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. 2012 Jun 19;10(6):e1001347. doi: 10.1371/journal.pbio.1001347

Figure 4. Cross-antagonism between D4 and α1B or β1 receptors in transfected cells and in pineal gland.

Figure 4

In (A to D) CHO cells were transiently co-transfected with 2 µg of plasmid coding for D4 receptors and with 3 µg of plasmid coding for α1B receptors (A and B) or β1 receptors (C and D). In (E and F) rat pineal glands were extracted at 9:00 h and processed as indicated in Materials and Methods. Cells were treated for 7 min and pineal glands were treated for 10 min with 500 nM of RO 10-5824 (RO), phenylephrine (Phenyl), or isoproterenol (Iso) or with 1 µM of L-745,870 (L-745), REC 15/2615 (REC), or CGP 20712 (CGP), alone or in combination. The immunoreactive bands, corresponding to ERK 1/2 (Thr183-Tyr185) phosphorylation (A, C, and E) and Akt (Ser473) phosphorylation (B, D, and F) of four experiments were quantified and values represent the mean ± S.E.M. of the fold increase with respect to basal levels found in untreated cells. Significant differences were calculated by a one-way ANOVA followed by post hoc Bonferroni's tests (***p<0.001, as compared to the basal level; # p<0.001, as compared to the sample treated with RO 10-5824; $ p<0.001, as compared to the sample treated with phenylephrine; & p<0.001, as compared to the sample treated with isoproterenol). A representative Western blot is shown at the top of each panel.