Kurumaji A, Aihara O, Yamada S, Toru M
Department of Neuropsychiatry, Tokyo Medical and Dental University School of Medicine, 1-5-45 Yushima, Bunkyo-ku, 113-8519, Tokyo, Japan.
Brain Res Dev Brain Res. 2000 Nov 30;124(1-2):125-7. doi: 10.1016/s0165-3806(00)00107-3.
We examined the effects of neonatal treatment with MK-801 on 1-(2, 5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI)-induced head shaking as well as [(3)H]ketanserin binding in adult rats. Neonatal rats were injected with MK-801 (0.25 mg/kg, s.c., twice daily) or with saline from postnatal days (PND) 7-18. At PND 60, a statistically significant increase in the frequency of head shaking induced by DOI (1.0 mg/kg, s.c.) was observed in the rats neonatally treated with MK-801, compared to saline-treated rats, without any change in the specific [(3)H]ketanserin binding in the frontal cortex. These results suggest that repeated NMDA receptor blockades during the critical period of brain development produce a long lasting hyper-responsiveness in the 5-HT(2A) receptor-mediated behavior, interfering with the development of neural circuits related to the behavior.
我们研究了新生大鼠用MK-801治疗对成年大鼠中1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷(DOI)诱导的头部抖动以及[(3)H]酮色林结合的影响。新生大鼠从出生后第7天至第18天每天皮下注射两次MK-801(0.25mg/kg)或生理盐水。在出生后第60天,与生理盐水处理的大鼠相比,用MK-801进行新生期处理的大鼠中,由DOI(1.0mg/kg,皮下注射)诱导的头部抖动频率有统计学意义的增加,而额叶皮质中特异性[(3)H]酮色林结合没有任何变化。这些结果表明,在脑发育的关键时期反复进行NMDA受体阻断会在5-HT(2A)受体介导的行为中产生持久的高反应性,干扰与该行为相关的神经回路的发育。