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. 2010 Sep;161(1):176–192. doi: 10.1111/j.1476-5381.2010.00878.x

Table 3.

Effects of antagonist and enzyme inhibitors on S1P-mediated relaxation in rat CA

pEC50 Rmax n
S1P −7.09 ± 0.3 46.10 ± 4.48 10
S1P (denuded) −6.71 ± 0.77* 23.15 ± 6.82* 8
S1P −7.09 ± 0.3 46.10 ± 4.48 10
S1P + W146 (10 µM) −7.05 ± 0.58 34.74 ± 6.28 5
S1P −7.01 ± 0.37 51.02 ± 6.02 10
S1P + JTE013 (10 µM) −7.62 ± 0.35 55.79 ± 0.36 6
S1P −7.09 ± 0.3 46.10 ± 4.48 10
S1P + CAY10444 (10 µM) −7.99 ± 0.48 20.98 ± 2.65* 5
S1P −7.09 ± 0.3 46.10 ± 4.48 10
S1P + indomethacin (10 µM) −7.29 ± 2.39 9.22 ± 7.77* 4
S1P −7.01 ± 0.37 51.02 ± 6.02 10
S1P + AM630 (10 µM) −6.972 ± 0.42 23.48 ± 3.78* 6
S1P −7.09 ± 0.3 46.10 ± 4.48 10
*S1P + JTE907 (10 µM) −7.19 ± 0.39 18.51 ± 2.44* 5
S1P −7.09 ± 0.3 46.10 ± 4.48 10
S1P + SKi (10 µM) −7.82 ± 0.3 23.14 ± 4.52* 5

Data are expressed as mean ± SEM for n arteries from different animals.

*

P < 0.05 versus S1P alone as determined by two-way anova.