Acetylcholine regulation of nicotinic receptor channels through a putative G protein in chick myotubes.

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Abstract
1. Single-channel currents induced by acetylcholine (ACh) were recorded from unstriated and non-innervated embryonic chick myotubes using the cell-attached patch-clamp technique. 2. ACh applied to the non-patched membrane decreased both channel opening probability and conductance. These ACh-induced effects occurred also when the nonpatched membrane was exposed to nominally Ca2+-free extracellular medium, but were absent when it was treated with curare. 3. ACh-induced membrane current recorded under whole-cell patch-clamp conditions decreased in amplitude and time course when myotubes were intracellularly loaded with guanosine-5''-O-(3-thiotriphosphate) GTP.gamma.S, but not with guanosine-5''-O-(2-thiodiphosphate) (GDP.beta.S) or cyclic adenosine-5''-monophosphate (cyclic AMP). Internal perfusion of GTP.gamma.S affected the ACh-induced openings in a similar manner to the non-patch ACh application. 4. These results suggest that ACh, in addition to its direct effect, acts indirectly on the nicotinic receptor channels by delivering an intracellular messenger and through the activation of a putative G protein.