Skip to main content
. 2002 Mar;135(5):1324–1330. doi: 10.1038/sj.bjp.0704575

Figure 1.

Figure 1

Relative potency of adenosine receptor agonists to relax rabbit cranial mesenteric arteries. The mesenteric artery rings were pre-contracted with noradrenaline (10 μM) and the functionality of the endothelium was verified by testing the response to acetylcholine. Then, cumulative concentration-response curves with increasing concentrations of the selective A2A receptor agonist, CGS 21680, of the mixed A1/A2 receptor agonist, NECA, or with the closest non-metabolizable adenosine analogue, CADO, were carried out in (a). In (b), cumulative concentration-response curves with increasing concentrations of CADO were performed either in the absence or in the presence of the selective A2A receptor antagonist, ZM 241385 (100 nM). The data are mean±s.e.mean of 5 – 6 experiments.