Schelven, D C van Hoogenhuyze, X H Krauss, H A Kruijssen, C J Storm.   

Abstract

Nanterinone (UK-61,260) is a novel positive inotropic and balanced-type vasodilating drug, only partially based on phosphodiesterase III inhibition. Preliminary data from controlled studies suggest satisfactory long-term efficacy and safety. As its acute hemodynamic effects in humans are unknown, an oral dose of 2 mg nanterinone was studied in 14 patients with heart failure (NYHA class II-III) on chronic diuretic and angiotensin-converting enzyme (ACE) inhibitor treatment. Before the study, patients were on a 2 g salt-balanced diet, and they received their last medication 16 hours before each study day. Hemodynamic measurements were carried out before and 0.5, 1, 1.5, 2, 2.5, 3, 4, 8, 12, and 24 hours after administration of the study drug. All patients received placebo and nanterinone on 2 consecutive days. Following nanterinone, systemic vascular resistance decreased immediately from 1699 +/- 82 (mean +/- SEM) at baseline to 1368 +/- 80 at 1 hour. Changes persisted for 12 hours. Concomitantly, there was an immediate and significant fall in pulmonary wedge pressure to 38% of baseline at 1.5 hours, together with a 20% reduction in pulmonary artery pressure. Heart rate remained unchanged and arterial pressures showed only a short, significant decrease. Cardiac index rose significantly from 2.28 +/- 0.15 at baseline to a highest value of 2.65 +/- 0.14 1/min/m2 at 1 hour. Changes persisted for 3 hours. Placebo had no effect on these variables. As, in view of its potential venodilating properties, hemodynamic improvement by nanterinone may depend on pre-existing left ventricular filling pressure, patients were subsequently grouped according to baseline pulmonary wedge pressure of > 12 mmHg (H-PCWP) and < or = 12 mmHg (L-PCWP). Cardiac index improved by 26% in H-PCWP and by 17% in L-PCWP (NS). In contrast, PCWP fell more markedly in H-PWCP than in L-PCWP (40% and 23%, respectively, p < 0.05). Thus, oral nanterinone results in a significant acute hemodynamic improvement and is well tolerated. Although changes in left ventricular filling pressure are more pronounced in patients with elevated pre-existing PCWP, cardiac pump function improves equally in patients with normal or low left ventricular filling pressure at baseline.

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Year:  1996        PMID: 8842505     DOI: 10.1007/bf00823591

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


  13 in total

1.  "Inodilators".

Authors:  L H Opie
Journal:  Lancet       Date:  1986-06-07       Impact factor: 79.321

2.  The acute hemodynamic effects of a new agent, MDL 17,043, in the treatment of congestive heart failure.

Authors:  B F Uretsky; T Generalovich; P S Reddy; R B Spangenberg; W P Follansbee
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3.  2(1H)-quinolinones with cardiac stimulant activity. 2. Synthesis and biological activities of 6-(N-linked, five-membered heteroaryl) derivatives.

Authors:  C T Alabaster; A S Bell; S F Campbell; P Ellis; C G Henderson; D S Morris; D A Roberts; K S Ruddock; G M Samuels; M H Stefaniak
Journal:  J Med Chem       Date:  1989-03       Impact factor: 7.446

4.  Positive inotropic and vasodilator actions of milrinone in patients with severe congestive heart failure. Dose-response relationships and comparison to nitroprusside.

Authors:  B E Jaski; M A Fifer; R F Wright; E Braunwald; W S Colucci
Journal:  J Clin Invest       Date:  1985-02       Impact factor: 14.808

5.  Oral amrinone in refractory congestive heart failure.

Authors:  J Wynne; R F Malacoff; J R Benotti; G D Curfman; W Grossman; B L Holman; T W Smith; E Braunwald
Journal:  Am J Cardiol       Date:  1980-06       Impact factor: 2.778

6.  Intravenous and oral MDL 17043 (a new inotrope-vasodilator agent) in congestive heart failure: hemodynamic and clinical evaluation in 38 patients.

Authors:  D Kereiakes; K Chatterjee; W W Parmley; B Atherton; D Curran; A Kereiakes; R Spangenberg
Journal:  J Am Coll Cardiol       Date:  1984-11       Impact factor: 24.094

7.  Physiologic assessment of the inotropic, vasodilator and afterload reducing effects of milrinone in subjects without cardiac disease.

Authors:  K M Borow; P C Come; A Neumann; D S Baim; E Braunwald; W Grossman
Journal:  Am J Cardiol       Date:  1985-04-15       Impact factor: 2.778

8.  Sustained hemodynamic and clinical effects of a new cardiotonic agent, WIN 47203, in patients with severe congestive heart failure.

Authors:  C S Maskin; L Sinoway; B Chadwick; E H Sonnenblick; T H Le Jemtel
Journal:  Circulation       Date:  1983-05       Impact factor: 29.690

9.  Intracoronary infusion of dobutamine to patients with and without severe congestive heart failure. Dose-response relationships, correlation with circulating catecholamines, and effect of phosphodiesterase inhibition.

Authors:  W S Colucci; A R Denniss; G F Leatherman; R J Quigg; P L Ludmer; J D Marsh; D F Gauthier
Journal:  J Clin Invest       Date:  1988-04       Impact factor: 14.808

Review 10.  Clinical results with oral milrinone in heart failure.

Authors:  R DiBianco
Journal:  Eur Heart J       Date:  1989-08       Impact factor: 29.983

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