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伏隔核中的二硝基喹喔啉抑制可卡因诱导的条件性位置偏爱。

DNQX in the nucleus accumbens inhibits cocaine-induced conditioned place preference.

作者信息

Kaddis F G, Uretsky N J, Wallace L J

机构信息

Division of Pharmacology, College of Pharmacy, Ohio State University, Columbus 43210-1291, USA.

出版信息

Brain Res. 1995 Oct 30;697(1-2):76-82. doi: 10.1016/0006-8993(95)00786-p.

Abstract

Several lines of evidence suggest that activation of both AMPA/kainate receptors and dopaminergic receptors in the nucleus accumbens may be required for psychostimulant drug induced reward. However, it has been reported that dopaminergic antagonists fail to block acquisition of conditioned place preference to cocaine. The goal of these experiments was to determine whether AMPA receptor antagonist injected into the nucleus accumbens could block conditioned place preference elicited by cocaine under conditions where dopaminergic antagonists do not inhibit acquisition of place preference. DNQX (1 microgram/0.5 microliter), injected into the nucleus accumbens just before systemic injections of cocaine (20 mg/kg i.p.) during the training sessions, attenuated the acquisition of place preference. This suggests that AMPA receptors are involved in acquisition of place preference to cocaine. By contrast, fluphenazine (2.5 micrograms/0.5 microliter), injected into the nucleus accumbens during training, did not alter cocaine-induced place preference. Analysis of locomotor activity showed that the ability of flyphenazine to inhibit cocaine-induced hyperactivity progressively decreased with each training session. These observations suggest that the failure of dopaminergic antagonists to block cocaine-induced place preference may be related to adaptations occurring following repeated exposure to these drugs. Both DNQX and fluphenazine blocked the expression of conditioned place preference in rats that had been previously trained with cocaine alone. This result suggests that both AMPA and dopaminergic receptors are involved in the expression of a conditioned place preference to cocaine.

摘要

多条证据表明,伏隔核中AMPA/海人藻酸受体和多巴胺能受体的激活可能是精神兴奋药物诱导奖赏所必需的。然而,有报道称多巴胺能拮抗剂无法阻断对可卡因的条件性位置偏爱习得。这些实验的目的是确定在多巴胺能拮抗剂不抑制位置偏爱习得的条件下,注入伏隔核的AMPA受体拮抗剂是否能阻断可卡因诱发的条件性位置偏爱。在训练期间,在全身注射可卡因(20mg/kg腹腔注射)之前,将DNQX(1微克/0.5微升)注入伏隔核,减弱了位置偏爱的习得。这表明AMPA受体参与了对可卡因的位置偏爱习得。相比之下,在训练期间将氟奋乃静(2.5微克/0.5微升)注入伏隔核,并未改变可卡因诱发的位置偏爱。对运动活性的分析表明,氟奋乃静抑制可卡因诱发的多动的能力在每次训练中逐渐下降。这些观察结果表明,多巴胺能拮抗剂无法阻断可卡因诱发的位置偏爱可能与反复接触这些药物后发生的适应性变化有关。DNQX和氟奋乃静都阻断了先前仅用可卡因训练的大鼠的条件性位置偏爱表达。这一结果表明,AMPA受体和多巴胺能受体都参与了对可卡因的条件性位置偏爱的表达。

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