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10.1111/j.1365-2125.1982.tb01911.x

http://scihub22266oqcxt.onion/10.1111/j.1365-2125.1982.tb01911.x
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suck abstract from ncbi


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pmid6125170      Br+J+Clin+Pharmacol 1982 ; 13 (Suppl 2): 199S-200S
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  • Relevance of selectivity and non-selectivity in beta-adrenoceptor blocking drugs #MMPMID6125170
  • Bonelli J
  • Br J Clin Pharmacol 1982[]; 13 (Suppl 2): 199S-200S PMID6125170show ga
  • 1 The heart rate responses to increasing doses of isoprenaline (n = 6) (during infusion with atropine 0.5 mg/min i.v.) and noradrenaline (n = 5), (during infusion with phentolamine 160 mg/h i.v.) were recorded before and after the intravenous administration of propranolol (15 mg) or metoprolol (15 mg). 2 In the doses used, metoprolol was less potent than propranolol in antagonizing isoprenaline-induced tachycardia, during atropine infusion. 3 In volunteers treated with phentolamine both metoprolol and propranolol produced similar inhibition of noradrenaline-induced tachycardia, indicating comparable beta 1-adrenoceptor blockade in the doses used. 4 The fact that the shift of the dose-response curve of isoprenaline-induced tachycardia was smaller after metoprolol than after propranolol supports the hypothesis that beta 2-adrenoceptors are present in the heart.
  • |Adrenergic beta-Antagonists/*pharmacology[MESH]
  • |Adult[MESH]
  • |Atropine/pharmacology[MESH]
  • |Dose-Response Relationship, Drug[MESH]
  • |Heart Rate/drug effects[MESH]
  • |Humans[MESH]
  • |Isoproterenol/pharmacology[MESH]
  • |Male[MESH]
  • |Metoprolol/pharmacology[MESH]
  • |Norepinephrine/pharmacology[MESH]
  • |Organ Specificity[MESH]


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