急性甲苯暴露时大鼠腹侧被盖多巴胺神经元活动的电生理分析。

A C Riegel, E D French
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引用次数: 49

摘要

吸入剂滥用是一种常见的、潜在致命的药物滥用形式。虽然一些普遍滥用的吸入剂中假定的精神药物成分似乎经常是有机溶剂甲苯,但其对构成奖赏通路的中脑神经元的影响尚未确定。因此,本研究旨在评估腹侧被盖多巴胺神经元在吸入甲苯时的反应。将氯胺酮麻醉的大鼠暴露在与吸入剂滥用者相似的急性(1-15.3分钟)浓度的甲苯蒸气(11,500 ppm)中,使用细胞外单单位记录进行电生理测定。通过气管呼吸管接触甲苯会引起多巴胺神经元两种截然不同的反应模式。一种模式包括初始刺激神经元放电(+221%+/-72%;8.5分钟)。另一种模式只包括抑制放电,而不管暴露的时间长短。此外,放电速率的变化与脉冲中动作电位数量的变化是平行的。在多巴胺记录时采集的血液样本显示,无论反应模式如何,甲苯浓度都相当(4-79微克/毫升,n=24)。这些结果表明,中边缘多巴胺神经传递可以通过类似于人类滥用者使用的暴露范式而改变,这些变化可能是吸入剂滥用的强化效应的组成部分。
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An electrophysiological analysis of rat ventral tegmental dopamine neuronal activity during acute toluene exposure.

Inhalant abuse is a common, potentially lethal, form of drug abuse. Although the putative psychotropic component of some popularly abused inhalants appears often to be the organic solvent toluene, its effects on midbrain neurones which comprise reward pathways have not been established. Therefore, the present study was designed to assess the response of ventral tegmental dopamine neurones during toluene inhalation. Electrophysiological determinations were made using extracellular single-unit recordings in ketamine anaesthetized rats that were exposed to acute (1-15.3 min.) concentrations of toluene vapor (11,500 ppm) similar to those consumed by inhalant abusers. Toluene exposure through a tracheal breathing tube elicited two distinctly different patterns of response in dopamine neurons. One pattern consisted of an initial stimulation of neuronal firing (+221%+/-72%; <8.5 min.) followed by an attenuation of the firing rate with continued exposure (+58.7%+/-6.3%; >8.5 min.). The other pattern consisted of only an inhibition of firing regardless of the length of exposure. Furthermore, the changes in firing rates were paralleled by changes in number of action potentials contained in bursts. Blood samples taken at the time of the dopamine recordings revealed comparable toluene concentrations (4-79 microg/ml, n=24) regardless of the patterns of response. These results suggest that mesolimbic dopamine neurotransmission can be changed by an exposure paradigm comparable to that used by human abusers, and that these changes may be integral to the reinforcing effects underlying inhalant abuse.

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