Quinolinic acid protects rat cerebellar granule cells from glutamate-induced apoptosis

Abstract

The effects of quinolinic acid (QUIN) on glutamate-induced excitotoxicity were examined in primary cultures of rat cerebellar granule neurons. Exposing these neurons to QUIN (≤2.5 mM) in the presence of glucose and Mg 2+ had no effect on their viability. Although pretreating neurons with QUIN (10 μM) for 6 h did not reduce necrotic death induced by glutamate exposure in the absence of glucose and Mg 2+, QUIN pretreatment significantly suppressed glutamate-induced apoptosis by 68% (as indicated by DNA fragmentation) in cultures containing glucose and Mg 2+. Furthermore, the N-methyl- d-aspartate (NMDA) receptor antagonist AP-5 reversed QUIN-induced neuroprotection, while the non-NMDA antagonist CNQX had no effect. This study demonstrates that pathophysiologically relevant concentrations of QUIN can protect neurons from apoptosis mediated via the NMDA receptor.