Abstract
The 78,000 x g microsomal fraction of canine ventricular myocardium effected a 20-fold concentration of [(3)H]norepinephrine from a 10(-9) M solution. The [(3)H]norepinephrine bound was displaced by physiologic concentrations of the beta-adrenergic catecholamines isoproterenol, epinephrine, and norepinephrine, in that order, which is the order of effectiveness of their actions on the force and rate of cardiac contraction. Alpha-adrenergic compounds did not displace [(3)H]norepinephrine until concentrations four orders of magnitude greater were reached. The beta-adrenergic blocker propranolol displaced at 10(-6) M, whereas the alpha-adrenergic blocker phentolamine was inactive. Metabolites of the catecholamines did not compete for this binding site. It is concluded that, on the basis of specificity and affinity of binding, these microsomal particles are likely to contain the beta-adrenergic receptor.
MeSH Terms
Adrenergic alpha-Antagonists/metabolism
Adrenergic beta-Antagonists/metabolism
Animals
Autoradiography
Binding Sites
Catecholamines/pharmacology
Dihydroxyphenylalanine/metabolism
Dogs
Dopamine/metabolism
Epinephrine/metabolism
Heart/drug effects
Heart Ventricles/cytology,metabolism
Isoproterenol/metabolism
Microsomes/metabolism
Myocardium/cytology,metabolism
Norepinephrine/antagonists & inhibitors,metabolism
Phentolamine/metabolism
Propranolol/metabolism
Receptors, Adrenergic
Receptors, Drug
Sympathomimetics/pharmacology
Tritium
Chemicals
Adrenergic alpha-Antagonists
Adrenergic beta-Antagonists
Catecholamines
Receptors, Adrenergic
Receptors, Drug
Sympathomimetics
Tritium
Dihydroxyphenylalanine
Propranolol
Isoproterenol
Dopamine
Norepinephrine
Epinephrine
Phentolamine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lefkowitz R J
Haber E
References (12)
12 references, click to expand
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