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. 2011 Sep;164(2b):471–484. doi: 10.1111/j.1476-5381.2011.01401.x

Figure 8.

Figure 8

Upper GI transit in vivo in wild-type (WT), single and double peptide null mice following vehicle (control) or Y1 or Y2 receptor antagonists. Transit was increased significantly in PYY−/− compared with WT transit rates (Student's unpaired t-test; *P≤ 0.05). The effects of Y1 (BIBO3304, 0.4 mM·100 µL−1, i.p.) or Y2 (BIIE0246, 60 µg·100 µL−1, i.p.) receptor antagonists on transit are shown for each genotype. There were no statistical differences between antagonist-treated transit rates and controls in WT, NPY−/− or PYY−/− mice. However, the inhibitory effects of both antagonists in PYY−/− were significantly different from the slight prokinetic effects of both antagonists in WT controls (two-way anova, no asterisk shown). Each bar is the mean + SEM from number of assays in parenthesis.