Luquin M R, Obeso J A, Laguna J, Guillén J, Martínez-Lage J M
Department of Neurology, Clínica Universitaria de Navarra, Medical School, Pamplona, Spain.
Eur J Pharmacol. 1993 Apr 28;235(2-3):297-300. doi: 10.1016/0014-2999(93)90149-c.
We studied the motor response induced by the administration of the AMPA receptor antagonist, NBQX (2,3-dihydroxy-6-nitro-7-sulfamoylbenzo[f]quinoxaline(1H,4H)dione sodium salt), in two parkinsonian monkeys and its interaction with the selective D-2 dopamine receptor agonist, (+)-PHNO [(+)-4-propyl-9-hydroxynaphthoxazine], and the partial dopamine D-1 receptor agonist, CY 208-243 [(-)-4,6,6a,7,8,12b-hexahydro-7-methyl-indolo[4,3a-b]phen anthyxidine]. NBQX treatment did not reverse the parkinsonism or change the responses previously induced by dopamine agonists. These results do not support an antiparkinsonian effect of the AMPA receptor antagonist, NBQX. In addition they indicate that there is no functional interaction between AMPA and dopamine receptors in monkeys with a substantia nigra lesion.
我们研究了在两只帕金森病猴中给予AMPA受体拮抗剂NBQX(2,3 - 二羟基 - 6 - 硝基 - 7 - 氨磺酰基苯并[f]喹喔啉(1H,4H)二酮钠盐)所诱导的运动反应,以及它与选择性D - 2多巴胺受体激动剂(+)-PHNO [(+)-4 - 丙基 - 9 - 羟基萘并恶嗪]和部分多巴胺D - 1受体激动剂CY 208 - 243 [( - )-4,6,6a,7,8,12b - 六氢 - 7 - 甲基 - 吲哚并[4,3a - b]菲啶]的相互作用。NBQX治疗并未逆转帕金森病状态,也未改变先前由多巴胺激动剂诱导的反应。这些结果不支持AMPA受体拮抗剂NBQX具有抗帕金森病作用。此外,它们表明在患有黑质损伤的猴子中,AMPA和多巴胺受体之间不存在功能相互作用。