Hypotonicity and ethanol modulate BK channel activity and chloride currents in GH4/C1 pituitary tumour cells

Acta Physiol (Oxf). 2006 May-Jun;187(1-2):51-9. doi: 10.1111/j.1748-1716.2006.01544.x.

Abstract

Aim: Description of the effects of hypotonic cell swelling and ethanol on maxi Ca2+-activated K+ channel (BK channel) activity and Cl- channel activity in GH4/C1 pituitary tumour cells.

Methods: Whole cell-, cell attached- and outside-out patch clamp measurements, fluorescence (fluo-3) measurements of intracellular Ca2+ concentration, cell size video monitoring.

Results: GH4/C1 pituitary tumour cells respond to both hypotonicity and ethanol with cell swelling which is followed by a regulatory volume decrease (RVD). Tetraethylammonium and 4,4'-diisothiocyanatostilbene-2,2'-disulphonic acid (DIDS) induced cell swelling per se and inhibited hypotonicity induced RVD. Ethanol-induced swelling is paralleled by an increase in the intracellular Ca2+ concentration and augmented by DIDS. BK channel activation by hypotonicity and ethanol is demonstrated in patch clamp experiments both in intact cells (cell attached configuration) and a subset of excised membrane patches (outside-out configuration). Cell swelling and addition of ionomycin under isotonic conditions leads to the activation of outwardly rectifying Cl- currents with time dependent activation at positive potentials.

Conclusions: In GH4/C1 cells both hypotonicity and ethanol lead to cell swelling, RVD and to activation of BK channels. The hypotonicity-induced BK channel activation can also be observed in cell free outside-out patches. Hypotonicity, but not ethanol leads to the activation of Cl- channels with features of Ca2+-activated Cl- currents.

Publication types

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

MeSH terms

  • 3T3 Cells
  • 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid / pharmacology
  • Animals
  • Calcium / metabolism
  • Cell Line, Tumor
  • Cell Membrane / metabolism
  • Cell Size
  • Central Nervous System Depressants / pharmacology*
  • Chloride Channels / metabolism*
  • Ethanol / pharmacology*
  • Humans
  • Hypotonic Solutions / pharmacology*
  • Mice
  • Microscopy, Video
  • Patch-Clamp Techniques
  • Pituitary Neoplasms / metabolism*
  • Potassium Channel Blockers / pharmacology
  • Potassium Channels / metabolism
  • Tetraethylammonium / pharmacology

Substances

  • Central Nervous System Depressants
  • Chloride Channels
  • Hypotonic Solutions
  • Potassium Channel Blockers
  • Potassium Channels
  • Ethanol
  • Tetraethylammonium
  • 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid
  • Calcium