Skip to main content
. 2003 Nov 3;140(7):1193–1200. doi: 10.1038/sj.bjp.0705549

Table 1.

Summary of the effects of different agents or treatments on pEC50 values and maximal relaxations to H2O2 in PGF2α contracted mouse SMA

Treatment n pEC50 Maximal relaxationa (%)
Control (EC+) 8 4.54±0.13 94.4±1
Control (EC−) 5 4.6±0.2 95.1±1
Indomethacin 10 μM 4 4.57±0.14 93.7±1
ODQ 10 μM 6 4.51±0.18 94.8±1
EDTA 0.067 mM 4 4.37±0.04 96.6±1
3-AT 50 mM 4 4.58±0.03 93.2±1
KCl 25 mM 4 4.31±0.06 87.1±1b
TEA 10 mM 4 4.27±0.06 94.8±1
Ap 1 μM/ChTx 100 nM 4 4.57±0.04 97.6±1
4-AP 1 mM 4 4.38±0.11 93.8±1
TEA/4-AP 4 4.79±0.05 91.2±2
Oua 100 μM/Ba2+ 30 μM 4 4.52±0.1 90.3±5
a

Maximal relaxations are expressed as percentages of the contraction to PGF2α (0.01–0.1 μM).

b

P<0.05 when compared to control (EC+), ANOVA, followed by Dunnett's multiple comparison test.

3-AT: 3-amino-1,2,4-triazole; 4-AP: 4-aminopyridine; Ap: apamin; Ba2+: barium chloride; ChTx: charybdotoxin; EC+: endothelium-intact; EC−: endothelium-denuded; EDTA: ethylene diamine tetraacetic acid; H2O2: hydrogen peroxide; KCl: potassium chloride; ODQ: 1-H[1,2,4]oxadiazolo[4,3-]quinoxalin-1-one; oua: ouabain; pEC50: −log[EC50]; TEA: tetraethylammonium.