Cocaine binds to a common site on open and inactivated human heart (Nav 1.5) sodium channels

M. E. O'Leary, M. Chahine

Research output: Contribution to journalArticlepeer-review

48 Scopus citations

Abstract

The inhibition by cocaine of the human heart Na+ channel (Nav1.5) heterologously expressed in Xenopus oocytes was investigated. Cocaine produced little tonic block of the resting channels but induced a characteristic, use-dependent inhibition during rapid, repetitive stimulation, suggesting that the drug preferentially binds to the open or inactivated states of the channel. To investigate further the state dependence, depolarizing pulses were used to inactivate the channels and promote cocaine binding. Cocaine produced a slow, concentration-dependent inhibition of inactivated channels, which had an apparent KD of 3.4 μM. Mutations of the interdomain III-IV linker that remove fast inactivation selectively abolished this high-affinity component of cocaine inhibition, which appeared to be linked to the fast inactivation of the channels. A rapid component of cocaine inhibition persisted in the inactivation-deficient mutant that was enhanced by depolarization and was sensitive to changes in the concentration of external Na+, properties that are consistent with a pore-blocking mechanism. Cocaine induced a use-dependent inhibition of the non-inactivating mutant and delayed the repriming at hyperpolarized voltages, indicating that the drug slowly dissociated when the channels were closed. Mutation of a conserved aromatic residue (Y1767) of the D4S6 segment weakened both the inactivation-dependent and the pore-blocking components of the cocaine inhibition. The data indicate that cocaine binds to a common site located within the internal vestibule and inhibits cardiac Na+ channels by blocking the pore and by stabilizing the channels in an inactivated state.

Original languageEnglish (US)
Pages (from-to)701-716
Number of pages16
JournalJournal of Physiology
Volume541
Issue number3
DOIs
StatePublished - Jun 15 2002
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Physiology

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