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Functional characterization of the adenosine receptor mediating inhibition of intestinal secretion
Author(s) -
Hancock Debra L.,
Coupar Ian M.
Publication year - 1995
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.1476-5381.1995.tb14919.x
Subject(s) - adenosine , agonist , adenosine receptor , cgs 21680 , medicine , endocrinology , adenosine a1 receptor , pharmacology , chemistry , antagonist , partial agonist , receptor , biology
1 Previous studies have shown that the mixed A 1 /A 2 adenosine agonist 5′‐N‐ethylcarboxamido‐adenosine (NECA) inhibits intestinal fluid secretion which is thought to contribute to its antidiarrhoeal effect in the rat. The aim of this study was to characterize the adenosine receptor mediating this antisecretory effect via functional studies using a range of selective agonists and antagonists and by applying the pharmacological criteria of relative agonist and antagonist potencies. 2 Adenosine agonists and antagonists were administered i.v. to anaesthetized rats. Intestinal secretion was then stimulated by i.a. infusion of vasoactive intestinal peptide (VIP, 0.8 μg min −1 ) and the net fluid transport across the wall of the jejunum was measured by a recirculation technique. 3 The rank order of agonist potency to reduce the response to VIP was: NECA > N 6 ‐cyclopentyladenosine (CPA) > R‐N 6 ‐(2‐phenylisopropyladenosine) (R‐PIA) > S‐PIA > chloroadenosine (2‐CADO) > 2‐phenylaminoadenosine (CV‐1808). This order best complies with the rank order of agonist potency that represents activation of the recently described A 2B receptor: NECA > 2‐CADO R‐PIA = CHA > S‐PIA > = CV‐1808 > = CGS‐21680. The most potent agonists (NECA, CPA and R‐PIA) had ED 50 values in the low microgram range. 4 The anitsecretory action of NECA (submaximal dose of 40μg kg −1 ) was antagonized equally (approximately 50%) by the selective adenosine antagonists 8‐cyclopentyl‐1,3‐dipropylxanthine (DPCPX, 0.1 mg kg −1 ) and 8‐phenyltheophylline (8‐PT, 0.1 mg kg −1 ). This equipotent activity indicates the presence of an A 2 and not an A 1 receptor. 5 It is suggested that adenosine A 2B receptor agonists could be evaluated for potential use as antidiarrhoeal drugs.