Agmatine induces glutamate release and cell death in cultured rat cerebellar granule neurons

Abstract

We investigated the effect of agmatine on cell viability of rat cerebellar granule neurons in a high-K + (27.5 mM) medium. Exposure of cultured rat cerebellar granule neurons to agmatine (200–800 μM) resulted in a significant decrease in cell viability. Agmatine-induced neuronal death began to occur 6–12 h after addition, and gradually progressed. The agmatine neurotoxicity was attenuated by N-methyl- d-aspartate (NMDA) receptor antagonists and by enzymatic degradation of l-glutamate with glutamic pyruvic transaminase. Furthermore, a significant increase in extracellular l-glutamate concentration was detected before cell death occurred. In addition, agmatine-induced glutamate release and cell death were both blocked by pretreatment with botulinum toxin C, which is known to specifically inhibit the exocytosis. The agmatine neurotoxicity was not observed when extracellular K + concentration was lower (10 mM). These results suggest that agmatine induces glutamate release through the exocytosis and thereby causes NMDA receptor-mediated neuronal death in conditions in which extracellular K + concentrations are elevated.