Evidence that the positive inotropic effects of the alkylxanthines are not due to adenosine receptor blockade

1 We investigated the possibility that the positive inotropic effects of the alkylxanthines are due to adenosine receptor blockade. 2 The potency of 8‐phenyltheophylline, theophylline and enprofylline as adenosine antagonists was assessed in vitro, using the guinea‐pig isolated atrium, and in vivo,...

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Published inBritish journal of pharmacology Vol. 81; no. 2; pp. 401 - 407
Main Authors Collis, M.G., Keddie, J.R., Torr, S.R.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.02.1984
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Abstract 1 We investigated the possibility that the positive inotropic effects of the alkylxanthines are due to adenosine receptor blockade. 2 The potency of 8‐phenyltheophylline, theophylline and enprofylline as adenosine antagonists was assessed in vitro, using the guinea‐pig isolated atrium, and in vivo, using the anaesthetized dog. 3 The order of potency of the alkylxanthines as antagonists of the negative inotropic response to 2‐chloroadenosine in vitro, and of the hypotensive response to adenosine in vivo was 8‐phenyltheophylline > theophylline > enprofylline. 4 The order of potency of the alkylxanthines as positive inotropic and chronotropic agents in the anaesthetized dog was enprofylline > theophylline > 8‐phenyltheophylline. 5 The results of this study indicate that the inotropic effects of the alkylxanthines in the anaesthetized dog are not due to adenosine receptor blockade.
AbstractList We investigated the possibility that the positive inotropic effects of the alkylxanthines are due to adenosine receptor blockade. The potency of 8-phenyltheophylline, theophylline and enprofylline as adenosine antagonists was assessed in vitro, using the guinea-pig isolated atrium, and in vivo, using the anaesthetized dog. The order of potency of the alkylxanthines as antagonists of the negative inotropic response to 2-chloroadenosine in vitro, and of the hypotensive response to adenosine in vivo was 8-phenyltheophylline greater than theophylline greater than enprofylline. The order of potency of the alkylxanthines as positive inotropic and chronotropic agents in the anaesthetized dog was enprofylline greater than theophylline greater than 8-phenyltheophylline. The results of this study indicate that the inotropic effects of the alkylxanthines in the anaesthetized dog are not due to adenosine receptor blockade.
1 We investigated the possibility that the positive inotropic effects of the alkylxanthines are due to adenosine receptor blockade. 2 The potency of 8‐phenyltheophylline, theophylline and enprofylline as adenosine antagonists was assessed in vitro, using the guinea‐pig isolated atrium, and in vivo, using the anaesthetized dog. 3 The order of potency of the alkylxanthines as antagonists of the negative inotropic response to 2‐chloroadenosine in vitro, and of the hypotensive response to adenosine in vivo was 8‐phenyltheophylline > theophylline > enprofylline. 4 The order of potency of the alkylxanthines as positive inotropic and chronotropic agents in the anaesthetized dog was enprofylline > theophylline > 8‐phenyltheophylline. 5 The results of this study indicate that the inotropic effects of the alkylxanthines in the anaesthetized dog are not due to adenosine receptor blockade.
We investigated the possibility that the positive inotropic effects of the alkylxanthines are due to adenosine receptor blockade. The potency of 8‐phenyltheophylline, theophylline and enprofylline as adenosine antagonists was assessed in vitro , using the guinea‐pig isolated atrium, and in vivo , using the anaesthetized dog. The order of potency of the alkylxanthines as antagonists of the negative inotropic response to 2‐chloroadenosine in vitro , and of the hypotensive response to adenosine in vivo was 8‐phenyltheophylline > theophylline > enprofylline. The order of potency of the alkylxanthines as positive inotropic and chronotropic agents in the anaesthetized dog was enprofylline > theophylline > 8‐phenyltheophylline. The results of this study indicate that the inotropic effects of the alkylxanthines in the anaesthetized dog are not due to adenosine receptor blockade.
Author Collis, M.G.
Keddie, J.R.
Torr, S.R.
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Snippet 1 We investigated the possibility that the positive inotropic effects of the alkylxanthines are due to adenosine receptor blockade. 2 The potency of...
We investigated the possibility that the positive inotropic effects of the alkylxanthines are due to adenosine receptor blockade. The potency of...
We investigated the possibility that the positive inotropic effects of the alkylxanthines are due to adenosine receptor blockade. The potency of...
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proquest
crossref
pubmed
pascalfrancis
wiley
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SubjectTerms Animals
Atenolol - pharmacology
Biological and medical sciences
Cardiotonic agents
Cardiovascular system
Dogs
Female
Guinea Pigs
Heart Atria - drug effects
Heart Rate - drug effects
Hydrogen-Ion Concentration
In Vitro Techniques
Male
Medical sciences
Myocardial Contraction - drug effects
Pharmacology. Drug treatments
Receptors, Cell Surface - antagonists & inhibitors
Receptors, Purinergic
Xanthines - pharmacology
Title Evidence that the positive inotropic effects of the alkylxanthines are not due to adenosine receptor blockade
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1476-5381.1984.tb10092.x
https://www.ncbi.nlm.nih.gov/pubmed/6322898
https://search.proquest.com/docview/81006312
https://pubmed.ncbi.nlm.nih.gov/PMC1986898
Volume 81
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