Abstract
It is now thought that amine local anaesthetic compounds (procaine, lignocaine and related molecules) depress electrical activity in nerve and muscle cells by binding to sites within ion channels and blocking current flow. Such mechanisms have been proposed to account for the effects of these local anaesthetics on both the voltage-dependent sodium current1–3 and the post-synaptic acetylcholine (ACh)-activated ionic current4–7. Recently, strong evidence for block of ion channels by cationic drug molecules has been obtained by recording current from single ACh-activated channels in the presence of permanently charged quaternary derivatives of lignocaine8. Most amine local anaesthetic compounds are, however, weak bases, present in both charged and uncharged forms at physiological pH, and some question remains as to whether a charged group is essential for blockade of ion channels1,9,10. To resolve this question, we studied the action of the uncharged local anaesthetic benzocaine (ethyl-4-aminobenzoate) on postsynaptic ACh- activated end-plate current and extrajunctional single channel current of frog muscle. We report here evidence that strongly suggests that benzocaine blocks ACh-activated ion channels.
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Ogden, D., Siegelbaum, S. & Colquhoun, D. Block of acetylcholine-activated ion channels by an uncharged local anaesthetic. Nature 289, 596–598 (1981). https://doi.org/10.1038/289596a0
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DOI: https://doi.org/10.1038/289596a0
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