The effects of 100 mu M ryanodine on the L-type calcium channel were s
tudied using the pacth-clamp technique in isolated guinea pig ventricu
lar myocytes. The inactivation kinetics of the calcium current were sl
owed down in the presence of ryanodine in agreement with the blockade
of the release of calcium from the sarcoplasmic reticulum by the drug.
The I-V and steady-state inactivation curves of the calcium current w
ere shifted to negative values by ryanodine. A similar shift was obser
ved in the activation and inactivation curves of the intramembrane cha
rge movement associated with the calcium channel. Due to this shift, r
yanodine slightly reduced the maximal amount of displaced charge altho
ugh it did not modify the transition from the inactivated to the activ
ated state (i.e., charge movement repriming). This result is in notabl
e contrast with that obtained in skeletal muscle, where it has been fo
und that ryanodine interferes with charge movement repriming. These re
sults provide additional evidence of the postulated differences betwee
n the architecture of the excitation-contraction coupling system in ca
rdiac and skeletal muscle.