Castle F, Evans R H, Kirkpatrick J N
Comp Biochem Physiol C Comp Pharmacol Toxicol. 1984;77(2):399-402. doi: 10.1016/0742-8413(84)90034-3.
The ED50 for loss of righting behaviour of cockroaches induced by kainate (43 mumol/kg body weight) indicated the toxicity of kainate to be much greater than would have been predicted from the excitatory action of this amino acid at insect skeletal muscle fibres. N-Methyl-D-aspartate had little effect on righting behaviour (ED50 greater than 3500 mumol/g body weight). Electrical recordings from the locust ventral nerve cord showed kainate (0.1-2 mM) to have a depolarizing action on neurons within the metathoracic ganglion. The depolarizing action of kainate was partially resistant to tetrodotoxin. The kainate-induced abolition of rostrally evoked potentials recorded in the abdominal connectives from the metathoracic ganglion suggests that the giant fibres are sensitive to kainate. Domoic acid was 46 times more potent than kainate. The lack of effect of N-methyl-D-aspartate (2 mM), dihydrokainate (2 mM), quisqualate (2 mM) and L-glutamate (20 mM) on nerve cords in the present experiments suggests that the kainate receptors in this preparation show a chemical selectivity comparable to that observed at vertebrate central neurones.
红藻氨酸(43微摩尔/千克体重)致使蟑螂翻正行为丧失的半数有效剂量(ED50)表明,红藻氨酸的毒性远大于根据该氨基酸对昆虫骨骼肌纤维的兴奋作用所预测的毒性。N-甲基-D-天冬氨酸对翻正行为几乎没有影响(ED50大于3500微摩尔/克体重)。对蝗虫腹神经索的电记录显示,红藻氨酸(0.1 - 2毫摩尔)对后胸神经节内的神经元有去极化作用。红藻氨酸的去极化作用对河豚毒素有部分抗性。红藻氨酸导致后胸神经节腹部神经索中记录的向前诱发电位消失,这表明巨纤维对红藻氨酸敏感。软骨藻酸的效力比红藻氨酸强46倍。在本实验中,N-甲基-D-天冬氨酸(2毫摩尔)、二氢红藻氨酸(2毫摩尔)、喹啉酸(2毫摩尔)和L-谷氨酸(20毫摩尔)对神经索均无影响,这表明该制剂中的红藻氨酸受体表现出与在脊椎动物中枢神经元中观察到的化学选择性相当的化学选择性。