Ferkany J W, Borosky S A, Clissold D B, Pontecorvo M J
Nova Pharmaceutical Corporation, Baltimore, MD 21224-2788.
Eur J Pharmacol. 1988 Jun 22;151(1):151-4. doi: 10.1016/0014-2999(88)90707-8.
Dextromethorphan, its metabolite dextrorphan, phencyclidine, ketamine, MK-801, 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid and DL-2-amino-7-phosphonoheptanoic acid were evaluated for potency to antagonize N-methyl-D-aspartate-induced convulsions following intraperitoneal administration using male CF-1 mice. Whereas reference anticonvulsants (e.g., phenytoin) were ineffective in this model, dextromethorphan and all competitive and noncompetitive N-methyl-D-aspartate antagonists blocked seizures. The results are consistent with the interpretation that dextromethorphan elicits some of its pharmacological responses via an interaction with receptors for excitatory amino acids.
使用雄性CF - 1小鼠,对右美沙芬及其代谢产物右啡烷、苯环利定、氯胺酮、MK - 801、3 -(2 - 羧基哌嗪 - 4 - 基)丙基 - 1 - 膦酸和DL - 2 - 氨基 - 7 - 膦酸庚酸进行腹腔注射后拮抗N - 甲基 - D - 天冬氨酸诱导惊厥的效力评估。虽然参考抗惊厥药(如苯妥英)在该模型中无效,但右美沙芬以及所有竞争性和非竞争性N - 甲基 - D - 天冬氨酸拮抗剂均可阻断癫痫发作。这些结果与以下解释一致:右美沙芬通过与兴奋性氨基酸受体相互作用引发其一些药理反应。