Piercey M F, Hoffmann W E, Kaczkofsky P
CNS Research, Upjohn Company, Kalamazoo, MI 49001.
Psychopharmacology (Berl). 1988;96(4):561-2. doi: 10.1007/BF02180042.
MK-801 is an indirect antagonist of the NMDA excitatory amino acid receptor which is being considered for possible clinical development for treatment of epilepsy and stroke. MK-801 was evaluated for its effects on regional brain energy metabolism by means of Sokoloff's 2-deoxyglucose (2-DG) autoradiography method. MK-801 produced dramatic alterations in regional energy metabolism, exciting Papez circuit and dopaminergic structures most intensely. The pattern of metabolic alterations was virtually indistinguishable from that previously described for the psychotomimetic drug of abuse, phencyclidine (PCP). It is concluded that MK-801 is at risk for possibly producing PCP-like psychotomimetic effects.
MK-801是N-甲基-D-天冬氨酸(NMDA)兴奋性氨基酸受体的间接拮抗剂,正被考虑用于癫痫和中风治疗的临床开发。通过索科洛夫的2-脱氧葡萄糖(2-DG)放射自显影法评估了MK-801对局部脑能量代谢的影响。MK-801引起了局部能量代谢的显著改变,对帕佩兹环路和多巴胺能结构的兴奋最为强烈。代谢改变的模式与先前描述的滥用拟精神病药物苯环利定(PCP)的模式几乎无法区分。得出的结论是,MK-801有可能产生类似PCP的拟精神病作用。