Mechanism of Ivermectin Facilitation of Human P2X4 Receptor Channels

Avi Priel, Shai D. Silberberg

Research output: Contribution to journalArticlepeer-review

148 Scopus citations

Abstract

Ivermectin (IVM), a widely used antiparasitic agent in human and veterinary medicine, was recently shown to augment macroscopic currents through rat P2X4 receptor channels (Khakh, B.S., W.R. Proctor, T.V. Dunwiddie, C. Labarca, and H.A. Lester. 1999. J. Neurosci. 19:7289-7299.). In the present study, the effects of IVM on the human P2X4 (hP2X 4) receptor channel stably transfected in HEK293 cells were investigated by recording membrane currents using the patch clamp technique. In whole-cell recordings, IVM (≤10 μM) applied from outside the cell (but not from inside) increased the maximum current activated by ATP, and slowed the rate of current deactivation. These two phenomena likely result from the binding of IVM to separate sites. A higher affinity site (EC50 0.25 μM) increased the maximal current activated by saturating concentrations of ATP without significantly changing the rate of current deactivation or the EC50 and Hill slope of the ATP concentration-response relationship. A lower affinity site (EC50 2 μM) slowed the rate of current deactivation, and increased the apparent affinity for ATP. In cell-attached patch recordings, P2X4 receptor channels exhibited complex kinetics, with multiple components in both the open and shut distributions. IVM (0.3 μM) increased the number of openings per burst, without significantly changing the mean open or mean shut time within a burst. At higher concentrations (1.5 μM) of IVM, two additional open time components of long duration were observed that gave rise to long-lasting bursts of channel activity. Together, the results suggest that the binding of IVM to the higher affinity site increases current amplitude by reducing channel desensitization, whereas the binding of IVM to the lower affinity site slows the deactivation of the current predominantly by stabilizing the open conformation of the channel.

Original languageEnglish
Pages (from-to)281-293
Number of pages13
JournalJournal of General Physiology
Volume123
Issue number3
DOIs
StatePublished - 1 Mar 2004

Keywords

  • ATP
  • Allosteric regulation
  • Ion channel gating
  • Patch clamp techniques
  • Purinergic receptors

ASJC Scopus subject areas

  • Physiology

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