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急性和反复接触甲苯后小鼠纹状体多巴胺动力学

Striatal dopamine dynamics in mice following acute and repeated toluene exposure.

作者信息

Apawu Aaron K, Mathews Tiffany A, Bowen Scott E

机构信息

Department of Chemistry, Wayne State University, 5101 Cass Ave, Detroit, MI, 48202, USA.

出版信息

Psychopharmacology (Berl). 2015 Jan;232(1):173-84. doi: 10.1007/s00213-014-3651-x. Epub 2014 Jul 5.

Abstract

RATIONALE

The abused inhalant toluene has potent behavioral effects, but only recently has progress been made in understanding the neurochemical actions that mediate the action of toluene in the brain. Available evidence suggests that toluene inhalation alters dopamine (DA) neurotransmission, but toluene's mechanism of action is unknown.

OBJECTIVE

The present study evaluated the effect of acute and repeated toluene inhalation (0, 2,000, or 4,000 ppm) on locomotor activity as well as striatal DA release and uptake using slice fast-scan cyclic voltammetry.

RESULTS

Acutely, 2,000 and 4,000 ppm toluene increased locomotor activity, while neurochemically only 4,000 ppm toluene potentiated electrically evoked DA release across the caudate-putamen and the nucleus accumbens. Repeated administration of toluene resulted in sensitization to toluene's locomotor activity effects. Brain slices obtained from mice repeatedly exposed to toluene demonstrated no difference in stimulated DA release in the caudate-putamen as compared to control animals. Repeated exposure to 2,000 and 4,000 ppm toluene caused a concentration-dependent decrease of 25-50 % in evoked DA release in the nucleus accumbens core and shell relative to air-exposed mice.

CONCLUSIONS

These voltammetric neurochemical findings following repeated toluene exposure suggest that there may be a compensatory downregulation of the DA system. Acute or repeated toluene exposure had no effect on the DA uptake kinetics. Taken together, these results demonstrate that acute toluene inhalation potentiates DA release, while repeated toluene exposure attenuates DA release in the nucleus accumbens only.

摘要

原理

滥用的吸入剂甲苯具有显著的行为效应,但直到最近,在理解介导甲苯在大脑中作用的神经化学作用方面才取得进展。现有证据表明,吸入甲苯会改变多巴胺(DA)神经传递,但甲苯的作用机制尚不清楚。

目的

本研究使用切片快速扫描循环伏安法评估急性和反复吸入甲苯(0、2000或4000 ppm)对运动活动以及纹状体DA释放和摄取的影响。

结果

急性吸入时,2000 ppm和4000 ppm的甲苯会增加运动活动,而在神经化学方面,只有4000 ppm的甲苯会增强整个尾状核-壳核和伏隔核的电诱发DA释放。反复给予甲苯会导致对甲苯运动活动效应的敏感化。与对照动物相比,从反复接触甲苯的小鼠获得的脑切片在尾状核-壳核中刺激的DA释放方面没有差异。相对于暴露于空气的小鼠,反复暴露于2000 ppm和4000 ppm的甲苯会导致伏隔核核心和壳中的诱发DA释放浓度依赖性降低25-50%。

结论

反复接触甲苯后的这些伏安神经化学研究结果表明,DA系统可能存在代偿性下调。急性或反复接触甲苯对DA摄取动力学没有影响。综上所述,这些结果表明,急性吸入甲苯会增强DA释放,而反复接触甲苯只会减弱伏隔核中的DA释放。

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