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. 2011 May 27;301(2):H391–H401. doi: 10.1152/ajpheart.00336.2011

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Fig. 9. — Line graphs illustrate the concentration-dependent effects of 2′,3′-cAMP on [³H]thymidine incorporation (A) and cell number (B) in human CAVSMCs. Bar graph (C) illustrates effects of DPCPX (A₁ antagonist), SCH-58261 (A_2A antagonist), MRS-1754 (A_2B antagonist), and VUF-5574 (A₃ antagonist) (each at 0.1 μmol/l) on inhibition of [³H]thymidine incorporation by 2′,3′-cAMP (30 μmol/l) in human CAVSMCs. P values are from 1-factor ANOVA. ^aP < 0.05 (Fisher's LSD test) compared with basal (0) (A and B) or compared with no inhibitor (C).