Potassium channels in cardiac cells activated by arachidonic acid and phospholipids

Science. 1989 Jun 9;244(4909):1174-6. doi: 10.1126/science.2727703.

Abstract

Two types of potassium-selective channels activated by intracellular arachidonic acid or phosphatidylcholine have been found in neonatal rat atrial cells. In inside-out patches, arachidonic acid and phosphatidylcholine each opened outwardly rectifying potassium-selective channels with conductances of 160 picosiemens (IK.AA) and 68 picosiemens (IK.PC), respectively. These potassium channels were not sensitive to internally applied adenosine triphosphate (ATP), magnesium, or calcium. Lowering the intracellular pH from 7.2 to 6.8 or 6.4 reversibly increased IK.AA channel activity three- or tenfold, respectively. A number of fatty acid derivatives were tested for their ability to activate IK.AA. These potassium-selective channels may help explain the increase in potassium conductance observed in ischemic cells and raise the possibility that fatty acid derivatives act as second messengers.

Publication types

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

MeSH terms

  • Animals
  • Animals, Newborn
  • Arachidonic Acids / pharmacology*
  • Atrial Function
  • Heart / physiology*
  • Hydrogen-Ion Concentration
  • In Vitro Techniques
  • Kinetics
  • Membrane Potentials
  • Phosphatidylcholines / pharmacology*
  • Potassium Channels / drug effects
  • Potassium Channels / physiology*
  • Rats

Substances

  • Arachidonic Acids
  • Phosphatidylcholines
  • Potassium Channels