PENTAMIDINE, AN INHIBITOR OF SPINAL FLEXOR REFLEXES IN RATS, IS A POTENT N-METHYL-D-ASPARTATE (NMDA) ANTAGONIST IN-VIVO

被引:7
作者
BLOCK, F [1 ]
SCHMITT, T [1 ]
SCHWARZ, M [1 ]
机构
[1] RHEIN WESTFAL TH AACHEN,DEPT NEUROL,W-5100 AACHEN,GERMANY
关键词
PENTAMIDINE; N-METHYL-D-ASPARTATE; FLEXOR REFLEX; RAT;
D O I
10.1016/0304-3940(93)90709-T
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The present study examined whether the antimicrobial agent pentamidine exerts an antagonistic action at the N-methyl-D-aspartate (NMDA) receptor as tested on spinal reflexes in rats in vivo. After intrathecal injection both the specific NMDA antagonist (-)-2-amino-7-phosphonoheptanoate and pentamidine dose-dependently reduced the magnitude of the polysynaptic flexor reflex without affecting the monosynaptic H-reflex. In contrast, the non-NMDA antagonist 6,7-dinitroquinoxaline-2,3-dione depressed the H-reflex in a dose-dependent manner without affecting the flexor reflex. The depressant effect of pentamidine on the flexor reflex was prevented by coadministration with NMDA but not with the non-NMDA agonist alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid. These data suggest that pentamidine exerts an antagonistic action at the NMDA receptor in vivo.
引用
收藏
页码:208 / 211
页数:4
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