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麻醉小鼠中莫达非尼活性缺乏突触前多巴胺能参与:体内伏安法研究

Lack of pre-synaptic dopaminergic involvement in modafinil activity in anaesthetized mice: in vivo voltammetry studies.

作者信息

De Séréville J E, Boer C, Rambert F A, Duteil J

机构信息

Centre de Recherches, Maisons-Alfort, France.

出版信息

Neuropharmacology. 1994 Jun;33(6):755-61. doi: 10.1016/0028-3908(94)90115-5.

Abstract

Modafinil was compared to the indirect dopaminergic drugs, dexamphetamine and methylphenidate, using in vivo differential normal pulse voltammetry with carbon fibre electrodes located in the caudate nucleus to study extracellular catechol level in anaesthetized mice. Modafinil (16-256 mg kg-1) failed to modify the catechol oxidation peak height (peak 2). Dexamphetamine at low doses (2 and 4 mg kg-1) decreased, while at a higher dose (8 mg kg-1) did not modify peak 2 height. A low dose of methylphenidate (16 mg kg-1) did not display any effect, while higher doses (32 and 64 mg kg-1) increased peak 2 height. Pargyline-induced monoamine oxidase inhibition elicited a rapid and dramatic decrease in peak 2 height (related to the decrease of catechol levels). In these conditions modafinil (64 and 256 mg kg-1) did not modify, while dexamphetamine (2, 4 and 8 mg kg-1) and methylphenidate (16, 32 and 64 mg kg-1) increased peak 2 height in relation to synaptic dopamine level increase. This study, in mice, demonstrated the lack of effects of modafinil on nigro-striatal function, at the pre-synaptic level, as opposed to dexamphetamine and methylphenidate.

摘要

使用位于尾状核的碳纤维电极进行体内差分正常脉冲伏安法,以研究麻醉小鼠的细胞外儿茶酚水平,将莫达非尼与间接多巴胺能药物右苯丙胺和哌甲酯进行比较。莫达非尼(16 - 256毫克/千克)未能改变儿茶酚氧化峰高(峰2)。低剂量(2和4毫克/千克)的右苯丙胺可降低峰2高度,而高剂量(8毫克/千克)则不改变峰2高度。低剂量的哌甲酯(16毫克/千克)未显示任何作用,而高剂量(32和64毫克/千克)可增加峰2高度。帕吉林诱导的单胺氧化酶抑制导致峰2高度迅速且显著降低(与儿茶酚水平降低有关)。在这些条件下,莫达非尼(64和256毫克/千克)未改变峰2高度,而右苯丙胺(2、4和8毫克/千克)和哌甲酯(16、32和64毫克/千克)则随着突触多巴胺水平的增加而增加峰2高度。在小鼠中的这项研究表明,与右苯丙胺和哌甲酯不同,莫达非尼在突触前水平对黑质 - 纹状体功能没有影响。

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