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慢性应激会增强甲基苯丙胺的长期和急性效应。

Chronic stress augments the long-term and acute effects of methamphetamine.

作者信息

Matuszewich L, Yamamoto B K

机构信息

Department of Psychiatry, Case Western Reserve University, 11100 Euclid Avenue, Cleveland, OH 44106, USA.

出版信息

Neuroscience. 2004;124(3):637-46. doi: 10.1016/j.neuroscience.2003.12.007.

Abstract

There is growing evidence that exposure to stress alters the acute effects of abused drugs on the CNS. However, it is not known whether stress augments the longer-term neurotoxic effects of psychostimulant drugs, such as methamphetamine. Methamphetamine at high doses decreases forebrain dopamine concentrations. The current study tested the hypothesis that 10 days of unpredictable stress augmented striatal dopamine depletions 7 days following four injections of either 7.5 or 10 mg/kg methamphetamine (1 injection every 2 h). Furthermore, to assess the effects of chronic stress on immediate responses to methamphetamine, extracellular striatal dopamine and methamphetamine concentrations, and rectal temperature were monitored during the methamphetamine injection regimen. Seven days following either a 7.5 mg/kg or 10 mg/kg methamphetamine injection regimen, male rats exposed to unpredictable stress showed greater depletions in striatal dopamine tissue content compared with non-stressed controls injected with methamphetamine. Stressed rats had increased hyperthermic responses and dopamine efflux in the striatum during the methamphetamine injections when compared with non-stressed control rats. Moreover, stressed rats had an increased mortality rate (33%) compared with non-stressed controls (16.7%) following four injections of 10 mg/kg methamphetamine. The enhanced acute and longer-term effects of methamphetamine in stressed rats was not due to a greater concentrations of methamphetamine in the striatum, as extracellular levels of methamphetamine during the injection regimen did not differ between the two groups. In summary, exposure to 10 days of chronic unpredictable stress augments longer-term depletions of dopamine in the striatum, as well as acute methamphetamine-induced hyperthermia and extracellular dopamine levels. These findings suggest that chronic stress increases the responsiveness of the brain to the acute pharmacological effects of methamphetamine and enhances the vulnerability of the brain to the neurotoxic effects of psychostimulants.

摘要

越来越多的证据表明,暴露于应激会改变滥用药物对中枢神经系统的急性作用。然而,尚不清楚应激是否会增强精神刺激药物(如甲基苯丙胺)的长期神经毒性作用。高剂量的甲基苯丙胺会降低前脑多巴胺浓度。本研究检验了以下假设:在注射4次7.5或10mg/kg甲基苯丙胺(每2小时注射1次)后7天,10天的不可预测应激会加剧纹状体多巴胺耗竭。此外,为了评估慢性应激对甲基苯丙胺即时反应的影响,在甲基苯丙胺注射期间监测细胞外纹状体多巴胺和甲基苯丙胺浓度以及直肠温度。在接受7.5mg/kg或10mg/kg甲基苯丙胺注射方案后7天,暴露于不可预测应激的雄性大鼠与注射甲基苯丙胺的非应激对照相比,纹状体多巴胺组织含量的耗竭更大。与非应激对照大鼠相比,应激大鼠在注射甲基苯丙胺期间纹状体中的体温过高反应和多巴胺外流增加。此外,在注射4次10mg/kg甲基苯丙胺后,应激大鼠的死亡率(33%)高于非应激对照(16.7%)。应激大鼠中甲基苯丙胺增强的急性和长期作用并非由于纹状体中甲基苯丙胺浓度更高,因为注射期间两组间甲基苯丙胺的细胞外水平并无差异。总之,暴露于10天的慢性不可预测应激会加剧纹状体中多巴胺的长期耗竭,以及急性甲基苯丙胺诱导的体温过高和细胞外多巴胺水平。这些发现表明,慢性应激会增加大脑对甲基苯丙胺急性药理作用的反应性,并增强大脑对精神刺激药物神经毒性作用的易感性。

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