Intracellular Na(+) modulates large conductance Ca(2+)-activated K (+) currents in human umbilical vein endothelial cells

Pflugers Arch. 2008 Oct;457(1):67-75. doi: 10.1007/s00424-008-0490-9. Epub 2008 Mar 26.

Abstract

We studied the effects of Na(+) influx on large-conductance Ca(2+)-activated K(+) (BK(Ca)) channels in cultured human umbilical vein endothelial cells (HUVECs) by means of patch clamp and SBFI microfluorescence measurements. In current-clamped HUVECs, extracellular Na(+) replacement by NMDG(+) or mannitol hyperpolarized cells. In voltage-clamped HUVECs, changing membrane potential from 0 mV to negative potentials increased intracellular Na(+) concentration ([Na(+)](i)) and vice versa. In addition, extracellular Na(+) depletion decreased [Na(+)](i). In voltage-clamped cells, BK(Ca) currents were markedly increased by extracellular Na(+) depletion. In inside-out patches, increasing [Na(+)](i) from 0 to 20 or 40 mM reduced single channel conductance but not open probability (NPo) of BK(Ca) channels and decreasing intracellular K(+) concentration ([K(+)](i)) gradually from 140 to 70 mM reduced both single channel conductance and NPo. Furthermore, increasing [Na(+)](i) gradually from 0 to 70 mM, by replacing K(+), markedly reduced single channel conductance and NPo. The Na(+)-Ca(2+) exchange blocker Ni(2+) or KB-R7943 decreased [Na(+)](i) and increased BK(Ca) currents simultaneously, and the Na(+) ionophore monensin completely inhibited BK(Ca) currents. BK(Ca) currents were significantly augmented by increasing extracellular K(+) concentration ([K(+)](o)) from 6 to 12 mM and significantly reduced by decreasing [K(+)](o) from 12 or 6 to 0 mM or applying the Na(+)-K(+) pump inhibitor ouabain. These results suggest that intracellular Na(+) inhibit single channel conductance of BK(Ca) channels and that intracellular K(+) increases single channel conductance and NPo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Electrophysiology
  • Endothelial Cells / drug effects
  • Endothelial Cells / physiology*
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Intracellular Space / metabolism
  • Intracellular Space / physiology
  • Ionophores / pharmacology
  • Large-Conductance Calcium-Activated Potassium Channels / drug effects*
  • Membrane Potentials / physiology
  • Monensin / pharmacology
  • Patch-Clamp Techniques
  • Potassium / metabolism
  • Potassium / pharmacology
  • Sodium / metabolism
  • Sodium / pharmacology*
  • Sodium-Calcium Exchanger / antagonists & inhibitors
  • Sodium-Calcium Exchanger / physiology
  • Sodium-Potassium-Exchanging ATPase / antagonists & inhibitors
  • Sodium-Potassium-Exchanging ATPase / physiology
  • Thiourea / analogs & derivatives
  • Thiourea / pharmacology
  • Umbilical Veins / metabolism
  • Umbilical Veins / physiology*

Substances

  • 2-(2-(4-(4-nitrobenzyloxy)phenyl)ethyl)isothiourea methanesulfonate
  • Enzyme Inhibitors
  • Ionophores
  • Large-Conductance Calcium-Activated Potassium Channels
  • Sodium-Calcium Exchanger
  • Monensin
  • Sodium
  • Sodium-Potassium-Exchanging ATPase
  • Thiourea
  • Potassium