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亚慢性甲基苯丙胺治疗可增强甲基苯丙胺或可卡因在体内诱导的多巴胺外流。

Subchronic methamphetamine treatment enhances methamphetamine- or cocaine-induced dopamine efflux in vivo.

作者信息

Kazahaya Y, Akimoto K, Otsuki S

机构信息

Department of Neuropsychiatry, Okayama University Medical School, Japan.

出版信息

Biol Psychiatry. 1989 Apr 1;25(7):903-12. doi: 10.1016/0006-3223(89)90270-9.

Abstract

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.

摘要

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。

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