For many contractility studies, defined functional states of skinned muscle
fiber preparations can be introduced by application of standardized perfus
ion protocols with large varieties of experimental solutions. Functionally
important subcellular element distributions in the myoplasm and in the sarc
oplasmic reticulum can be measured with high spatial resolution by electron
microscopic microanalysis. Capturing these subcellular ion distributions r
equires their rapid immobilization by quick-freezing. We therefore combined
a plunge-freezing device with a semiautomatic solution exchanger to reprod
ucibly perfuse skinned muscle fiber bundles with multiple solutions. The is
ometric tension produced is simultaneously recorded as an indicator for the
functional state. The samples can be quick-frozen at any chosen time of th
e tension transient. A cryoglueing technique finally delivers specimens sui
table for cryoultramicrotomy.