Role of calcium and crossbridges in modulation of rates of force development and relaxation in skinned muscle fibers.

Abstract

The influence of Ca2+ and force generating crossbridges on the kinetics of force development and relaxation was examined in skinned muscle fibers activated by photolytic release of Ca2+ from a caged calcium or inactivated by photolytic uptake of Ca2+ by a caged Ca2+ chelator. In frog fibers at 10 degrees C, decreasing the Ca2+ released from caged calcium to an extent that resulted in 50% of maximum force development produced an approximate seven-fold decrease in the rate of contraction. In contrast decreasing the number of force generating crossbridges by partial extraction of troponin C (TnC) or addition of vanadate caused only minor changes in contraction rate. Thus the rate of force development decreases dramatically with decreases in the Ca2+ level which suggests that a step in the crossbridge cycle may be Ca2+ dependent. The kinetics of relaxation induced by photolysis of diazo-2 was: a) slowed by stabilization of the sarcomeres by repeated releases and re-stretches during contraction and b) accelerated when the amplitude of force development was decreased by decreasing the [Ca2+] which induced a steady contraction. The half time of relaxation decreased by approximately two- to three-fold, when 50% of maximum force was developed. One interpretation of these results is that decreasing the number of force generating crossbridges may speed relaxation by inducing a decreased affinity of TnC for Ca2+ and thus accelerating the Ca2+ dissociation rate from TnC and thereby increasing relaxation rate.