S. Koumi et al., BETA-ADRENERGIC AND CHOLINERGIC MODULATION OF INWARD RECTIFIER K-PIG VENTRICLE( CHANNEL FUNCTION AND PHOSPHORYLATION IN GUINEA), Journal of physiology, 486(3), 1995, pp. 661-678
1. To clarify the nature of the inhibition of whole-cell inwardly rect
ifying K+ current (I-k1) by isoprenaline (Iso) and its antagonism by a
cetylcholine (ACh), we studied the effects of Iso and ACh and their su
rrogates on single channel currents (i(k1)) carried by inwardly rectif
ying K+ channels in cell-attached and excised inside-out patches obtai
ned from guinea-pig ventricular myocytes. 2. Bath application of Iso s
uppressed i(K1) channel activity in cell-attached patches. This was in
hibited by propranolol. Bath-applied forskolin or dibutyryl cAMP mimic
ked the effect of bath-applied Iso. 3. Exposure of the cytosolic face
of inside-out patches to purified catalytic subunit of the cAMP-depend
ent protein kinase (PKA) also suppressed i(K1) channel activity, mimic
king the effect of bath-applied Iso on i(K1) recorded from cell-attach
ed patches. 4. When applied directly to cell-attached patches via the
patch pipette solution, ACh antagonized Iso-induced (1 mu M applied vi
a the bath) suppression of i(K1) channels. In contrast, bath-applied A
Ch(10 mu M) partially antagonized the effect of low concentrations of
Iso (e.g. < 50 nM) on i(K1) channels in cell-attached patches but had
no detectable effect when 1 mu M or more Iso was used. 5. In myocytes
pretreated with pertussis toxin (PTX), ACh failed to antagonize Iso-in
duced suppression of i(K1) channels. When inside-out patches were used
, bath-applied preactivated exogenous inhibitory G protein subunit, G(
1 alpha) antagonized the suppression of i(K1) channels induced by bath
-applied catalytic subunit of PKA (PKA-CX), suggesting that a PTX-sens
itive G(i alpha) mediates ACh-induced antagonism of Iso-induced suppre
ssion of i(K1). 6. Neither GTP gamma S nor G(i alpha) antagonized the
suppression of i(K1) produced by bath-applied PKA-CX in inside-out pat
ches when okadaic acid was present in the bath. In addition, bath appl
ication of alkaline phosphatase also reactivated i(K1) channels suppre
ssed by PXA-CS. 7. Findings in guinea-pig ventricular myocytes suggest
that i(K1) can be suppressed by a PKA-mediated phosphorylation of the
i(K1) channel occurring in response to Iso-induced beta-adrenergic re
ceptor activation and that ACh can antagonize the suppression by mecha
nisms that involve both intracellular and membrane-delimited pathways.
The membrane-delimited pathway appears to involve M(2)-cholinergic re
ceptors, their associated G protein, G(1), and a protein phosphatase,
all located in the sarcolemma in close proximity to the involved i(K1)
channels.