Chloroquine blocks the Kir4.1 channels by an open-pore blocking mechanism

Eur J Pharmacol. 2017 Apr 5;800:40-47. doi: 10.1016/j.ejphar.2017.02.024. Epub 2017 Feb 20.

Abstract

Kir4.1 channels have been implicated in various physiological processes, mainly in the K+ homeostasis of the central nervous system and in the control of glial function and neuronal excitability. Even though, pharmacological research of these channels is very limited. Chloroquine (CQ) is an amino quinolone derivative known to inhibit Kir2.1 and Kir6.2 channels with different action mechanism and binding site. Here, we employed patch-clamp methods, mutagenesis analysis, and molecular modeling to characterize the molecular pharmacology of Kir4.1 inhibition by CQ. We found that this drug inhibits Kir4.1 channels heterologously expressed in HEK-293 cells. CQ produced a fast-onset voltage-dependent pore-blocking effect on these channels. In inside-out patches, CQ showed notable higher potency (IC50 ≈0.5μM at +50mV) and faster onset of block when compared to whole-cell configuration (IC50 ≈7μM at +60mV). Also, CQ showed a voltage-dependent unblock with repolarization. These results suggest that the drug directly blocks Kir4.1 channels by a pore-plugging mechanism. Moreover, we found that two residues (Thr128 and Glu158), facing the central cavity and located within the transmembrane pore, are particularly important structural determinants of CQ block. This evidence was similar to what was previously reported with Kir6.2, but distinct from the interaction site (cytoplasmic pore) CQ-Kir2.1. Thus, our findings highlight the diversity of interaction sites and mechanisms that underlie amino quinolone inhibition of Kir channels.

Keywords: Cationic amphiphilic drugs; Chloroquine; Kir4.1 channels.

MeSH terms

  • Binding Sites
  • Chloroquine / metabolism
  • Chloroquine / pharmacology*
  • Cytoplasm / drug effects
  • Cytoplasm / metabolism
  • HEK293 Cells
  • Humans
  • Ion Channel Gating / drug effects
  • Kinetics
  • Molecular Docking Simulation
  • Porosity
  • Potassium Channel Blockers / metabolism
  • Potassium Channel Blockers / pharmacology*
  • Potassium Channels, Inwardly Rectifying / antagonists & inhibitors*
  • Potassium Channels, Inwardly Rectifying / chemistry*
  • Potassium Channels, Inwardly Rectifying / metabolism
  • Protein Conformation

Substances

  • Kcnj10 (channel)
  • Potassium Channel Blockers
  • Potassium Channels, Inwardly Rectifying
  • Chloroquine