Abstract
1. Muscarinic K+ current (IK(ACh)) elicited by acetylcholine (ACh)
was measured in guinea-pig atrial myocytes, which were either freshly
isolated or cultured for up to 8 days. 2. The half-time of activation
of inward IK(ACh) by a saturating concentration (10 microM) of ACh
decreased from approximately 400 ms (in freshly isolated cells) to
250 ms after 6 days in culture. This was paralleled by an increase
in the fast desensitizing component of IK(ACh). The density of steady-state
currents was not changed. Downregulation of M2 receptors by long-term
treatment of isolated myocytes with carbachol in vitro had opposite
effects. 3. The EC50 of ACh for the activation of steady-state IK(ACh)
was reduced from 5 x 10(-7) M (day 0) to 8 x 10(-8) M (day 6). The
shift in EC50 occurred with a half-time of about 2 days, similar
to the recovery from downregulation induced by treating atrial myocytes
with carbachol in vitro. 4. The increase in sensitivity to ACh can
be accounted for by an approximately 6-fold increase in the density
of M2 receptors. 5. It is concluded that sensitization in culture
reflects recovery from downregulation of M2 receptors due to the
tonic vagal input to the heart in the intact animal.
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