GTP gamma S causes contraction of skinned frog skeletal muscle via the DHP-sensitive Ca2+ channels of sealed T-tubules.

Abstract

We have investigated the involvement of G-proteins in excitation-contraction coupling of fast-twitch skeletal muscle, using a fibre preparation designed to retain intact T-tubules and sarcoplasmic reticulum. The nonhydrolysable analogue of guanosine triphosphate, GTP gamma S (50-500 microM) caused a strong, transient isometric contraction in this preparation. Reduction of ethylene-bis(oxonitrilo)tetraacete (EGTA) in the sealed T-tubules from 5 mM to 0.1 mM lowered the threshold to GTP gamma S and removal of sodium reversibly raised it. The dihydropyridine (DHP) calcium channel antagonists nicardipine and nifedipine allowed a first contraction and then blocked subsequent GTP gamma S action. The phenylalkylamine methoxyverapamil (D-600) did likewise, reversibly, at 10 degrees C. The guanosine diphosphate analogue, GDP beta S, and procaine reversibly blocked the action of GTP gamma S; pertussis toxin also blocked it. Photolytic release of 40-100 microM GTP gamma S within 0.1 s from S-caged GTP gamma S caused contraction after a latent period of 0.3-20 s. We conclude that GTP gamma S can activate contraction in frog skeletal muscle via a route requiring both the integrity of the T-tubular DHP-sensitive calcium channel (DHPr) and the presence of sodium in the sealed T-tubules. We propose that in this preparation GTP gamma S activates a G-protein, which in turn activates the DHPr as a calcium channel and releases stored calcium from within the sealed T-tubule. Implications of these results for the excitation-contraction coupling mechanism in skeletal muscle are discussed.