Ca2+ inhibits outward current through single K+ channels in canine atrial myocyte sarcolemma

Am J Physiol. 1988 Mar;254(3 Pt 1):C397-403. doi: 10.1152/ajpcell.1988.254.3.C397.

Abstract

Single-channel currents in canine atrial cells were recorded by the patch-clamp technique in a bathing solution containing 150 mM [K+] and pipette solutions containing 5 mM [K+]. One kind of current was observed in 56% of 178 cell-free patches and in 3% of 60 patches in the cell-attached configuration. Single-channel amplitude varied in direct proportion to the bath [K+]. Openings of these single channels were prevented when bath [Ca2+] exceeded 1 microM. Below this concentration single-channel percent open time was inversely proportional to log [Ca2+]. Inward current was observed at hyperpolarized membrane potentials in some patches. There was no apparent steady-state voltage sensitivity. These properties suggest that the K+ channel described in this study (gK+LF), a low transition frequency K+ conductor, may be distinct from single K+ channels previously studied in cardiac myocyte sarcolemmae. The single-channel response to "intracellular" free [Ca2+] and the single-channel kinetic characteristics described in this study are similar to the macroscopic "long-lasting transient outward current" (IIO) described by Escande et al. [Am. J. Physiol. 252 (Heart Circ. Physiol. 21): H142-H148, 1987] in human atrial myocytes (tau open = 29.6 ms, tau inactivation = 35.7 ms, respectively). This suggests that gK+LF channels may carry IIO.

Publication types

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

MeSH terms

  • Animals
  • Calcium / pharmacology*
  • Dogs
  • Heart Atria
  • Intracellular Membranes / metabolism
  • Ion Channels / drug effects*
  • Ion Channels / physiology
  • Myocardium / cytology
  • Myocardium / metabolism*
  • Myocardium / ultrastructure
  • Osmolar Concentration
  • Potassium / metabolism*
  • Sarcolemma / metabolism*

Substances

  • Ion Channels
  • Potassium
  • Calcium