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. 2013 Jul 26;169(8):1810–1823. doi: 10.1111/bph.12262

Figure 5.

Figure 5

Activation of A3 receptors by endogenous adenosine prevented the effect of inosine in 15 mM K+. (A) Inosine (100 μM) failed to reduce asynchronous ACh release induced by 15 mM K+ (n = 5). (B) The inhibition of the production of adenosine by 100 μM αβ-MeADP (inhibitor of ecto-5′-nucleotidase, n = 4) allowed the effect of 100 μM inosine on 15 mM K+-evocked ACh release. (C) Blockade of A3 receptors with the selective antagonist MRS-1191 (5 μM) prevented the inhibitory action of endogenous nucleosides and further increased MEPP frequency in 15 mM K+ (n = 4). Data (mean ± SEM) are expressed as percentage of control values. **P < 0.01, *P < 0.05, anova followed by Tukey's test.