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Actions mediated by P 2 ‐purinoceptorsubtypes in the isolated perfused mesenteric bed of the rat
Author(s) -
Ralevic V.,
Burnstock G.
Publication year - 1988
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1988.tb11686.x
Subject(s) - vasoconstriction , vasodilation , adenosine , purinergic receptor , adenosine triphosphate , chemistry , potency , endocrinology , medicine , perfusion , biology , biochemistry , in vitro
1 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. 2 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. 3 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. 4 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. 5 Removal of the endothelium with sodium deoxycholate totally abolished the vasodilator responses and enhanced the contractile responses. 6 It is concluded that, in the rat mesentery, ATP and its analogues cause vasoconstriction via P 2x ‐purinoceptors and vasodilatation via P 2y ‐purinoceptors and that these are located on the smooth muscle and on the endothelium, respectively.