Kazahaya Y, Akimoto K, Otsuki S
Department of Neuropsychiatry, Okayama University Medical School, Japan.
Biol Psychiatry. 1989 Apr 1;25(7):903-12. doi: 10.1016/0006-3223(89)90270-9.
Intracerebral dialysis was used to study the mechanism underlying behavioral sensitization. Rats were divided into two groups: a control group that received intraperitoneal injections of saline and an experimental group that was given methamphetamine (MAP) (4 mg/kg) once a day for 14 days. Seven days after the last injection, dopamine (DA) and its metabolites were measured in striatal dialysates obtained from awake freely moving rats. A challenge injection of MAP (4 mg/kg) caused a marked increase in the extracellular concentrations of DA, and the extent of the increase was significantly greater in MAP-pretreated rats than in the saline-pretreated controls. A challenge injection of cocaine (20 mg/kg) also caused a significantly greater increase in extracellular DA levels in MAP-pretreated rats than in saline-pretreated rats. These results suggest that an enhancement in striatal DA efflux may play an important role in MAP-induced behavioral sensitization and cross-sensitization to cocaine.
采用脑内透析技术研究行为敏化的潜在机制。将大鼠分为两组:一组为对照组,腹腔注射生理盐水;另一组为实验组,每天给予甲基苯丙胺(MAP)(4毫克/千克),持续14天。末次注射7天后,在清醒自由活动大鼠的纹状体透析液中检测多巴胺(DA)及其代谢产物。给予MAP(4毫克/千克)激发注射后,细胞外DA浓度显著升高,且MAP预处理大鼠的升高幅度明显大于生理盐水预处理的对照组。给予可卡因(20毫克/千克)激发注射后,MAP预处理大鼠的细胞外DA水平升高幅度也显著大于生理盐水预处理大鼠。这些结果表明,纹状体DA外流增强可能在MAP诱导的行为敏化及对可卡因的交叉敏化中起重要作用。