Abstract
1. The beta-adrenoceptor blocking properties of 1-(p-allylphenoxy)-3-isopropylamino-2-propanol hydrochloride (H 64/52) on the cardiovascular and bronchomotor responses to isoprenaline have been determined in the anaesthetized dog.2. H 64/52 selectively blocked the isoprenaline-induced increase in heart rate, contractile force and reduction in airway pressure in the same dose range.3. H 64/52 produced a minimal blockade of vascular beta-adrenoceptors which was apparent only when the isoprenaline-induced fall in diastolic pressure was considered. No significant vascular beta-adrenoceptor blockade with H 64/52 could be shown with the femoral arterial flow or hind-limb perfusion studies.4. These results further support the hypothesis that several different beta-adrenoceptor subtypes exist in the dog. The beta-adrenoceptors subserving cardiac stimulation and bronchodilation appear to be similar and both differ from the beta-adrenoceptor subserving vasodilatation.
MeSH Terms
Adrenergic beta-Antagonists/pharmacology
Airway Resistance/drug effects
Allyl Compounds/pharmacology
Amino Alcohols/administration & dosage,pharmacology
Animals
Blood Pressure/drug effects
Bronchi/drug effects
Dogs
Dose-Response Relationship, Drug
Drug Interactions
Heart/drug effects
Heart Rate/drug effects
In Vitro Techniques
Isoproterenol/administration & dosage,pharmacology
Perfusion
Phenols/pharmacology
Receptors, Adrenergic/drug effects
Vagotomy
Vagus Nerve/physiology
Chemicals
Adrenergic beta-Antagonists
Allyl Compounds
Amino Alcohols
Phenols
Receptors, Adrenergic
Isoproterenol
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Levy B
References (13)
13 references, click to expand
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