Diuretic and saliuretic effects of 1,3-dipropyl-8-cyclopentylxanthine, a selective A1-adenosine receptor antagonist
- 1 February 1991
- journal article
- Published by Oxford University Press (OUP) in Journal of Pharmacy and Pharmacology
- Vol. 43 (2) , 138-139
- https://doi.org/10.1111/j.2042-7158.1991.tb06651.x
Abstract
We have previously shown that 8-phenyltheophylline (8-PT), a non-selective antagonist at adenosine A1-and A2-receptors, has a diuretic effect. In this study, the diuretic and adenosine antagonist effects of the A1-receptor selective compound 1,3-dipropyl-8-cyclopentylxanthine (CPX) have been examined in the conscious rat. CPX (0.1 and 0.3 mg kg−1 i.v.) significantly attenuated bradycardic but not hypotensive responses evoked by adenosine. In contrast, 8-PT (3 mg kg−1 i.v.) significantly antagonized both adenosine-induced bradycardia and hypotension. CPX (0.1 and 0.3 mg kg−1 i.v.) evoked a dose-related diuretic and saliuretic response in the conscious rat. These results indicate that the diuretic effects of adenosine antagonists are associated with blockade of the A1-receptor sub-type.Keywords
This publication has 12 references indexed in Scilit:
- Amelioration of glycerol-induced acute renal failure in the rat with 8-cyclopentyl-1,3-dipropylxanthineBritish Journal of Pharmacology, 1989
- Apparent affinity of 1,3‐dipropyl‐8‐cyclopentylxanthine for adenosine A1 and A2 receptors in isolated tissues from guinea‐pigsBritish Journal of Pharmacology, 1989
- PD 116,948, a highly selective A1 adenosine receptor antagonistLife Sciences, 1987
- Adenosine induces a calcium-dependent glomerular contractionEuropean Journal of Pharmacology, 1987
- The adenosine receptor antagonist, 8-phenyltheophylline, causes diuresis and saliuresis in the ratJournal of Pharmacy and Pharmacology, 1986
- Effects of adenosine receptor agonists in the isolated, perfused rat kidneyAmerican Journal of Physiology-Heart and Circulatory Physiology, 1984
- A method for screening diuretic agents in the ratJournal of Pharmacological Methods, 1984
- Adenosine relaxes the aorta by interacting with an A2 receptor and an intracellular siteEuropean Journal of Pharmacology, 1983
- Adenosine A1 receptor mediated inhibition of nerve stimulation-induced contractions of the rabbit portal veinEuropean Journal of Pharmacology, 1983
- Inhibitory effect of adenosine on adrenergic neuroeffector transmission in the rabbit heartActa Physiologica Scandinavica, 1979