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Brain mitochondrial defects amplify intracellular [Ca 2+ ] rise and neurodegeneration but not Ca 2+ entry during NMDA receptor activation
Author(s) -
Jacquard Carine,
Trioulier Yael,
Cosker François,
Escartin Carole,
Bizat Nicolas,
Hantraye Philippe,
Manuel Cancela José,
Bonvento Gilles,
Brouillet Emmanuel
Publication year - 2006
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.05-5085fje
Subject(s) - excitotoxicity , nmda receptor , glutamate receptor , striatum , neurodegeneration , chemistry , calpain , neuroscience , long term potentiation , neuroprotection , kainic acid , agonist , microbiology and biotechnology , pharmacology , biology , receptor , biochemistry , medicine , disease , dopamine , enzyme
According to the "indirect" excitotoxicity hypothesis, mitochondrial defects increase Ca2+ entry into neurons by rendering NMDA-R hypersensitive to glutamate. We tested this hypothesis by investigating in the rat striatum and cultured striatal cells how partial mitochondrial complex II inhibition produced by 3-nitropropionic acid (3NP) modifies the toxicity of the NMDA-R agonist quinolinate (QA). We showed that nontoxic 3NP treatment, leading to partial inhibition of complex II activity, greatly exacerbated striatal degeneration produced by slightly toxic QA treatment through an "all-or-nothing" process. The potentiation of QA-induced cell death by 3NP was associated with increased calpain activity and massive calpain-mediated cleavage of several postsynaptic proteins, suggesting major neuronal Ca2+ deregulation in the striatum. However, Ca2+ anomalies probably do not result from NMDA-R hypersensitivity. Indeed, brain imaging experiments using [(18)F]fluorodeoxyglucose indirectly showed that 3NP did not increase QA-induced ionic perturbations at the striatal glutamatergic synapses in vivo. Consistent with this, the exacerbation of QA toxicity by 3NP was not related to an increase in the QA-induced entry of 45Ca2+ into striatal neurons. The present results demonstrate that the potentiation of NMDA-R-mediated excitotoxicity by mitochondrial defects involves primarily intracellular Ca2+ deregulation, in the absence of NMDA-R hypersensitivity.