We have performed a comparative study of Ca”+ release rom the sarcoplasmic reticulum (SR) of chemically skinned fibers from rabbit fast- and slow-twitch skeletal muscle. Ca fluxes have been indirectly monitored by following either tension development or the inhibition of net Ca loading rate by a light-scattering method. Several drugs (Ca-release modulators) have been used to either trigger or block Ca2+ release. Our results indicate that caffeine, doxorubicin, and ryanodine activate Ca release, whereas ruthenium red blocks Ca2+ release from both fast- and slow-twitch skinned fibers. Caffeine has greater affinity for slow SR, whereas doxorubicin, ruthenium red, and ryanodine have greater affinity for fast SR. Our results indicate that Ca”+-release mechanisms in fast and slow SR are homologous but not identical and that differences in twitch contraction time might be also related to the inherent properties of the Ca-release mechanism.

Ca2+ release from sarcoplasmic reticulum of skinned fast and slow-twitch muscle fibers

VOLPE, POMPEO
1988

Abstract

We have performed a comparative study of Ca”+ release rom the sarcoplasmic reticulum (SR) of chemically skinned fibers from rabbit fast- and slow-twitch skeletal muscle. Ca fluxes have been indirectly monitored by following either tension development or the inhibition of net Ca loading rate by a light-scattering method. Several drugs (Ca-release modulators) have been used to either trigger or block Ca2+ release. Our results indicate that caffeine, doxorubicin, and ryanodine activate Ca release, whereas ruthenium red blocks Ca2+ release from both fast- and slow-twitch skinned fibers. Caffeine has greater affinity for slow SR, whereas doxorubicin, ruthenium red, and ryanodine have greater affinity for fast SR. Our results indicate that Ca”+-release mechanisms in fast and slow SR are homologous but not identical and that differences in twitch contraction time might be also related to the inherent properties of the Ca-release mechanism.
1988
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/105680
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