Cardiac postjunctional supersensitivity to β-agonists after chronic chemical sympathectomy with 6-hydroxydopamine

The sensitivity to sympathomimetic amines of isolated atria removed from sham-injected and 6-hydroxydopamine-treated (6-OHDA) guinea-pigs was examined in the presence of an extraneuronal uptake blocker and an alpha-adrenoceptor antagonist. Three weeks of pretreatment with 6-OHDA resulted in leftward...

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Veröffentlicht in:Naunyn-Schmiedeberg's archives of pharmacology 1985-04, Vol.329 (2), p.162-166
Hauptverfasser: CHESS-WILLIAMS, R. G, GRASSBY, P. F, CULLING, W, PENNY, W, BROADLEY, K. J, SHERIDAN, D. J
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container_title Naunyn-Schmiedeberg's archives of pharmacology
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creator CHESS-WILLIAMS, R. G
GRASSBY, P. F
CULLING, W
PENNY, W
BROADLEY, K. J
SHERIDAN, D. J
description The sensitivity to sympathomimetic amines of isolated atria removed from sham-injected and 6-hydroxydopamine-treated (6-OHDA) guinea-pigs was examined in the presence of an extraneuronal uptake blocker and an alpha-adrenoceptor antagonist. Three weeks of pretreatment with 6-OHDA resulted in leftwards shifts of the dose-response curves for the positive chronotropic and inotropic responses of right and left atria to isoprenaline. The responses to the partial agonist salbutamol were also potentiated after 6-OHDA pretreatment, revealed as an increase in the maximum response relative to isoprenaline. The supersensitivity was post-synaptic in origin and independent of changes in disposition or metabolism, since it was observed with agonists immune to neuronal uptake and O-methylation, and in the presence of extraneuronal uptake inhibition by metanephrine. It was also specific for the beta-adrenoceptor, no supersensitivity to histamine being found. In the right atria, the supersensitivity was partially masked by an opposing depressant effect after 6-OHDA pretreatment which was observed with histamine. Dissociation constants (KA) for the left atrial inotropic responses to orciprenaline were determined by use of the antagonist Ro 03-7894. Atria from 6-OHDA-pretreated animals were supersensitive to orciprenaline, but the KA value did not differ from that after sham injection. It could therefore be concluded that the increase in sensitivity was not due to an increase in affinity for the beta-adrenoceptor.
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The supersensitivity was post-synaptic in origin and independent of changes in disposition or metabolism, since it was observed with agonists immune to neuronal uptake and O-methylation, and in the presence of extraneuronal uptake inhibition by metanephrine. It was also specific for the beta-adrenoceptor, no supersensitivity to histamine being found. In the right atria, the supersensitivity was partially masked by an opposing depressant effect after 6-OHDA pretreatment which was observed with histamine. Dissociation constants (KA) for the left atrial inotropic responses to orciprenaline were determined by use of the antagonist Ro 03-7894. Atria from 6-OHDA-pretreated animals were supersensitive to orciprenaline, but the KA value did not differ from that after sham injection. 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identifier ISSN: 0028-1298
ispartof Naunyn-Schmiedeberg's archives of pharmacology, 1985-04, Vol.329 (2), p.162-166
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1432-1912
language eng
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source MEDLINE; SpringerLink Journals
subjects Adrenergic beta-Agonists - pharmacology
Adrenergic beta-Antagonists - pharmacology
Animals
Applied sciences
Benzofurans - pharmacology
Biological and medical sciences
Catecholaminergic system
Dose-Response Relationship, Drug
Exact sciences and technology
Guinea Pigs
Heart - drug effects
Heart Rate - drug effects
Histamine - pharmacology
Hydroxydopamines
In Vitro Techniques
Male
Medical sciences
Metaproterenol - antagonists & inhibitors
Metaproterenol - pharmacology
Myocardial Contraction - drug effects
Neuropharmacology
Neurotransmitters. Neurotransmission. Receptors
Other techniques and industries
Oxidopamine
Pharmacology. Drug treatments
Sympathectomy, Chemical
title Cardiac postjunctional supersensitivity to β-agonists after chronic chemical sympathectomy with 6-hydroxydopamine
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