Yount S E, Kraft M E, Pierce R C, Langley P E, Rebec G V
Department of Psychology, Indiana University, Bloomington 47405.
Life Sci. 1991;49(17):1237-44. doi: 10.1016/0024-3205(91)90136-y.
The ability of amphetamine to alter the extracellular level of ascorbate, an apparent modulator of neostriatal function, was assessed voltammetrically in the neostriatum and nucleus accumbens of awake, behaving rats. Whereas acute administration (1.0 and 5.0 mg/kg d-amphetamine) produced a dose-dependent rise in neostriatal ascorbate, there was no change in the nucleus accumbens. Vehicle injections had no significant effect on ascorbate levels in either location. Administration of 5.0 mg/kg d-amphetamine for one week enhanced neostriatal ascorbate release even further, but this effect returned to acute levels when treatment continued for a second week. Multiple amphetamine injections for up to two weeks failed to alter extracellular ascorbate in the nucleus accumbens. The results of these experiments confirm a site-specific action of amphetamine on ascorbate release and suggest complex changes in the extracellular level of this substance in the neostriatum with long-term treatment.
在清醒、活动的大鼠的新纹状体和伏隔核中,采用伏安法评估了苯丙胺改变细胞外抗坏血酸水平的能力,抗坏血酸是新纹状体功能的一种明显调节剂。急性给药(1.0和5.0mg/kg右旋苯丙胺)会使新纹状体中的抗坏血酸呈剂量依赖性升高,而伏隔核中则无变化。注射溶剂对这两个部位的抗坏血酸水平均无显著影响。连续一周给予5.0mg/kg右旋苯丙胺会进一步增强新纹状体中抗坏血酸的释放,但当治疗持续到第二周时,这种作用恢复到急性给药水平。连续两周多次注射苯丙胺未能改变伏隔核中的细胞外抗坏血酸水平。这些实验结果证实了苯丙胺对抗坏血酸释放具有位点特异性作用,并表明长期治疗会使新纹状体中该物质的细胞外水平发生复杂变化。