Collingridge G L, Kehl S J, McLennan H
Can J Physiol Pharmacol. 1984 Apr;62(4):424-9. doi: 10.1139/y84-067.
We have confirmed that gamma-D-glutamylglycine and the L-isomer of 2-amino-4-phosphonobutyric acid, and have shown also that L-2-amino-5-phosphonovaleric (L-APV) acid, are antagonists of synaptic excitations of dentate granule cells induced from both lateral and medial perforant paths. The N-methyl-D-aspartic acid (NMDA) antagonist D-APV is without effect. The synaptic antagonists reduce the presynaptic fibre volley particularly in the lateral path, suggesting that a reduced transmitter output contributes to their action. NMDA receptors exist upon the granule cells, but they are not involved with these synaptic process.
我们已证实γ-D-谷氨酰甘氨酸和2-氨基-4-膦酰丁酸的L-异构体,并且还表明L-2-氨基-5-膦酰戊酸(L-APV)是由外侧和内侧穿通通路诱导的齿状颗粒细胞突触兴奋的拮抗剂。N-甲基-D-天冬氨酸(NMDA)拮抗剂D-APV没有作用。这些突触拮抗剂尤其降低了外侧通路中的突触前纤维峰电位,这表明递质输出减少有助于它们发挥作用。NMDA受体存在于颗粒细胞上,但它们不参与这些突触过程。