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Sensitization of amphetamine-induced stereotyped behaviors during the acute response.

机译:急性反应期间苯丙胺诱导的刻板行为的敏化。

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摘要

The quantitative and qualitative features of the behavioral response to amphetamine-like stimulants in rats can be dissociated from the dopamine response. This dissociation is particularly evident in the temporal profiles of the extracellular dopamine and stereotypy responses to higher doses of amphetamine. One possible mechanism contributing to this temporal dissociation is that during the acute response to amphetamine, dopamine receptor mechanisms are enhanced such that stereotyped behaviors can be supported by synaptic concentrations of dopamine which are not sufficient to initiate these behaviors. To further explore the dynamics of stimulant sensitivity during the acute response, we examined the behavioral and extracellular dopamine responses to a low, nonstereotypy-producing dose of amphetamine (0.5 mg/kg) at various times after an acute, priming injection of 4.0 mg/kg when stereotypies had subsided and extracellular dopamine was approaching predrug baseline levels. The low-dose challenge produced intense stereotypies although the regional dopamine responses were not significantly different from control animals. Blockade of the expression of stereotypies during the priming response by the D2 antagonist haloperidol or the D1 antagonist SCH 23390 prevented the expression of an enhanced stereotypy response to the challenge injection. Our results suggest that an exposure to amphetamine results in a rapid sensitization of the stereotypy response which does not involve changes in the extracellular dopamine response but requires activation of dopamine receptors. Such a mechanism may be significantly implicated during binge patterns of stimulant abuse and may also play a role in the sensitization associated with repeated amphetamine administration.
机译:在大鼠中对苯丙胺样兴奋剂的行为反应的定量和定性特征可以与多巴胺反应分离。这种解离在细胞外多巴胺的时间变化和对高剂量苯丙胺的定型反应中特别明显。导致这种暂时解离的一种可能的机制是,在对苯丙胺的急性反应期间,多巴胺受体机制得到增强,以致刻板行为可以由不足以引发这些行为的突触浓度的多巴胺来支持。为了进一步探讨急性反应过程中兴奋剂敏感性的变化,我们研究了急性和初次注射4.0 mg / ml后不同时间对低,非定型产生剂量的苯丙胺(0.5 mg / kg)的行为和细胞外多巴胺反应。当刻板印象消退并且细胞外多巴胺接近药物前基线水平时,kg。尽管区域多巴胺反应与对照动物无显着差异,但低剂量激发产生强烈的定型观念。 D2拮抗剂氟哌啶醇或D1拮抗剂SCH 23390在启动反应过程中对刻板印象的表达进行了阻止,从而阻止了对激发注射的刻板反应的增强表达。我们的结果表明,接触苯丙胺会导致刻板印象反应迅速敏化,这不涉及细胞外多巴胺反应的改变,但需要激活多巴胺受体。这种机制可能在兴奋剂滥用的暴涨模式中显着地牵涉,并且也可能在与重复安非他明给药有关的致敏作用中起作用。

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