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Cellular and subcellular calcium accumulation during glutamate‐induced injury in cerebellar granule neurons
Author(s) -
Ward Manus W.,
Kushnareva Yulia,
Greenwood Sam,
Connolly Christopher N.
Publication year - 2005
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2004.02928.x
Subject(s) - glutamate receptor , kainate receptor , cerebellum , nmda receptor , excitatory postsynaptic potential , mitochondrion , glutamic acid , biology , neuroscience , chemistry , microbiology and biotechnology , biophysics , biochemistry , ampa receptor , receptor , inhibitory postsynaptic potential , amino acid
We have investigated the role of Ca 2+ accumulation and neuronal injury in cerebellar granule neurons after glutamate receptor overactivation. After the removal of the free cytosolic Ca 2+ we identified an extensive second Ca 2+ fraction (SCF) that is retained within the neurons after glutamate receptor overactivation. The SCF reaches a plateau within 10 min with the magnitude of this SCF accumulation reflecting the extent of the neuronal injury that occurs within the neurons. The existence of this SCF is sensitive to both NMDA receptor antagonists and mitochondrial inhibitors but is unaffected by agents that deplete endoplasmic reticulum Ca 2+ , indicating that this Ca 2+ fraction may be located within the mitochondria. Through the isolation of mitochondria from cerebellar granule neurons treated with glutamate we have shown that the majority of the SCF is mitochondrial in location. On the removal of the glutamate stimulus the SCF recovers at a slower rate than the free Ca 2+ concentration within the neuron. This is intriguing, as it implies a capacity to remember previous excitatory events. Most significantly we have shown that a short pre‐application of subthreshold glutamate or kainate blocks both SCF Ca 2+ accumulation and extensive neuronal injury in response to high concentrations of glutamate. These findings may be relevant to the observations of pre‐conditioning in the brain and heart.