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 in | British journal of pharmacology Vol. 81; no. 2; pp. 401 - 407 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.02.1984
Nature Publishing Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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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. |
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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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Cites_doi | 10.1111/j.1476-5381.1983.tb09381.x 10.1113/jphysiol.1973.sp010125 10.1016/0024-3205(79)90458-2 10.1111/j.1748-1716.1979.tb06321.x 10.1093/cvr/17.4.192 10.1111/j.1476-5381.1959.tb00928.x 10.1161/01.CIR.35.4.745 10.1152/ajplegacy.1963.204.6.969 10.1016/0014-2999(82)90341-7 10.1007/978-94-009-5816-6_4 10.1111/j.1600-0773.1981.tb00913.x 10.1016/0014-2999(79)90241-3 10.1111/j.1440-1681.1981.tb00148.x 10.1016/0006-2952(71)90440-0 |
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References | 1971; 20 1979; 105 1980; 238 1970; 186 1979; 24 1965; 149 1982; 81 1982; 3 1963; 204 1981; 49 1981; 8 1967; 35 1983 1972; 30 1981 1980 1959; 14 1973; 229 1983; 17 1979; 60 1947; 90 1983; 78 Nayler W.G. (e_1_2_1_17_1) 1963; 204 Devous M.D. (e_1_2_1_8_1) 1983 Hillis W.S. (e_1_2_1_11_1) 1982; 3 Walton R.P. (e_1_2_1_23_1) 1947; 90 e_1_2_1_7_1 Blinks J.R. (e_1_2_1_4_1) 1972; 30 e_1_2_1_20_1 e_1_2_1_5_1 e_1_2_1_6_1 e_1_2_1_3_1 e_1_2_1_12_1 James T.N. (e_1_2_1_13_1) 1965; 149 e_1_2_1_10_1 e_1_2_1_21_1 e_1_2_1_2_1 e_1_2_1_16_1 Fredholm B.B. (e_1_2_1_9_1) 1980 e_1_2_1_14_1 Lammerant J. (e_1_2_1_15_1) 1970; 186 Thompson C.I. (e_1_2_1_22_1) 1980; 238 e_1_2_1_18_1 e_1_2_1_19_1 |
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Pharmac. – volume: 20 start-page: 3359 year: 1971 end-page: 3365 article-title: A species difference in the uptake of adenosine by the heart publication-title: Biochem. Pharmac. – volume: 229 start-page: 41 year: 1973 end-page: 49 article-title: Left ventricular contractility and developed tension in the intact dog submitted to an intracoronary infusion of adenosine publication-title: J. Physiol. – volume: 8 start-page: 171 year: 1981 end-page: 174 article-title: Inotropic responses of isolated atrial and ventricular muscle from the dog heart to inosine, guanosine and adenosine publication-title: Clin. exp. Pharmac. Physiol. – volume: 24 start-page: 2475 year: 1979 end-page: 2482 article-title: Alkylxanthines: inhibition of adenosine elicited accumulation of cyclic AMP in brain slices and of brain phosphodiesterase activity publication-title: Life Sci. – volume: 14 start-page: 48 year: 1959 end-page: 58 article-title: Some quantitative uses of drug antagonists publication-title: Br. 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Ther. contributor: fullname: James T.N. – start-page: 507 volume-title: Regulatory function of adenosine year: 1983 ident: e_1_2_1_8_1 contributor: fullname: Devous M.D. – start-page: 129 year: 1980 ident: e_1_2_1_9_1 article-title: Are methylxanthine effects due to antagonism of endogenous adenosine publication-title: T.I.P.S. contributor: fullname: Fredholm B.B. – ident: e_1_2_1_3_1 doi: 10.1161/01.CIR.35.4.745 – volume: 204 start-page: 969 year: 1963 ident: e_1_2_1_17_1 article-title: Effect of caffeine on cardiac contractile activity and radio‐calcium movement publication-title: Am. J. Physiol. doi: 10.1152/ajplegacy.1963.204.6.969 contributor: fullname: Nayler W.G. – ident: e_1_2_1_7_1 doi: 10.1016/0014-2999(82)90341-7 – ident: e_1_2_1_19_1 doi: 10.1007/978-94-009-5816-6_4 – ident: e_1_2_1_18_1 doi: 10.1111/j.1600-0773.1981.tb00913.x – volume: 238 start-page: H389 year: 1980 ident: e_1_2_1_22_1 article-title: Changes in adenosine and glycogen phosphorylase activity during the cardiac cycle publication-title: Am. J. Physiol. contributor: fullname: Thompson C.I. – volume: 186 start-page: 166 year: 1970 ident: e_1_2_1_15_1 article-title: Changes in the calculated myocardial oygen consumption during adenosine infusion versus estimates of developed tension and velocity of contraction publication-title: Arch. int. Pharmacodyn. contributor: fullname: Lammerant J. – ident: e_1_2_1_16_1 doi: 10.1016/0014-2999(79)90241-3 – ident: e_1_2_1_5_1 doi: 10.1111/j.1440-1681.1981.tb00148.x – ident: e_1_2_1_12_1 doi: 10.1016/0006-2952(71)90440-0 |
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We investigated the possibility that the positive inotropic effects of the alkylxanthines are due to adenosine receptor blockade.
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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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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 |
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