Effects of divalent cations on single-channel conduction properties of Xenopus IP3 receptor

Am J Physiol. 1998 Jul;275(1):C179-88. doi: 10.1152/ajpcell.1998.275.1.C179.

Abstract

The effects of Mg2+ and Ba2+ on single-channel properties of the inositol 1,4,5-trisphosphate receptor (IP3R) were studied by patch clamp of isolated nuclei from Xenopus oocytes. In 140 mM K+ the IP3R channel kinetics and presence of conductance substates were similar over a range (0-9.5 mM) of free Mg2+. In 0 mM Mg2+ the channel current-voltage (I-V) relation was linear with conductance of approximately 320 pS. Conductance varied slowly and continuously over a wide range (SD approximately 60 pS) and sometimes fluctuated during single openings. The presence of Mg2+ on either or both sides of the channel reduced the current (blocking constant approximately 0.6 mM in symmetrical Mg2+), as well as the range of conductances observed, and made the I-V relation nonlinear (slope conductance approximately 120 pS near 0 mV and approximately 360 pS at +/-70 mV in symmetrical 2.5 mM Mg2+). Ba2+ exhibited similar effects on channel conductance. Mg2+ and Ba2+ permeated the channel with a ratio of permeability of Ba2+ to Mg2+ to K+ of 3.5:2.6:1. These results indicate that divalent cations induce nonlinearity in the I-V relation and reduce current by a mechanism involving permeation block of the IP3R due to strong binding to site(s) in the conduction pathway. Furthermore, stabilization of conductance by divalent cations reveals a novel interaction between the cations and the IP3R.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Barium / pharmacology*
  • Calcium Channels / drug effects
  • Calcium Channels / physiology*
  • Cations, Divalent / pharmacology*
  • Electric Conductivity
  • Female
  • Inositol 1,4,5-Trisphosphate / physiology
  • Inositol 1,4,5-Trisphosphate Receptors
  • Kinetics
  • Magnesium / pharmacology*
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Oocytes / drug effects
  • Oocytes / physiology*
  • Potassium / pharmacology
  • Reaction Time
  • Receptors, Cytoplasmic and Nuclear / drug effects
  • Receptors, Cytoplasmic and Nuclear / physiology*
  • Xenopus laevis

Substances

  • Calcium Channels
  • Cations, Divalent
  • Inositol 1,4,5-Trisphosphate Receptors
  • Receptors, Cytoplasmic and Nuclear
  • Barium
  • Inositol 1,4,5-Trisphosphate
  • Magnesium
  • Potassium