Dommett E J, Simpson J, Clark D, Overton P G
Department of Psychology, University of Sheffield, Western Bank, Sheffield, UK.
J Neural Transm (Vienna). 2007 Feb;114(2):161-72. doi: 10.1007/s00702-006-0534-2. Epub 2006 Aug 8.
The induction of sensitisation to the behavioural effects of d-amphetamine - a model of drug addiction - involves the potentiation of exctiatory amino acid (EAA)-ergic synapses on dopaminergic neurons in the ventral tegmental area (VTA). Such potentiation has been reported as early as 2 hr post-injection, however earlier time points have not been assessed. Consequently, we examined the effects of systemic d-amphetamine on an EAA-mediated component of the VTA local field potential response to stimulation of the medial prefrontal cortex, an EAAergic afferent critical for sensitisation, over the immediate 2 hr post-injection period. D-amphetamine and saline both depressed the amplitude of this component to a similar extent throughout the recording session. It is concluded that overt aspects of EAA-mediated potentiation appear to be delayed with respect to drug administration, which may have implications for sensitisation's putative role in linking drug-related environmental stimuli and the central effects of the drug.
对右旋苯丙胺行为效应(一种药物成瘾模型)致敏作用的诱导涉及腹侧被盖区(VTA)中多巴胺能神经元上兴奋性氨基酸(EAA)能突触的增强。早在注射后2小时就已报道这种增强作用,然而更早的时间点尚未评估。因此,我们在注射后紧接着的2小时内,研究了全身性右旋苯丙胺对VTA局部场电位反应中EAA介导成分的影响,该反应是对内侧前额叶皮质刺激的反应,内侧前额叶皮质是致敏作用所必需的EAA能传入神经。在整个记录过程中,右旋苯丙胺和生理盐水均使该成分的幅度降低到相似程度。得出的结论是,EAA介导的增强作用的明显方面相对于药物给药似乎有所延迟,这可能对致敏作用在将与药物相关的环境刺激和药物的中枢效应联系起来的假定作用产生影响。