INHIBITION BY AMILORIDE OF CONTRACTILE ELEMENTS IN SMOOTH-MUSCLE OF GUINEA-PIG TAENIA CECUM AND CHICKEN GIZZARD

  • 1 October 1987
    • journal article
    • research article
    • Vol. 243  (1) , 370-377
Abstract
The relaxant action of amiloride was investigated inthe smooth muscles of guinea pig taenia ceci and chicken gizzard. Amiloride inhibited the contractions induced by high K+ (45.4 mM) and carbachol (10 .mu.M) in the taenia with the concentrations needed to induce 50% inhibition (IC50) of approximately 41 .mu.M. A prolonged incubation period (> 1 hr) was necessary to obtain the full inhibition of these contractions. The taenia gradually accumulated amiloride and the tissue/medium ratio exceeded 2.0 after a 120-min incubation period. Amiloride had no effect on the high K+-stimulated 45Ca++ uptake or the ATP content of the taenia. Amiloride inhibited the Ca++-induced contraction of the saponintreated taenia with an IC50 of 186 .mu.M. Amiloride (10-1000 .mu.M) also inhibited superprecipitation and Mg++-adenosine triphosphatase activity of the gizzared native actomyosin as well as the phosphorylation of myosin light chain. The inhibition of the phosphorylation was antagonized competitively by ATP. Amiloride (1 mM) had no effect on the dephosphorylation of myosin light chain upon removal of CA++ from reaction medium. Amiloride, at concentrations up to 1 mM, had not effect on calmodulin activity as monitored by the Ca++-calmodulin-activated erythrocyte membrane (Ca++ + Mg++)-adenosine triphosphatase and phosphodiesterase activities. In contrast to this, trifluoperazine inhibited the calmodulin activity at the concentration needed to inhibit the Ca++-induced contraction of the permeabilized taenia and the superprecipitation and the phosphorylation of myosin light chain of gizzard. We conclude that amiloride, unlike trifluoperazine, may inhibit directly the myosin light chain kinase activity to induce muscle relaxation.