Ujike H, Akiyama K, Nishikawa H, Onoue T, Otsuki S
Department of Neuropsychiatry, Okayama University Medical School, Japan.
Brain Res. 1991 Feb 1;540(1-2):159-63. doi: 10.1016/0006-8993(91)90503-n.
To examine the possible involvement of D1 dopamine receptors in behavioral sensitization induced by subchronic methamphetamine (MAP) administration, regional D1 receptors labeled with [3H]SCH 23390 were examined using binding assay and quantitative autoradiography. Rats received 4 mg/kg/day MAP (i.p.) for 14 days, and were decapitated after an abstinence period of 24 h, 7 days or 21 days. In MAP-treated rats, a significant decrease in Kd in the mesolimbic area was observed 24 h but not 7 days after the last injection. Neither Kd nor Bmax changed in the striatum or medial prefrontal cortex of MAP-treated rats after any period of abstinence. Autoradiography revealed a significant increase in specific [3H]SCH 22390 binding in the lateral part of the substantia nigra pars reticulata (SNr) of MAP-treated rats. Since this increase lasted up to 21 days after cessation of subchronic MAP administration, it is suggested that lasting increase in the nigral D1 receptors may be associated with the biological changes underlying MAP-induced behavioral sensitization.
为研究D1多巴胺受体是否可能参与由亚慢性给予甲基苯丙胺(MAP)诱导的行为敏化,采用结合测定和定量放射自显影法检测用[3H]SCH 23390标记的区域D1受体。大鼠连续14天腹腔注射4 mg/kg/天的MAP,在戒断24小时、7天或21天后断头。在MAP处理的大鼠中,末次注射后24小时观察到中脑边缘区域的解离常数(Kd)显著降低,但7天后未观察到。在任何戒断期后,MAP处理的大鼠纹状体或内侧前额叶皮质的Kd和最大结合容量(Bmax)均未改变。放射自显影显示,MAP处理的大鼠黑质网状部(SNr)外侧部分的特异性[3H]SCH 22390结合显著增加。由于这种增加在亚慢性MAP给药停止后持续长达21天,提示黑质D1受体的持续增加可能与MAP诱导的行为敏化的生物学变化有关。