Document Detail


Pharmacological and therapeutic properties of an ideal beta-blocker.
MedLine Citation:
PMID:  2906020     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
With hindsight it is now possible to define some of the additional pharmacological characteristics which enhance the pharmacodynamic and therapeutic efficacy of a drug whose primary purpose is to antagonize competitively sympathetic stimulation of the heart. The ideal pharmacokinetic profile for a beta-blocker includes ready and unimpeded absorption; a predominantly hydrophilic distribution; a relatively long duration of pharmacological activity and alternative routes of elimination. The ideal pharmacodynamic activity of such a drug involves a number of factors, including the essential element of beta 1-adrenoceptor selectivity. In addition, moderate beta 2-adrenoceptor agonist activity and mild stimulation of myocardial contractibility afford enhanced haemodynamic efficacy. The intrinsic ability to relax vascular and bronchial smooth muscle are also highly desirable ancillary pharmacodynamic properties. From the therapeutic aspect, a drug administered with the primary objective of reducing myocardial ischaemia in patients with a coronary heart disease, or of lowering blood pressure in patients with hypertension, should not only prove effective in clinical practice, but should also be shown to have beneficial haemodynamic properties and a minimum of undesirable pharmacological effects. The unique pharmacological profile of celiprolol appears to allow fulfillment of many of these desirable objectives.
Authors:
S H Taylor
Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  The Journal of international medical research     Volume:  16 Suppl 1     ISSN:  0300-0605     ISO Abbreviation:  J. Int. Med. Res.     Publication Date:  1988  
Date Detail:
Created Date:  1989-03-23     Completed Date:  1989-03-23     Revised Date:  2005-11-16    
Medline Journal Info:
Nlm Unique ID:  0346411     Medline TA:  J Int Med Res     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  8A-16A     Citation Subset:  IM    
Affiliation:
Department of Medical Cardiology, General Infirmary, Leeds, UK.
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MeSH Terms
Descriptor/Qualifier:
Adrenergic beta-Antagonists / pharmacokinetics,  pharmacology*,  therapeutic use
Animals
Blood Pressure / drug effects
Heart / drug effects
Humans
Chemical
Reg. No./Substance:
0/Adrenergic beta-Antagonists

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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