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对阿扑吗啡的致敏作用,地佐环平对NMDA受体的阻断效应。

Sensitization to apomorphine, effects of dizocilpine NMDA receptor blockades.

作者信息

Acerbo Martin J, Lee Jennifer M, Delius Juan D

机构信息

Allgemeine Psychologie, Universität Konstanz, 78457 Konstanz, Germany.

出版信息

Behav Brain Res. 2004 May 5;151(1-2):201-8. doi: 10.1016/j.bbr.2003.08.021.

DOI:10.1016/j.bbr.2003.08.021
PMID:15084436
Abstract

The dopamine agonist apomorphine (apo) elicits bouts of stereotyped pecking in pigeons, a response which increases with successive apo injections. This sensitization is strongly context-specific and has been suggested to arise through a Pavlovian conditioning to both external and internal cues. We hypothetized that this learning involves dopamino-glutamatergic interactions and investigated the issue by inducing NMDA glutamate receptor blockades with the antagonist dizocilpine (diz). A first experiment examined the effects that four different doses (ranging between 0.05 and 0.12 mg/kg) of diz co-administered with a standard dose of 0.5 mg/kg of apo had on the development of the incremented response and on the later expression of the conditioned pecking response. Both responses were impaired by doses of around 0.10 mg/kg diz. A second experiment assessed whether either a diz treatment or a diz plus apo co-treatment affected the development of a subsequent sensitization to apo. The first treatment had no effect on the latter sensitization. A part sensitization that arose with the second treatment did not transfer to the final sensitization. The last experiment examined whether the administration of diz had an immediate effect on the incremented responding to apo and on the conditioned response shown by already sensitized pigeons. No effect was apparent with the first treatment, but there was a marked response inhibition with the second treatment. It is concluded that NMDA glutamate receptors play an important role in apo-induced sensitization in pigeons which is compatible with the Pavlovian conditioning account of sensitization.

摘要

多巴胺激动剂阿扑吗啡(apo)能引发鸽子的刻板啄食行为,且随着apo的连续注射,这种反应会增强。这种敏化具有很强的情境特异性,有人认为它是通过对外部和内部线索的巴甫洛夫式条件作用产生的。我们推测这种学习涉及多巴胺能与谷氨酸能的相互作用,并通过用拮抗剂地佐环平(diz)诱导NMDA谷氨酸受体阻断来研究这个问题。第一个实验研究了与标准剂量0.5 mg/kg的apo共同给药的四种不同剂量(0.05至0.12 mg/kg)的diz对递增反应的发展以及对条件性啄食反应后期表达的影响。剂量约为0.10 mg/kg的diz会损害这两种反应。第二个实验评估了单独使用diz治疗或diz加apo联合治疗是否会影响随后对apo的敏化发展。第一种治疗对后一种敏化没有影响。第二种治疗产生的部分敏化并没有转化为最终的敏化。最后一个实验研究了给予diz是否对apo的递增反应以及已经致敏的鸽子所表现出的条件反应有即时影响。第一种治疗没有明显效果,但第二种治疗有明显的反应抑制作用。结论是,NMDA谷氨酸受体在鸽子的apo诱导的敏化中起重要作用,这与敏化的巴甫洛夫式条件作用解释是一致的。

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