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. Author manuscript; available in PMC: 2011 Dec 1.
Published in final edited form as: Pharmacol Res. 2010 Sep 17;62(6):465–474. doi: 10.1016/j.phrs.2010.09.002

Table 4.

Pharmacological parameters of vasomotor responses to U46619, PE and S1P in arteries of WT, SPK1−/− and SPK2−/− mice.

pD2 EC50 (µmol/L) Emax (mN/mm)
U46619

Basilar
WT 7.64 ± 0.25 0.02 (0.01–0.07) 0.74 ± 0.06
SPK1−/− 7.80 ± 0.38 0.02 (0.01–0.09) 0.42 ± 0.05**
SPK2−/− 7.27 ± 0.30 0.05 (0.01–0.21) 0.76 ± 0.08

PE

Mesenteric
WT 6.06 ± 0.16 0.87 (0.41–1.84) 1.56 ± 0.10
SPK1−/− 6.13 ± 0.26 0.75 (0.22–2.53) 1.69 ± 0.16
SPK2−/− 6.05 ± 0.17 0.90 (0.41–1.96) 1.65 ± 0.11

S1P

Basilar
WT 6.25 ± 0.25 0.56 (0.18–1.78) 0.60 ± 0.05
SPK1−/− 6.44 ± 0.50 0.36 (0.04–3.63) 0.39 ± 0.06*
SPK2−/− 5.78 ± 0.29 1.65 (0.43–6.36) 0.62 ± 0.07
Mesenteric
WT 6.32 ± 0.25 0.47 (0.15–1.47) 1.29 ± 0.11
SPK1−/− 6.45 ± 0.46 0.36 (0.04–2.99) 1.37 ± 0.19
SPK2−/− 5.58 ± 0.18* 2.69 (1.18–6.14) 1.48 ± 0.14

Pharmacological parameters are from non linear regression; pD2 is the negative logarithm of the concentration producing 50% of the maximum effect, EC50 is the concentration producing 50% of the maximum effect (95% confidence limits are given in parenthesis), Emax is the maximum effect.

Data are mean ± SEM of 5–12 independent measurements. Statistical comparisons were made on the whole curves by two-way ANOVA;

*

P<0.05

**

P<0.01 versus Control.