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The Strathprints institutional repository is a digital archive of University of Strathclyde's Open Access research outputs. Strathprints provides access to thousands of Open Access research papers by University of Strathclyde researchers, including by researchers from the Department of Computer & Information Sciences involved in mathematically structured programming, similarity and metric search, computer security, software systems, combinatronics and digital health.

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Regional variation in p2 receptor expression in the rat pulmonary arterial circulation

Chootip, K. and Ness, K.F. and Wang, Y. and Gurney, A.M. and Kennedy, C. (2002) Regional variation in p2 receptor expression in the rat pulmonary arterial circulation. British Journal of Pharmacology, 137 (5). pp. 637-646. ISSN 1476-5381

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The P2 receptors that mediate contraction of the rat isolated small (SPA, 200–500 μm i.d.) and large (LPA, 1–1.5 mm i.d.) intrapulmonary arteries were characterized. In endothelium-denuded vessels the contractile order of potency was α,β-methyleneATP (α,β-meATP)>>UDP=UTP=ATP=2-methylthioATP>ADP in the SPA and α,β-meATP=UTPUDP>2-methylthioATP, ATP>>ADP in the LPA. α,β-meATP, 2-methylthioATP and ATP had significantly greater effects in the SPA than the LPA (P<0.001), but there was no difference in the potency of UTP or UDP between the vessels. In the SPA, P2X1 receptor desensitisation by α,β-meATP (100 μm) inhibited contractions to α,β-meATP (10 nm–300 μm), but not those to UTP or UDP (100 nm–300 μm). In the LPA, prolonged exposure to α,β-meATP (100 μm) did not desensitize P2X receptors. Pyridoxalphosphate-6-azophenyl-2′,4′-disulphonic acid (PPADS), suramin and reactive blue 2 (RB2) (30–300 μm) inhibited contractions evoked by α,β-meATP. UTP and UDP were potentiated by PPADS, unaffected by RB2 and inhibited, but not abolished by suramin. 1 and 3 mm suramin produced no further inhibition, indicating suramin-resistant components in the responses to UTP and UDP. Thus, both P2X and P2Y receptors mediate contraction of rat large and small intrapulmonary arteries. P2Y agonist potency and sensitivity to antagonists were similar in small and large vessels, but P2X agonists were more potent in small arteries. This indicates differential expression of P2X, but not P2Y receptors along the pulmonary arterial tree.