Abstract
According to Hille’s modulated receptor hypothesis, benzocaine shares a common receptor with all other local anesthetics (LAs) in the voltage-gated Na+ channel. We tested this single receptor hypothesis using mutant muscle Na+ channels of μ1-I1575A, F1579A, and N1584A transiently expressed in Hek-293t cells. Both benzocaine and etidocaine are more effective at blocking μ1-N1584A current than the wild-type current, while they are less potent at blocking μ1-F1579A current. Such concurrent changes of both benzocaine and etidocaine potency towards F1579A and N1584A mutants suggest that they share a common LA receptor. Consistent with results found in studies of native Na+ channels, permanently charged QX-314 at 1 mM is not effective at blocking wild-type, F1579A, and N1584A current via external application. In contrast, QX-314 is relatively potent at blocking I1575A current when applied externally. This increased potency of external QX-314 against the μ1-I1575A mutant has been reported previously in a study of the brain counterpart. Mutant I1575A also appears to be highly sensitive to the external divalent cation Cd2+, probably because of the presence of cysteine residues near the μ1-I1575 position in the IV-S6 segment. To our surprise, neutral benzocaine becomes more effective at blocking μ1-I1575A current than the wild-type current, whereas the opposite is found for etidocaine. We hypothesize that an increase in accessibility of external QX-314 to the μ1-I1575A mutant is accompanied by a reduction of binding towards the charged amine component.
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Received: 27 May 1997 / Received after revision: 29 August 1997 / Accepted: 5 September 1997
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Wang, G., Quan, C. & Wang, SY. A common local anesthetic receptor for benzocaine and etidocaine in voltage-gated μ1 Na+ channels. Pflügers Arch 435, 293–302 (1997). https://doi.org/10.1007/s004240050515
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DOI: https://doi.org/10.1007/s004240050515