Abstract
Changes in tension of spiral strips from dog saphenous, external carotid and basilar arteries were monitored isometrically. Serotonin (5-HT) contracted the 3 arterial preparations in about the same concentration range. Compared with noradrenaline (NA) (100%) the efficacy of 5-HT was about 60% on saphenous, 150% on external carotid and about 500% on basilar arteries. Ergotamine (E) stimulated the 3 vascular preparations in concentrations about 100 times lower than 5-HT. Compared with NA the efficacy of E was about 20% on saphenous, 50% on external carotid and 200% on basilar arteries. Compared with 5-HT (100%) however, E had similar constrictor activities in the 3 arteries. It seemed likely therefore that 5-HT receptors are involved in the vasoconstrictor activity of E. Evidence for this was obtained in experiments in which cyproheptadine (Cy), a 5-HT antagonist, was used. For antagonism of E concentrations of Cy about 6 times higher than those required to inhibit 5-HT were necessary, whereas for antagonism of NA about 500 times higher Cy concentrations were necessary. The results suggest that on canine arterial vascular smooth muscle the constrictor activity of E is mediated mainly through serotoninergic receptor sites.
MeSH Terms
Animals
Arteries/drug effects
Basilar Artery/drug effects
Carotid Artery, External/drug effects
Cerebral Arteries/drug effects
Cyproheptadine/pharmacology
Dogs
Ergotamine/antagonists & inhibitors,pharmacology
Female
In Vitro Techniques
Male
Muscle Contraction/drug effects
Muscle, Smooth/drug effects
Norepinephrine/pharmacology
Serotonin/pharmacology
Serotonin Antagonists
Vasomotor System/drug effects
Chemicals
Serotonin Antagonists
Cyproheptadine
Serotonin
Ergotamine
Norepinephrine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Müller-Schweinitzer E
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20 references, click to expand
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