INTERACTION OF IBERIOTOXIN WITH BETA-ADRENOCEPTOR AGONISTS AND SODIUM-NITROPRUSSIDE ON GUINEA-PIG TRACHEA

Airway smooth muscle plasma membranes contain a variety of functional K+ channels. In particular, there is a predominance of Ca2+-activated K+ channels (maxi-K). Inhibition of these K+ channels has been postulated to account for the ability of charybdotoxin (ChTX) to produce contraction of airway smooth muscle and to modify the relaxant effects of beta-adrenoceptor agonists and sodium nitroprusside (SNP). Iberiotoxin (IbTX) is more selective and more potent than ChTX at blocking maxi-K channels. In this study, pharmacological experiments were performed on guinea pig trachea to determine whether IbTX produced effects similar to ChTX. The concentration-response curves to isoproterenol were shifted to the right (13- and 18-fold) by 60 and 180 nM IbTX, respectively. Concentration-response curves to salbutamol were markedly affected by IbTX, with a >60-fold rightward shift being produced with 20 nM IbTX. The maximal relaxation to salbutamol was reduced to 49.3 +/- 0.9, 22.3 +/- 4.7, and 15.0 +/- 2.7% of control maximum in the presence of 20, 60, and 180 nM IbTX, respectively. Similar to salbutamol, the maximal relaxation to SNP was reduced to 80 +/- 1.6, 19 +/- 1.7, and 12 +/- 2.1% of control maximum in the presence of 20, 60, and 180 nM IbTX, respectively. IbTX (180 nM) failed to produce a significant alteration of relaxation to the ATP-dependent K+ channel agonist BRL-34915. Exposure of tissues to K+-rich medium (80 mM) inhibited responses to salbutamol greater-than-or-equal-to SNP > isoproterenol. These results confirm and extend our earlier observations that maxi-K channels may be involved in regulating tone and relaxation of carbachol-contracted guinea pig tracheal smooth muscle. This mechanism is of particular importance for beta2-adrenoceptor- and SNP-induced relaxation.