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. 2014 Oct 10;9(10):e109432. doi: 10.1371/journal.pone.0109432

Table 1. Effect of selective inhibitors of NOS (L-NOARG), SK3 (apamin) and IK1 channels (TRAM 34), and combined inhibition of SK3/IK1 channels (A+T) on the ACh and SNAP-induced vasodilation in coronary arteries from LZR and OZR.

ACh
LZR OZR
pEC50 Emax ΔBT n pEC50 Emax ΔBT n
control 7.01±0.19 91±3 - 7 6.9±0.15 90±5 - 6
L-NOARG - 2±8 c 25±14 7 - 22±6c 31±13 6
control 6.8±0.16 87±6 - 7 6.8±0.13 93±2 - 8
apamin 7.0±0.18 a 73±5 a 9±3 7 6.42±0.10a 80±4b 14±5 8
control 7.0±0.2 90±2 - 6 6.9±0.19 86±3 - 9
TRAM34 6.9±0.13 73±6 a 9±6 6 6.43±0.16a 65±5c 25±6 9
control 6.9±0.22 89±6 - 9 6.9±0.25 90±4 - 6
A+T 6.8±0.19 74±3 b 10±2 9 6.1±0.14b 68±1c 35±8# 6

Values represent mean ± S.E.M. of the number n of individual arteries. pEC50 is –logEC50. Emax is maximal relaxation expressed as percentage of 5-HT-induced precontraction. ΔBT; is the increase in basal tension expressed as percentage of KPSS-induced contraction. Significant differences from controls were analyzed using paired t test; a P <0.05; b P <0.01; c P <0.001 vs control; or one way ANOVA followed by a Bonferroni test for across-group comparisons; # P <0.05 vs A+T-treated LZR; P <0.05 vs TRAM34-treated LZR.