Siarey R J, Long S K, Evans R H
DUPHAR B.V., Weesp, The Netherlands.
Eur J Pharmacol. 1991 Mar 26;195(2):241-4. doi: 10.1016/0014-2999(91)90541-w.
6-Cyano-7-nitroquinoxaline-2,3-dione (CNQX) (10 microM) depressed dorsal root-evoked ventral and dorsal root potentials of the in vitro immature rat spinal cord to 26.3 +/- 5.2 S.E.M. and 40.8 +/- 2.7% of control values respectively. These depressant effects of CNQX were partially reversed by D-serine (EC50 values 39.7 microM +/- 8.7 S.E.M. N = 6 and 34.9 +/- 12.5 microM, N = 5 for ventral root potential and dorsal root potential respectively). Under our experimental conditions, which included the presence of Mg2+ (0.75 mM) in the bathing medium, no measurable potentiation of these synaptic reflexes by D-serine was recorded in the absence of CNQX. These data indicate that CNQX, in addition to its depressant effect at non-NMDA receptors, depresses an NMDA receptor-mediated component of segmental transmission through its action at the glycine site of the NMDA receptor complex.
6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)(10微摩尔)分别将体外培养的未成熟大鼠脊髓背根诱发的腹根和背根电位降低至对照值的26.3±5.2%标准误和40.8±2.7%。D-丝氨酸可部分逆转CNQX的这些抑制作用(腹根电位和背根电位的EC50值分别为39.7微摩尔±8.7标准误,N = 6和34.9±12.5微摩尔,N = 5)。在我们的实验条件下,包括在浴液中存在Mg2+(0.75毫摩尔),在不存在CNQX的情况下,未记录到D-丝氨酸对这些突触反射的可测量增强作用。这些数据表明,CNQX除了在非NMDA受体处具有抑制作用外,还通过其在NMDA受体复合物甘氨酸位点的作用,抑制节段性传递中NMDA受体介导的成分。