Actions mediated by P2‐purinoceptorsubtypes in the isolated perfused mesenteric bed of the rat
Open Access
- 1 October 1988
- journal article
- research article
- Published by Wiley in British Journal of Pharmacology
- Vol. 95 (2) , 637-645
- https://doi.org/10.1111/j.1476-5381.1988.tb11686.x
Abstract
The effects of adenosine 5′‐triphosphate (ATP) and its analogues on the perfusion pressure of the isolated mesenteric bed of the rat were examined in preparations at resting tone, and with tone raised by noradrenaline. In the preparations at resting tone, the effect of the analogues was to produce vasoconstriction, their rank order of potency being α,β‐methylene ATP > 2‐methylthio ATP > ATP. In raised tone preparations, dose‐dependent vasodilatations were produced by ATP and 2‐methylthio ATP although, at the highest doses tested, responses decreased in magnitude. The rank order of potency of the analogues in eliciting this vasodilator response was 2‐methylthio ATP > ATP, while α,β‐methylene ATP was without effect. Following desensitization of contractile responses to α,β‐methylene ATP, contractile responses to ATP and 2‐methylthio ATP were abolished while their relaxant responses were potentiated. Removal of the endothelium with sodium deoxycholate totally abolished the vasodilator responses and enhanced the contractile responses. It is concluded that, in the rat mesentery, ATP and its analogues cause vasoconstriction via P2x‐purinoceptors and vasodilatation via P2y‐purinoceptors and that these are located on the smooth muscle and on the endothelium, respectively.This publication has 38 references indexed in Scilit:
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