Publication:
MECHANISM OF CATECHOLAMINE ANTAGONISM IN RAT HEART PRODUCED BY PILOCARPINE AND RELATED DRUGS

dc.contributor.authorC. SADAVONGVIVADen_US
dc.contributor.authorP. SANVARINDAen_US
dc.contributor.authorJUTAMAAD SATAYAVIVADen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-04-19T13:59:38Z
dc.date.available2018-04-19T13:59:38Z
dc.date.issued1974-01-01en_US
dc.description.abstractHigh concentrations of pilocarpine and methacholine consistently lowered the potencies of a series of adrenoceptor agonists as shown by displacement of complete cumulative dose‐effect curves for their positive chronotropic action on rat isolated atria. The order of potency of the agonists was characteristic of β‐adrenoceptor activation and this was converted to the type which characterizes α‐adrenoceptor activation when pilocarpine was present. Propranolol effectively blocked the adrenoceptor agonists in the presence of pilocarpine and phentolamine abolished the antagonistic actions of pilocarpine. Atropine, which by itself did not affect the action of the adrenoceptor agonists, abolished both the bradycardia and antagonism produced by pilocarpine. It is concluded that pilocarpine antagonizes adrenoceptor agonists by muscarinic cholinoceptor activation without involving classical adrenoceptors. 1974 British Pharmacological Societyen_US
dc.identifier.citationBritish Journal of Pharmacology. Vol.52, No.1 (1974), 97-100en_US
dc.identifier.doi10.1111/j.1476-5381.1974.tb09692.xen_US
dc.identifier.issn14765381en_US
dc.identifier.issn00071188en_US
dc.identifier.other2-s2.0-0016259980en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/10726
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0016259980&origin=inwarden_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleMECHANISM OF CATECHOLAMINE ANTAGONISM IN RAT HEART PRODUCED BY PILOCARPINE AND RELATED DRUGSen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0016259980&origin=inwarden_US

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