Literature DB >> 6129139

Clinical pharmacology of a new beta-adrenoceptor blocking drug, befunolol. Cross-over comparison with propranolol on repeated administration.

A Ebihara, K Tawara, T Oka, T Ofuji, K Kawahara.   

Abstract

Repeated doses of a new beta-adrenoceptor blocking agent, befunolol, were administered orally to adult male volunteers for a cross-over comparison with propranolol. The beta-adrenoceptor blocking activity of befunolol was greater than that of propranolol when assessed by the percentage reduction in exercise-induced tachycardia. The elimination half-life of drug was significantly prolonged on repeated administration of propranolol, but not of befunolol. The percentage reduction in exercise-induced tachycardia was highly correlated with the log plasma level of each drug. Both drugs produced a significant reduction in pre-exercise systolic and diastolic blood pressure, and significant attenuation of exercise-induced rise in systolic blood pressure.

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Year:  1982        PMID: 6129139     DOI: 10.1007/bf00547552

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  15 in total

1.  Simultaneous determination of befunolol, a beta-blocking agent, and its metabolite in human plasma by gas chromatography with electron-caputre detection.

Authors:  K Kawahara; T Ofuji
Journal:  J Chromatogr       Date:  1979-01-11

2.  Disposition of propranolol. VI. Independent variation in steady-state circulating drug concentrations and half-life as a result of plasma drug binding in man.

Authors:  G H Evans; D G Shand
Journal:  Clin Pharmacol Ther       Date:  1973 Jul-Aug       Impact factor: 6.875

3.  Disposition of propranolol. V. Drug accumulation and steady-state concentrations during chronic oral administration in man.

Authors:  G H Evans; D G Shand
Journal:  Clin Pharmacol Ther       Date:  1973 Jul-Aug       Impact factor: 6.875

4.  Plasma propranolol levels in adults with observations in four children.

Authors:  D G Shand; E M Nuckolls; J A Oates
Journal:  Clin Pharmacol Ther       Date:  1970 Jan-Feb       Impact factor: 6.875

5.  [Identification of urinary metabolites of befunolol in dog and man principally by mass spectrometry (author's transl)].

Authors:  M Tohno; K Kimura; M Nagahara; Y Sakai; T Ofuji; T Nadai
Journal:  Yakugaku Zasshi       Date:  1979-09       Impact factor: 0.302

6.  [The beta-adrenergic blocking and antiarrhythmic activities of metabolites of befunolol hydrochloride (author's transl)].

Authors:  S Masumoto; H Inoue; Y Maruyama
Journal:  Nihon Yakurigaku Zasshi       Date:  1979-07

7.  One and three doses of propranolol a day in hypertension.

Authors:  G van den Brink; P Boer; P van Asten; E J Dorhout Mees; G G Geyskes
Journal:  Clin Pharmacol Ther       Date:  1980-01       Impact factor: 6.875

8.  Pharmacology of 4-hydroxypropranolol, a metabolite of propranolol.

Authors:  J D Fitzgerald; S R O'Donnell
Journal:  Br J Pharmacol       Date:  1971-09       Impact factor: 8.739

9.  Treatment of hypertension with propranolol.

Authors:  B N Prichard; P M Gillam
Journal:  Br Med J       Date:  1969-01-04

10.  4-Hydroxypropranolol and its glucuronide after single and long-term doses of propranolol.

Authors:  T Walle; E C Conradi; U K Walle; T C Fagan; T E Gaffney
Journal:  Clin Pharmacol Ther       Date:  1980-01       Impact factor: 6.875

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