ffrench-Mullen J M, Hori N, Carpenter D O
J Neurophysiol. 1986 Jun;55(6):1283-94. doi: 10.1152/jn.1986.55.6.1283.
The actions of a variety of agonists and antagonists of the excitatory amino acids on rat pyriform cortex pyramidal neurons were studied in a submerged, perfused brain slice. The order of potency for the agonists, applied by ionophoresis, was kainate greater than quisqualate greater than N-methyl-D-aspartate greater than aspartate = glutamate. The endogenous monosynaptic excitation of pyramidal neurons upon stimulation of the lateral olfactory tract was blocked post-synaptically by DL-2-amino-4-phosphonobutyric acid, although this drug did not consistently block any of the exogenous responses. The synaptic excitation was not blocked, however, by antagonists presumed specific for the quisqualate (glutamate diethyl ester), kainate, (gamma-D-glutamylglycine), or N-methyl-D-aspartate (DL-2-amino-5-phosphonovaleric acid, DL-2-amino-7-phosphonohetaonic acid) receptors. Several antagonists blocked N-methyl-D-aspartate responses at lower concentrations than those to aspartate, and other antagonists distinguished between kainate and quisqualate responses. These results suggest that 1) pyriform neurons have a variety of receptors that have properties somewhat different from those found in other preparations and 2) the endogenous transmitter activates a receptor distinct from those activated by kainate, quisqualate, and N-methyl-D-aspartate.
在浸没式灌注脑片中研究了多种兴奋性氨基酸激动剂和拮抗剂对大鼠梨状皮质锥体神经元的作用。通过离子电泳施加的激动剂效力顺序为:海人酸大于喹啉酸大于N-甲基-D-天冬氨酸大于天冬氨酸=谷氨酸。刺激外侧嗅束时,锥体神经元的内源性单突触兴奋在突触后被DL-2-氨基-4-膦酸丁酸阻断,尽管该药物并不能始终阻断任何外源性反应。然而,推测对喹啉酸(谷氨酸二乙酯)、海人酸(γ-D-谷氨酰甘氨酸)或N-甲基-D-天冬氨酸(DL-2-氨基-5-膦酸戊酸、DL-2-氨基-7-膦酸庚酸)受体具有特异性的拮抗剂并未阻断突触兴奋。几种拮抗剂在比阻断天冬氨酸反应更低的浓度下阻断N-甲基-D-天冬氨酸反应,其他拮抗剂则区分了海人酸和喹啉酸反应。这些结果表明:1)梨状神经元具有多种受体,其特性与其他制剂中发现的受体有所不同;2)内源性递质激活的受体与海人酸、喹啉酸和N-甲基-D-天冬氨酸激活的受体不同。