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. 2010 Sep;161(1):207–228. doi: 10.1111/j.1476-5381.2010.00889.x

Table 9.

Inhibitory effects of GSK1562590 (1 mg·kg−1, p.o.) on hU-II-induced contraction of rat aorta ex vivo

hU-II pEC50 hU-II Emax (% 60 mM KCl)
Time (h) Plasma concentration (nM) Vehicle GSK1562590 Vehicle GSK1562590
2 1.10 ± 0.35 8.35 ± 0.07 8.07 ± 0.18 66 ± 37 23 ± 9*
16 <0.12 ± 0.04 8.52 ± 0.05 8.27 ± 0.09* 64 ± 8 27 ± 5*
24 <0.07 8.46 ± 0.02 8.29 ± 0.09 106 ± 6 54 ± 16*
36 <0.07 8.65 ± 0.05 8.61 ± 0.05 117 ± 11 91 ± 14
48 <0.07 8.56 ± 0.05 8.49 ± 0.07 102 ± 9 102 ± 12

All values are expressed as mean ± SEM (n= 5–7).

Plasma concentrations below limit of detection (0.07 nM) for four out of six animals. Statistical comparisons of Emax and pEC50 values were made using unpaired, two-tailed t-tests where

*

P < 0.05 versus vehicle.