Rat cerebellar granule cells are protected from glutamate-induced excitotoxicity by S-nitrosoglutathione but not glutathione

Am J Physiol Cell Physiol. 2004 Apr;286(4):C893-904. doi: 10.1152/ajpcell.00127.2003.

Abstract

In cultured rat cerebellar granule cells, glutamate or N-methyl-d-aspartate (NMDA) activation of the NMDA receptor caused a sustained increase in cytosolic Ca(2+) levels ([Ca(2+)](i)), reactive oxygen species (ROS) generation, and cell death (respective EC(50) values for glutamate were 12, 30, and 38 microM) but no increase in caspase-3 activity. Removal of extracellular Ca(2+) blocked all three glutamate-induced effects, whereas pretreatment with an ROS scavenger inhibited glutamate-induced cell death but had no effect on the [Ca(2+)](i) increase. This indicates that glutamate-induced cell death is attributable to [Ca(2+)](i) increase and ROS generation, and the [Ca(2+)](i) increase precedes ROS generation. Apoptotic cell death was not seen until 24 h after exposure of cells to glutamate. S-nitrosoglutathione abolished glutamate-induced ROS generation and cell death, and only a transient [Ca(2+)](i) increase was seen; similar results were observed with another nitric oxide (NO) donor, S-nitroso-N-acetylpenicillamine, but not with glutathione, which suggests that the effects were caused by NO. The transient [Ca(2+)](i) increase and the abolishment of ROS generation induced by glutamate and S-nitrosoglutathione were still seen in the presence of an ROS scavenger. Glial cells, which were present in the cultures used, showed no [Ca(2+)](i) increase in the presence of glutamate, and glutamate-induced granule cell death was independent of the percentage of glial cells. In conclusion, NO donors protect cultured cerebellar granule cells from glutamate-induced cell death, which is mediated by ROS generated by a sustained [Ca(2+)](i) increase, and glial cells provide negligible protection against glutamate-induced excitotoxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone / pharmacology
  • Cells, Cultured
  • Cerebellum / cytology
  • Enzyme Inhibitors / pharmacology
  • Excitatory Amino Acid Antagonists / pharmacology
  • Glutamic Acid / toxicity*
  • Glutathione / pharmacology*
  • Glycine / pharmacology
  • Ionophores / pharmacology
  • Magnesium / pharmacology
  • Neurons / cytology
  • Neurons / drug effects*
  • Neurons / physiology*
  • Neuroprotective Agents / pharmacology*
  • Neurotoxins / pharmacology
  • Nitric Oxide / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species / metabolism
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • S-Nitrosoglutathione / pharmacology*
  • Thapsigargin / pharmacology

Substances

  • Enzyme Inhibitors
  • Excitatory Amino Acid Antagonists
  • Ionophores
  • Neuroprotective Agents
  • Neurotoxins
  • Reactive Oxygen Species
  • Receptors, N-Methyl-D-Aspartate
  • Nitric Oxide
  • Glutamic Acid
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone
  • S-Nitrosoglutathione
  • Thapsigargin
  • Glutathione
  • Magnesium
  • Glycine