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某些抗精神病药物和右旋苯丙胺对小鼠纹状体中2-苯乙胺的影响。

The effects of some neuroleptics and d-amphetamine on striatal 2-phenylethylamine in the mouse.

作者信息

Juorio A V, Greenshaw A J, Zhu M Y, Paterson I A

机构信息

Department of Psychiatry, University of Saskatchewan, Saskatoon, Canada.

出版信息

Gen Pharmacol. 1991;22(2):407-13. doi: 10.1016/0306-3623(91)90473-j.

Abstract
  1. Mouse striatal 2-phenylethylamine was not changed at 2 hr following the administration of chlorpromazine, fluphenazine or spiperone. 2. In contrast, when the mice were first given pargyline (2 mg kg-1), treated with chlorpromazine, fluphenazine or spiperone 2 hr later and killed at 4 hr, a significant increase (to 130-170%) in the accumulation of 2-phenylethylamine was observed with respect to the pargyline controls. 3. The effect of chlorpromazine was consistently observed after pretreatment with either deprenyl (2 mg kg -1) or high doses (200 mg kg-1) of pargyline that produced different degrees of MAO inhibition. 4. Following pretreatment with pargyline (2 mg kg-1), d-amphetamine (5 mg kg-1) produced a significant reduction in striatal 2-phenylethylamine concentrations (to 39% of pargyline-treated controls). 5. The findings show that inhibition of dopamine transmission by neuroleptics increases the rate of 2-phenylethylamine accumulation. 6. Conversely, a stimulation of dopamine transmission by d-amphetamine results in a reduction in the rate of accumulation of 2-phenylethylamine and supports the concept of 2-phenylethylamine may be a neuromodulator of dopamine transmission.
摘要
  1. 给予氯丙嗪、氟奋乃静或螺哌隆后2小时,小鼠纹状体中的2-苯乙胺含量未发生变化。2. 相反,当小鼠先给予帕吉林(2毫克/千克),2小时后再用氯丙嗪、氟奋乃静或螺哌隆处理,并在4小时后处死时,相对于帕吉林对照组,观察到2-苯乙胺的积累显著增加(达到130%-170%)。3. 在用司来吉兰(2毫克/千克)或高剂量(200毫克/千克)的帕吉林进行预处理后,均持续观察到氯丙嗪的这种作用,这两种预处理产生了不同程度的单胺氧化酶抑制。4. 在用帕吉林(2毫克/千克)预处理后,右旋苯丙胺(5毫克/千克)使纹状体中2-苯乙胺浓度显著降低(降至帕吉林处理对照组的39%)。5. 这些发现表明,抗精神病药物对多巴胺传递的抑制会增加2-苯乙胺的积累速率。6. 相反,右旋苯丙胺对多巴胺传递的刺激导致2-苯乙胺积累速率降低,并支持2-苯乙胺可能是多巴胺传递的神经调节剂这一概念。

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