Trimethyltin and triethyltin differentially induce spontaneous noradrenaline release from rat hippocampal slices

Toxicol Appl Pharmacol. 2000 Feb 1;162(3):189-96. doi: 10.1006/taap.1999.8845.

Abstract

The environmental contaminants trimethyltin (TMT) and triethyltin (TET) stimulated the spontaneous release of [(3)H]noradrenaline ([(3)H]NA) from hippocampal slices in a time- and concentration-dependent manner. TMT was the most potent compound, exhibiting an EC50 value 10-fold lower (3.8 microM) than that of TET (39.5 microM). Metal-evoked [(3)H]NA release did not increase in the absence of desipramine and was completely blocked by reserpine preincubation, indicating a vesicular origin of [(3)H]NA release but not a mechanism involving reversal of the transmitter transporter. The voltage-gated Na(+) channel blocker tetrodotoxin (TTX) did not affect metal-evoked [(3)H]NA release. [(3)H]NA release elicited by TMT was partially extracellular Ca(2+)-dependent, since it was significantly decreased in a Ca(2+)-free EGTA-containing medium, whereas TET induced an extracellular Ca(2+)-independent release of [(3)H]NA. Neither inhibitors of Ca(2+)-entry through Na(+)/Ca(2+)exchanger and voltage-gated calcium channels, nor agents that interfere with Ca(2+)-mobilization from intracellular stores affected [(3)H]NA release induced by TMT. TET-evoked [(3)H]NA release was reduced by ruthenium red, which depletes mitochondrial Ca(2+)stores, but was not modified by caffeine and thapsigargin, which interfere with Ca(2+)mobilization from endoplasmic reticulum. The fact that TET effect was also attenuated by DIDS, an inhibitor of anion exchange, indicates that the effect of TET on spontaneous [(3)H]NA release may be mediated by intracellular mobilization of Ca(2+) from mitochondrial stores through a Cl(-) dependent mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid / pharmacology
  • Adrenergic Uptake Inhibitors / pharmacology
  • Animals
  • Biological Transport / drug effects
  • Calcium / metabolism
  • Calcium Channel Blockers / pharmacology
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Chelating Agents / pharmacology
  • Chlorides / metabolism
  • Desipramine / pharmacology
  • Egtazic Acid / pharmacology
  • Environmental Pollutants / toxicity
  • Hippocampus / drug effects*
  • Hippocampus / metabolism*
  • Ions
  • Male
  • Norepinephrine / antagonists & inhibitors
  • Norepinephrine / metabolism*
  • Rats
  • Rats, Wistar
  • Sodium / metabolism
  • Sodium Channel Blockers
  • Sodium Channels / metabolism
  • Sodium-Calcium Exchanger / antagonists & inhibitors
  • Sodium-Calcium Exchanger / metabolism
  • Tetrodotoxin / pharmacology
  • Triethyltin Compounds / toxicity*
  • Trimethyltin Compounds / toxicity*
  • Tritium
  • omega-Conotoxin GVIA / pharmacology

Substances

  • Adrenergic Uptake Inhibitors
  • Calcium Channel Blockers
  • Chelating Agents
  • Chlorides
  • Environmental Pollutants
  • Ions
  • Sodium Channel Blockers
  • Sodium Channels
  • Sodium-Calcium Exchanger
  • Triethyltin Compounds
  • Trimethyltin Compounds
  • Tritium
  • trimethyltin
  • Tetrodotoxin
  • Egtazic Acid
  • triethyltin
  • omega-Conotoxin GVIA
  • Sodium
  • 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid
  • Calcium
  • Desipramine
  • Norepinephrine