Effects of U-83836E on glutamate-induced neurotoxicity in dissociated rat cerebellar granule cells

Toxicol Appl Pharmacol. 1999 Apr 1;156(1):1-5. doi: 10.1006/taap.1998.8613.

Abstract

The effects of the lazaroid compound U-83836E on the glutamate-induced production of reactive oxygen species (ROS) were studied in dissociated rat cerebellar granule cells by flow cytometry. U-83836E completely inhibited ROS production with an estimated IC50 value of 21.7 +/- 9.1 nM. However, U-83836E did not inhibit the glutamate-evoked decrease in mitochondrial membrane potential (MMP). Nevertheless, U-83836E (10 nM to 10 microM) prevented cell death induced by 10 mM of glutamate. At concentrations above 10 microM, U-83836E by itself showed slight cytotoxicity, which was significant at a 100 microM concentration. U-83836E (25 to 200 microM) also increased the cytosolic calcium levels in a concentration-dependent manner. Our results indicate that the cytotoxic effects found at micromolar concentrations of U-83836E could be explained by an increase in [Ca2+]i. Finally, since U-83836E did not prevent the MMP decrease evoked by glutamate, it is suggested that antioxidant pharmacotherapy would not be sufficient to block the neurotoxic effects of glutamate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology*
  • Calcium / metabolism
  • Cell Survival / drug effects
  • Cerebellum / drug effects*
  • Cerebellum / metabolism
  • Chromans / pharmacology*
  • Glutamic Acid / toxicity*
  • Membrane Potentials / drug effects
  • Neuroprotective Agents / pharmacology*
  • Piperazines / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species / metabolism

Substances

  • Antioxidants
  • Chromans
  • Neuroprotective Agents
  • Piperazines
  • Reactive Oxygen Species
  • U 78517F
  • Glutamic Acid
  • Calcium