Salt T E, Hill R G
Neuropharmacology. 1982 May;21(5):385-90. doi: 10.1016/0028-3908(82)90020-x.
The excitatory amino acid antagonist, D-alpha-aminoadipate, was found to be a potent antagonist of responses to N-methyl-D-aspartate and L-aspartate, but less potent against L-glutamate responses of neurones in the rat caudal trigeminal nucleus. The responses to quisqualate and kainate were relatively unaffected by D-alpha-aminoadipate, but were antagonized by the two antagonists cis-2,3-piperidine dicarboxylate and gamma-D-glutamylglycine. These two antagonists had effectively similar spectra of activity. It is concluded that there is a distinct N-methyl-D-aspartate receptor in the trigeminal nucleus caudalis, and that kainate and quisqualate may act on a different, but common, receptor. Exogenously applied L-glutamate appears to act at both of these receptors, but exogenously applied L-aspartate appears to act almost exclusively on a D-alpha-aminoadipate sensitive site that may be the N-methyl-D-aspartate receptor. The kainate/quisqualate receptor is thought to be involved in the synaptic excitation of neurones in the caudal trigeminal nucleus by non-noxious mechanical stimuli.
兴奋性氨基酸拮抗剂D-α-氨基己二酸被发现是对N-甲基-D-天冬氨酸和L-天冬氨酸反应的强效拮抗剂,但对大鼠尾侧三叉神经核中神经元的L-谷氨酸反应的效力较弱。对喹啉酸和海人藻酸的反应相对不受D-α-氨基己二酸的影响,但被两种拮抗剂顺式-2,3-哌啶二羧酸和γ-D-谷氨酰甘氨酸拮抗。这两种拮抗剂具有相似的有效活性谱。得出的结论是,在尾侧三叉神经核中存在一种独特的N-甲基-D-天冬氨酸受体,并且海人藻酸和喹啉酸可能作用于不同但共同的受体。外源性应用的L-谷氨酸似乎作用于这两种受体,但外源性应用的L-天冬氨酸似乎几乎只作用于一个对D-α-氨基己二酸敏感的位点,该位点可能是N-甲基-D-天冬氨酸受体。海人藻酸/喹啉酸受体被认为参与了无害机械刺激对尾侧三叉神经核中神经元的突触兴奋。