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Properties of P2X and P2Y receptors are dependent on artery diameter in the rat mesenteric bed
Author(s) -
Gitterman D P,
Evans R J
Publication year - 2000
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 - 10.1038/sj.bjp.0703760
Subject(s) - suramin , myograph , receptor , mesenteric arteries , p2 receptor , p2y receptor , ppads , medicine , endocrinology , agonist , purinergic receptor , biology , artery , anatomy , chemistry
P2 receptor mediated contractile responses have been characterized in different diameter arteries from the rat mesenteric arterial vasculature (first, second to third and fifth to sixth order for large, medium and small arteries) using wire myograph and diamtrak video imaging. α,β‐methylene ATP (α,β‐meATP) evoked transient concentration‐dependent contractions in mesenteric arteries with EC 50 values of 0.4, 2.5 and 107 μ M for small, medium and large arteries respectively. Suramin (10–100 μ M ) produced substantial parallel rightward shifts of the concentration‐response curve to α,β‐meATP in small and medium‐sized arteries with pA 2 of 5.1. Responses in large vessels were unaffected by suramin. Immunohistochemical analysis of arterial sections revealed no substantial differences in expression patterns of P2X receptors between different sizes of artery. P2X 1 receptors were expressed at high levels, P2X 4 and P2X 5 receptors were also detected on smooth muscle. The P2X receptor response is dominated by P2X 1 receptor in small and medium arteries but the nature of the receptor mediating the suramin insensitive α,β‐meATP mediated response in large arteries is unclear. The P2Y receptor agonist UTP was significantly more potent in small than in medium or large arteries (EC 50 values: 15.0 μ M small, 88.5 μ M diamtrak medium 1.6 m M myography medium and 1.4 m M large). Responses in both small and medium‐sized vessels were reduced by suramin (30–100 μ M ). The sensitivity to UTP and suramin indicates the presence of P2Y 2 receptors. This study shows that P2 receptors do not have a homogenous phenotype throughout the mesenteric vascular bed and that the properties depend on artery size.British Journal of Pharmacology (2000) 131 , 1561–1568; doi: 10.1038/sj.bjp.0703760