Suppr超能文献

低剂量阿扑吗啡在无条件作用的情况下诱导情境特异性运动减少敏化:支持药物条件作用和敏化的一种新的状态依赖性检索假说。

Low dose apomorphine induces context-specific sensitization of hypolocomotion without conditioning: support for a new state dependent retrieval hypothesis of drug conditioning and sensitization.

作者信息

Braga Priscila Quintanilha, Dias Flávia Regina Cruz, Carey Robert J, Carrera Marinete Pinheiro

机构信息

Behavioral Pharmacology Group, Laboratory of Animal Health, State University of North Fluminense, Campos dos Goytacazes, RJ, Brazil.

出版信息

Pharmacol Biochem Behav. 2009 Aug;93(2):128-33. doi: 10.1016/j.pbb.2009.04.019. Epub 2009 May 3.

Abstract

High doses of apomorphine induce sensitization to locomotor stimulant effects whereas low doses induce locomotor inhibition. We examined whether repeated low dose apomorphine induced sensitization and conditioning to the locomotor inhibitory effect. Three doses of the D1/D2 agonist, apomorphine, were used in a Pavlovian conditioning protocol: 0.05 mg/kg (autoreceptor level), 0.5 and 2.0 mg/kg (post-synaptic level). Rats received 5 daily apomorphine treatments paired or unpaired to an open-field environment (conditioning phase) followed by a saline test (conditioning test) and an apomorphine challenge test (sensitization test). Locomotion was measured for 30 min. During the acquisition phase, the 0.05 mg/kg paired treatment decreased locomotion while the high dose paired treatments increased locomotion. The 0.05 mg/kg paired treatment did not induce conditioning but induced inhibitory locomotor sensitization. The post-synaptic paired treatments produced conditioned and sensitized locomotor stimulation. For the low dose results, we propose an expanded contextual stimulus, which includes interoceptive drug cues. In the sensitization test, the same interoceptive drug cues and test environment cues are present as those during acquisition. In the conditioning test, normative dopaminergic activity is present which generates internal cues that may or may not generalize to the drug-induced cues and, permit or prevent retrieval of conditioning.

摘要

高剂量阿扑吗啡可诱导对运动兴奋作用的敏化,而低剂量则诱导运动抑制。我们研究了重复低剂量阿扑吗啡是否会诱导对运动抑制作用的敏化和条件反射。在巴甫洛夫条件反射实验方案中使用了三种剂量的D1/D2激动剂阿扑吗啡:0.05毫克/千克(自身受体水平)、0.5毫克/千克和2.0毫克/千克(突触后水平)。大鼠每天接受5次阿扑吗啡处理,与旷场环境配对或不配对(条件反射阶段),随后进行生理盐水测试(条件反射测试)和阿扑吗啡激发测试(敏化测试)。测量30分钟内的运动情况。在习得阶段,0.05毫克/千克的配对处理降低了运动,而高剂量的配对处理增加了运动。0.05毫克/千克的配对处理未诱导条件反射,但诱导了抑制性运动敏化。突触后配对处理产生了条件性和敏化性运动刺激。对于低剂量结果,我们提出了一种扩展的情境刺激,其中包括内感受性药物线索。在敏化测试中,存在与习得期间相同的内感受性药物线索和测试环境线索。在条件反射测试中,存在正常的多巴胺能活动,其产生的内部线索可能会或可能不会推广到药物诱导的线索,并允许或阻止条件反射的恢复。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验