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前边缘皮层失活会损害情境诱导的乙醇寻求行为恢复。

Inactivation of the Prelimbic Cortex Impairs the Context-Induced Reinstatement of Ethanol Seeking.

作者信息

Palombo Paola, Leao Rodrigo M, Bianchi Paula C, de Oliveira Paulo E C, Planeta Cleopatra da Silva, Cruz Fábio C

机构信息

Laboratory of Pharmacology, School of Pharmaceutical Sciences, Universidade Estadual Paulista, São Paulo, Brazil.

Joint Graduate Program in Physiological Sciences UFSCar/UNESP, São Carlos, Brazil.

出版信息

Front Pharmacol. 2017 Oct 17;8:725. doi: 10.3389/fphar.2017.00725. eCollection 2017.

Abstract

Evidence indicates that drug relapse in humans is often provoked by exposure to the self-administered drug-associated context. An animal model called "ABA renewal procedure" has been used to study the context-induced relapse to drug seeking. Here, we reported a new and feasible training procedure for the ABA renewal method to explore the role of the prelimbic cortex in context-induced relapse to ethanol seeking. By using a saccharin fading technique, we trained rats to self-administer ethanol (10%). The drug delivery was paired with a discrete tone-light cue. Lever pressing was subsequently extinguished in a non-drug-associated context in the presence of the discrete cue. Rats were subsequently tested for reinstatement in contexts A or B, under extinction conditions. Ethanol-associated context induced the reinstatement of ethanol seeking and increased the expression of Fos in the prelimbic cortex. The rate of neural activation in the prelimbic cortex was 3.4% in the extinction context B and 7.7% in the drug-associated context A, as evidenced by double-labeling of Fos and the neuron-specific protein NeuN. The reversible inactivation of the neural activity in the prelimbic cortex with gamma-Aminobutyric acid (GABA) receptor agonists (muscimol + baclofen) attenuated the context-induced reinstatement of ethanol self-administration. These results demonstrated that the neuronal activation of the prelimbic cortex is involved in the context-induced reinstatement of ethanol seeking.

摘要

有证据表明,人类的药物复吸往往是由接触自我给药相关的环境所引发的。一种名为“ABA更新程序”的动物模型已被用于研究环境诱导的觅药行为复发。在此,我们报告了一种用于ABA更新方法的新的可行训练程序,以探究前边缘皮层在环境诱导的乙醇觅药行为复发中的作用。通过使用糖精消退技术,我们训练大鼠自我给药乙醇(10%)。药物递送与离散的声光提示配对。随后,在离散提示存在的情况下,在与药物无关的环境中对压杆行为进行消退训练。随后,在消退条件下,对大鼠在A或B环境中的恢复情况进行测试。与乙醇相关的环境诱导了乙醇觅药行为的恢复,并增加了前边缘皮层中Fos的表达。通过Fos与神经元特异性蛋白NeuN的双重标记证明,前边缘皮层中的神经激活率在消退环境B中为3.4%,在与药物相关的环境A中为7.7%。用γ-氨基丁酸(GABA)受体激动剂(蝇蕈醇+巴氯芬)可逆性失活前边缘皮层中的神经活动,减弱了环境诱导的乙醇自我给药恢复。这些结果表明,前边缘皮层的神经元激活参与了环境诱导的乙醇觅药行为恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9006/5651025/eddf5b769170/fphar-08-00725-g001.jpg

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