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Effect of Adenosine and Intracellular GTP on KATP Channels of Mammalian Skeletal Muscle

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Abstract.

We investigated the action of adenosine and GTP on KATP channels, using inside-out patch clamp recordings from dissociated single fibers of rat flexor digitorum brevis (FDB) skeletal muscle. In excised patches, KATP channels could be activated by a combination of an extracellular adenosine agonist and intracellular Mg2+-ATP and GTP or GTP-γ-S. The activation required hydrolyzable ATP and could be partially reversed with Mg2+, suggesting that it may involve a G-protein dependent phosphorylation of KATP channels. We found that KATP channels of the rat FDB could not be activated by Mg2+-ATP alone or by Mg2+-ATP in the presence of extracellular adenosine. Patches whose channel activity had been `rundown' by Ca2+ could not be recovered by adenosine, GTP or Mg2+-ATP. KATP channels activated by adenosine receptor agonists had a similar ATP sensitivity to those under control conditions; but adenosine appears to be able to switch these KATP channels from an inactive to an active mode.

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Received: 29 December 1995/Revised: 22 March 1996

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Barrett-Jolley, R., Comtois, A., Davies, N. et al. Effect of Adenosine and Intracellular GTP on KATP Channels of Mammalian Skeletal Muscle. J. Membrane Biol. 152, 111–116 (1996). https://doi.org/10.1007/s002329900090

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  • DOI: https://doi.org/10.1007/s002329900090

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