TABLE 2

Effects of signaling inhibitors on 10 μM forskolin-induced relaxation of rat bladder strips Data are means ± S.E.M. of 5 to 13 experiments and are expressed as a percentage of relaxation. ODQ was compared with dimethylsulphoxide, glibenclamide and H89 to ethanol, apamin to acetic acid, and all other inhibitors to deionized water. Note that the Rp-cAMPS experiments were done at a later point in time and hence were compared with a different control group (against passive, 39 ± 5% and against KCl, 74 ± 3%; n = 6 each).




Against Passive Tension

Against KCl-Induced Precontraction
Absence of inhibitors
   H2O 37 ± 3 70 ± 2
   Ethanol 38 ± 3 73 ± 1
   DMSO 42 ± 4 70 ± 2
   Acetic acid 37 ± 3 61 ± 6
Cyclic nucleotide-dependent pathways
   SQ 22,536 26 ± 3 74 ± 3
   H7 27 ± 3 73 ± 1
   H89 38 ± 5 66 ± 5
   Rp-cAMPS 23 ± 3* 75 ± 2
   ODQ 30 ± 3 72 ± 3
   l-NNA 29 ± 4 67 ± 3
Potassium channels
   BaCl2 44 ± 4 73 ± 2
   Tetraethylammonium 35 ± 6 69 ± 4
   Glibenclamide 35 ± 7 64 ± 2
   Apamin 43 ± 4 63 ± 2
   Charybdotoxin 45 ± 4 49 ± 2*
   Iberiotoxin 41 ± 6 56 ± 1*
Combinations
   SQ + ODQ 17 ± 3* 59 ± 3*
   SQ + charybdotoxin 32 ± 3 46 ± 1*
   ODQ + charybdotoxin 41 ± 3 51 ± 1*
   SQ + ODQ + charybdotoxin
17 ± 3*
49 ± 2*
  • DMSO, dimethyl sulfoxide.

  • * P < 0.05 vs. corresponding vehicle control in a two-tailed t test or one-way analysis of variance followed by Dunnett's tests