Corbett D
Division Basic Medical Sciences, Memorial University of Newfoundland, St. John's, Canada.
Behav Brain Res. 1989 Sep 1;34(3):239-46. doi: 10.1016/s0166-4328(89)80105-6.
Selective antagonists of the N-methyl-D-aspartate (NMDA) receptor such as MK-801 may have therapeutic potential in the treatment of ischemic brain injury. However, some drugs (e.g. ketamine and phencyclidine) with potent NMDA antagonist properties are also addictive. Intracranial self-stimulation (ICSS) is facilitated by drugs of abuse such as cocaine and amphetamine and thus is useful for screening compounds with potential abuse liability. Low doses of the NMDA antagonist, MK-801 were also found to facilitate ICSS, suggesting that this compound may possess abuse potential.
N-甲基-D-天冬氨酸(NMDA)受体的选择性拮抗剂,如MK-801,可能在治疗缺血性脑损伤方面具有治疗潜力。然而,一些具有强效NMDA拮抗剂特性的药物(如氯胺酮和苯环己哌啶)也会上瘾。滥用药物如可卡因和苯丙胺可促进颅内自我刺激(ICSS),因此可用于筛选具有潜在滥用可能性的化合物。低剂量的NMDA拮抗剂MK-801也被发现可促进ICSS,这表明该化合物可能具有滥用潜力。