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自由活动大鼠纹状体中电诱发细胞外多巴胺的实时测量。

Real-time measurement of electrically evoked extracellular dopamine in the striatum of freely moving rats.

作者信息

Garris P A, Christensen J R, Rebec G V, Wightman R M

机构信息

Department of Biological Sciences, Illinois State University, Normal, USA.

出版信息

J Neurochem. 1997 Jan;68(1):152-61. doi: 10.1046/j.1471-4159.1997.68010152.x.

Abstract

The real-time measurement of electrically evoked dopamine was established in brain extracellular fluid of freely moving rats. Dopamine was monitored by fast-scan cyclic voltammetry at carbon fiber microelectrodes lowered into the striatum by means of a detachable micromanipulator. A stimulating electrode, previously implanted in the substantia nigra, was used to evoke striatal dopamine efflux. Evoked extracellular dopamine was both current and frequency dependent. When low current intensities (+/-125 microA) and frequencies (10-20 Hz) were applied, detectable levels of dopamine were elicited without a perceptible behavioral response. Reproducible concentrations of extracellular dopamine could be evoked in the same rat for at least 2 months. These concentrations, moreover, were significantly higher in freely moving rats compared with rats anesthetized with Equithesin. Analysis of measured curves for dopamine uptake and release rates revealed that anesthesia inhibits release but does not affect uptake. It is concluded that (a) fast-scan cyclic voltammetry at carbon fiber microelectrodes is a viable technique for the measurement of electrically evoked dopamine in brain extracellular fluid of freely moving rats, (b) it is possible to determine in situ rate constants for dopamine release and uptake from these temporally and spatially resolved measurements of levels of dopamine, and (c) transient changes in extracellular dopamine levels elicited by electrical stimulation are affected by anesthesia.

摘要

在自由活动大鼠的脑海马沟液中建立了电诱发多巴胺的实时测量方法。通过可拆卸的微操纵器将碳纤维微电极插入纹状体,利用快速扫描循环伏安法监测多巴胺。先前植入黑质的刺激电极用于诱发纹状体多巴胺流出。诱发的细胞外多巴胺既与电流有关,也与频率有关。当施加低电流强度(±125微安)和频率(10 - 20赫兹)时,可检测到多巴胺水平,且无明显行为反应。在同一只大鼠中,可重复诱发细胞外多巴胺浓度至少2个月。此外,与用戊巴比妥钠和水合氯醛麻醉的大鼠相比,自由活动大鼠的这些浓度显著更高。对多巴胺摄取和释放速率的测量曲线分析表明,麻醉会抑制释放,但不影响摄取。得出以下结论:(a) 碳纤维微电极上的快速扫描循环伏安法是测量自由活动大鼠脑海马沟液中电诱发多巴胺的可行技术;(b) 根据这些多巴胺水平的时间和空间分辨测量结果,可以原位确定多巴胺释放和摄取的速率常数;(c) 电刺激引起的细胞外多巴胺水平的瞬时变化受麻醉影响。

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