Literature DB >> 1350480

Pharmacological profile of beta-adrenoceptor blockers with vasodilating properties, especially carvedilol--rationale for clinical use.

G Sponer1, W Bartsch, K Strein.   

Abstract

The rationale for the combined use of beta-adrenoceptor antagonists and vasodilators is to improve the efficacy of the antihypertensive therapy and to reduce the incidence of side effects. If suitable coagents are selected and used at appropriate doses, the disadvantages of each separate component (compromised blood flow to individual organs, increase in total peripheral resistance, unfavorable lipid profile for beta-blockers; stimulation of counter-regulatory mechanisms, retention of water and electrolytes for vasodilators) can be balanced. In addition, the favorable effects of each (reduction in cardiovascular morbidity and mortality for beta-blockers, and favorable hemodynamic profile for vasodilators) may be used to advantage. Such a treatment rationale can be accomplished by a free combination or by using a dual-acting drug. From the practical point of view, the latter may be preferable. The basic requirement for such a drug is that the two effects are evoked in the same dose range. Carvedilol is a dual-acting drug designed to produce beta-blockade and vasodilation in the same dose range. The vasodilation is mediated predominantly by specific alpha 1-adrenoceptor blockade; at markedly higher concentrations additional vasodilating actions can be observed. These effects resemble those of Ca(2+)-antagonistic properties. However, they do not contribute to the acute blood-pressure-lowering activity, but may be responsible for the increased blood flow to some organs. At beta-blocking doses, carvedilol reduces the total peripheral resistance, and blood flow to the kidneys is preserved. Cardioprotection has been demonstrated in a variety of experimental investigations.

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Year:  1992        PMID: 1350480     DOI: 10.1007/bf00207607

Source DB:  PubMed          Journal:  Clin Investig        ISSN: 0941-0198


  28 in total

1.  Long-term reduction of peripheral resistance with celiprolol and effects on left ventricular mass.

Authors:  B Trimarco; G Lembo; N DeLuca; B Ricciardelli; G Rosiello; M Volpe; G Orofino; M Condorelli
Journal:  J Int Med Res       Date:  1988       Impact factor: 1.671

2.  In vitro pharmacologic profile of the novel beta-adrenoceptor antagonist and vasodilator, carvedilol.

Authors:  A J Nichols; A C Sulpizio; D J Ashton; J P Hieble; R R Ruffolo
Journal:  Pharmacology       Date:  1989       Impact factor: 2.547

3.  The interaction of the enantiomers of carvedilol with alpha 1- and beta 1-adrenoceptors.

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Journal:  Chirality       Date:  1989       Impact factor: 2.437

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Authors:  S Yusuf; R Peto; J Lewis; R Collins; P Sleight
Journal:  Prog Cardiovasc Dis       Date:  1985 Mar-Apr       Impact factor: 8.194

5.  Celiprolol: pharmacokinetics and duration of pharmacodynamic activity.

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Journal:  Herz       Date:  1978-08       Impact factor: 1.443

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Authors:  H Pittner
Journal:  Wien Klin Wochenschr Suppl       Date:  1985

Review 8.  Pharmacology of combined alpha-beta-blockade. II. Haemodynamic effects of labetalol.

Authors:  P Lund-Johansen
Journal:  Drugs       Date:  1984       Impact factor: 9.546

9.  Cardiovascular effects of bevantolol, a selective beta 1-adrenoceptor antagonist with a novel pharmacological profile.

Authors:  I D Dukes; E M Vaughan Williams
Journal:  Br J Pharmacol       Date:  1985-02       Impact factor: 8.739

10.  Pharmacological characteristics of the stereoisomers of carvedilol.

Authors:  W Bartsch; G Sponer; K Strein; B Müller-Beckmann; L Kling; E Böhm; U Martin; H O Borbe
Journal:  Eur J Clin Pharmacol       Date:  1990       Impact factor: 2.953

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  1 in total

Review 1.  An overview of the pharmacodynamic properties and therapeutic potential of combined alpha- and beta-adrenoceptor antagonists.

Authors:  P A van Zwieten
Journal:  Drugs       Date:  1993-04       Impact factor: 9.546

  1 in total

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