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Vol. 281, Issue 1, 84-92, 1997
Center for Biomedical Physics, Temple University Medical School,
Philadelphia, Pennsylvania
The effects of short-chain alcohols (methanol, ethanol and
n-propanol) on the fast-inactivating, A-type, potassium
current of Lymnaea neurons were examined using
macroscopic recording techniques. Alcohols produced a blockade of the
current and modified its inactivation mechanism. The extracellular
concentrations of methanol, ethanol and n-propanol
causing 50% suppression of the current were 2970, 830 and 230 mM,
respectively. The main effects of alcohols on inactivation were a
decrease in the amplitude of the fast component and a simultaneous
increase in the amplitude of the slow component of inactivation. In a
model, the suppression of the fast component could be reproduced by an
increase of the backward rate constant related to the dissociation of
the inactivation particle from its binding site. The blockade and
modification of inactivation reveal similar dependences on ethanol
concentration, indicating that the same type of interaction of ethanol
with the channel underlies both of these events. Ethanol was effective
only in extracellular applications. The data support an action of
alcohols at a hydrophobic site near the extracellular portion of the
channel.