Caffeine application to isolated rat ventricular myocytes produced an increase in intracellular calcium and contracture, with the contracture shape depending on application speed and concentration.
In isolated rat ventricular myocytes, caffeine-induced contractures depend on both transient increases in intracellular calcium and calcium-independent sensitization of myofilaments by intracellular caffeine.
Fluorescence measurements have been made in single, isolated rat ventricular myocytes using the Ca2(+)-sensitive indicators Fura-2 and Indo-1. In Fura-2-loaded cells, the application of caffeine (2-20 mM) produced a change of fluorescence indicating an increase of Ca2+i which then spontaneously decayed to control levels. These changes of Ca2+i were accompanied by a contracture. 2. In contrast, in Indo-1-loaded cells, in addition to the changes of fluorescence expected for the transient increase of Ca2+i produced by caffeine, there was a maintained decrease of fluorescence. 3. Measurements in vitro showed that caffeine quenches the fluorescence of Indo-1 (but not of Fura-2) in a Ca2+-and wavelength-independent manner. Caffeine therefore had no effect on the ratio of Indo-1 fluorescence measured at two wavelengths. This inhibition by caffeine could be described by an apparent Ki of 4 mM. In the cell the Ki was considerably larger (18 mM). 4. We have separated the Indo-1 fluorescence changes into caffeine- and Ca2+i-dependent components. The time course of change of intracellular caffeine was calculated. When caffeineo was rapidly increased, caffeinei changed with a rate constant of 8 s-1 giving an apparent permeability to caffeine of 2 x 10(-3) cm s-1. 5. This method was used to measure caffeinei and Ca2+i simultaneously during caffeine-induced contractures. The shape of the caffeine contracture was found to depend on both the speed of application of caffeine and the concentration applied. If caffeine was applied quickly then the contracture developed within 1 s to a maximum level and then relaxed to a lower maintained level. With slower application, there was a more complete relaxation of the initial contraction followed by a slower redevelopment of contraction. 6. Despite the difference in contraction time course, irrespective of the flow rate, Ca2+i decayed monotonically. The slow secondary development of contraction has the same time course as the increase of caffeinei. The caffeine contracture can be reproduced by a model in which both Ca2+i and caffeinei affect contraction. 7. The increase of Ca2+i is not greatly affected by altering the caffeine concentration from 2.5 to 50 mM. In contrast the maintained level of contraction increases over this range showing that the Ca2(+)-independent effects of caffeine on the myofilaments have a low affinity for caffeine.
O’Neill et al. (1990) studied this question. Caffeine was evaluated on Intracellular calcium concentration and contracture. Caffeine application to isolated rat ventricular myocytes produced an increase in intracellular calcium and contracture, with the contracture shape depending on application speed and concentration.