Activation of chloride current by purinergic stimulation in guinea pig heart cells

Circ Res. 1992 Apr;70(4):851-5. doi: 10.1161/01.res.70.4.851.

Abstract

Single atrial cells from guinea pig heart were voltage-clamped using the whole-cell configuration of the patch-clamp technique under conditions in which most of the ionic and exchange currents known in cardiac cells were minimized. Extracellular 5 or 50 microM ATP activated a Cl- current, in addition to a rapidly desensitizing cation-selective current. A nonhydrolyzable ATP analogue, adenosine-5'-O-(3-thiotriphosphate) (50 microM), also evoked these two currents, indicating involvement of purinoceptors rather than ecto-ATPase on the membrane. ADP, AMP, and adenosine were also effective in inducing the Cl- current, showing no clear order of potency for the purinoceptor subtypes involved. The purinoceptor-activated Cl- current, like the beta-catecholamine-cAMP-dependent cardiac Cl- current, showed outward rectification and time independence.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine Nucleotides / pharmacology
  • Adenosine / pharmacology
  • Adenosine Triphosphate / pharmacology
  • Animals
  • Chloride Channels
  • Chlorides / physiology*
  • Cytological Techniques
  • Guinea Pigs
  • Heart / drug effects
  • Heart / physiology*
  • In Vitro Techniques
  • Ion Channels / drug effects*
  • Ion Channels / physiology
  • Membrane Proteins / drug effects*
  • Membrane Proteins / physiology
  • Myocardium / cytology*
  • Receptors, Purinergic / drug effects*
  • Stimulation, Chemical

Substances

  • Adenine Nucleotides
  • Chloride Channels
  • Chlorides
  • Ion Channels
  • Membrane Proteins
  • Receptors, Purinergic
  • Adenosine Triphosphate
  • Adenosine