Partial Involvement of Group I Metabotropic Glutamate Receptors in the Neurotoxicity of 3-N-Oxalyl-L-2,3-diaminopropanoic Acid(L-β-ODAP)(Pharmacology)

概要

論文の詳細を見る
Neurolathyrism is a human motoneuron disease caused by the overconsumption of grass pea (Lathyrus sativus) that contains a toxic non-protein amino acid, S-N-oxalyl-L-2,3-diaminopropanoic acid (L-β-ODAP). The preventive activities of various glutamatergic agents from acute neuronal death caused by L-β-ODAP were studied using rat primary cortical neuron/glia culture. Nearly 80% of the rat primary cortical neurons were killed by 300 μM L-β-ODAP within 24 h. Though antagonists acting on the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor prevented most of the toxicity, antagonists acting on group I metabotropic glutamatergic receptors (mGluRs), including (RS)-1-aminoindan-l,5-dicarboxylic acid (AIDA), (S)-α-methyl-4-carboxyphenylglycine (MCPG), and 2-methyl-6-(2-phenylethenyl)pyridine (SIB1893) partially and significantly prevented neuronal death due to L-β-ODAP. These antagonists, within limited concentrations, did not have any inhibitory effects on the currents through AMPA receptors expressed in Xenopm oocytes. L-β-ODAP itself did not induce the currents through group I mGluRs expressed in Xenopm oocytes. These results suggest that the neurotoxicity induced by L-β-ODAP is partially mediated by the activation of group I mGluRs by an indirect mechanisms.
公益社団法人日本薬学会の論文
2004-07-01