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. 2017 Oct 24;7:13901. doi: 10.1038/s41598-017-14472-z

Figure 5.

Figure 5

The DA D2 receptor antagonist, L-741,626, blocks RO5256390’s effects on cocaine-induced changes in DA transport. Co-application of cocaine (Co) with the DA D2 receptor antagonist, L-741,626 (L-741), dose-dependently increased cocaine effects on DA release (a). This effect was also observed with the perfusion of the lower concentration of L-741 alone. Sumanirole (Suman), DA D2 receptor agonist dose-dependently produced a significant attenuation of cocaine’s effect on tau whereas L-741,626 significantly potentiated cocaine’s effect on tau (b). The lower concentration of L-741,626 (30 nM), which did not affect cocaine-induced changes in DA clearance when perfused with RO5256390 and cocaine, completely blocked RO5256390’s ability to inhibit cocaine’s effects on DA uptake (d). SB216763 (SB), a GSK-3 inhibitor, increased peak at the lower concentration (e) and significantly attenuated cocaine-induced DA increases in tau at the higher concentration (f). (*p < 0.05, **p < 0.01 vs baseline; #p < 0.05, ##p < 0.01 vs cocaine values; n = 5–19).