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对苯丙胺的50千赫兹发声反应致敏性差预示着大鼠对该药物自我给药的易感性。

Poor sensitization of 50-kHz vocalization response to amphetamine predicts rat susceptibility to self-administration of the drug.

作者信息

Taracha Ewa, Kaniuga Ewelina, Wyszogrodzka Edyta, Płaźnik Adam, Stefański Roman, Chrapusta Stanisław J

机构信息

Department of Neurochemistry, Institute of Psychiatry and Neurology, 9 Sobieskiego St., 02-957, Warsaw, Poland.

Department of Pharmacology and Physiology of the Nervous System, Institute of Psychiatry and Neurology, 9 Sobieskiego St., 02-957, Warsaw, Poland.

出版信息

Psychopharmacology (Berl). 2016 Jul;233(14):2827-40. doi: 10.1007/s00213-016-4328-4. Epub 2016 Jun 2.

DOI:10.1007/s00213-016-4328-4
PMID:27256355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4917579/
Abstract

RATIONALE

Our previous studies showed promise for using sensitization of the frequency-modulated 50-kHz vocalization response to amphetamine (AMPH) as an index of rat vulnerability to AMPH addiction.

OBJECTIVE

This study aimed to test the utility of sensitizing frequency-modulated (FM) 50-kHz vocalization in the AMPH self-administration paradigm as well as the ability of N-acetylcysteine to prevent self-administration relapse.

METHODS

Rats were subjected to the so-called two-injection protocol of sensitization (TIPS) using AMPH and were categorized as low-sensitized callers (LCTIPS) or high-sensitized callers (HCTIPS) based on the individual outcomes. Then, they were given 44 sessions of AMPH self-administration followed by a 17-session N-acetylcysteine-aided extinction course and a single session of AMPH-primed self-administration reinstatement.

RESULTS

LCTIPS compared to HCTIPS rats showed no considerable difference in the FM 50-kHz vocalization rate during the self-administration training or extinction course, but they were considerably more likely to acquire AMPH self-administration and experience drug-induced reinstatement of this trait. Moreover, the LCTIPS rats were more likely than HCTIPS rats to have a markedly higher FM 50-kHz vocalization rate after AMPH reinstatement. N-acetylcysteine did not affect the course of self-administration extinction or the instrumental or FM 50-kHz vocalization responses to AMPH reinstatement.

CONCLUSIONS

There is no link between the FM 50-kHz vocalization and key characteristics of AMPH self-administration. Additionally, N-acetylcysteine does not help prevent AMPH self-administration relapse. However, there is a high predictive value for poor sensitization of the FM 50-kHz vocalization response to AMPH with respect to the acquisition and maintenance of self-administration of this psychostimulant.

摘要

原理

我们之前的研究表明,利用对苯丙胺(AMPH)的调频50千赫发声反应的敏化作用作为大鼠对AMPH成瘾易感性的指标具有前景。

目的

本研究旨在测试在AMPH自我给药范式中调频(FM)50千赫发声的敏化作用的效用,以及N-乙酰半胱氨酸预防自我给药复发的能力。

方法

使用AMPH对大鼠进行所谓的双注射敏化方案(TIPS),并根据个体结果将其分类为低敏化发声者(LCTIPS)或高敏化发声者(HCTIPS)。然后,让它们进行44次AMPH自我给药实验,随后进行17次N-乙酰半胱氨酸辅助消退疗程以及单次AMPH激发的自我给药复吸实验。

结果

与HCTIPS大鼠相比,LCTIPS大鼠在自我给药训练或消退疗程期间的FM 50千赫发声率没有显著差异,但它们更有可能学会AMPH自我给药并经历药物诱导的该行为复吸。此外,LCTIPS大鼠比HCTIPS大鼠在AMPH激发后更有可能具有明显更高的FM 50千赫发声率。N-乙酰半胱氨酸不影响自我给药消退过程或对AMPH激发的工具性或FM 50千赫发声反应。

结论

FM 50千赫发声与AMPH自我给药的关键特征之间没有关联。此外,N-乙酰半胱氨酸无助于预防AMPH自我给药复发。然而,对于这种精神兴奋剂的自我给药的获得和维持,FM 50千赫发声反应对AMPH的低敏化具有较高的预测价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/bdb896398a02/213_2016_4328_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/8c1c41f0dd7c/213_2016_4328_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/c8650a9db786/213_2016_4328_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/0469f6bc96f5/213_2016_4328_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/e1815dea1d8d/213_2016_4328_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/f06548726669/213_2016_4328_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/bdb896398a02/213_2016_4328_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/8c1c41f0dd7c/213_2016_4328_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/c8650a9db786/213_2016_4328_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/0469f6bc96f5/213_2016_4328_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/e1815dea1d8d/213_2016_4328_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/f06548726669/213_2016_4328_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/4917579/bdb896398a02/213_2016_4328_Fig6_HTML.jpg

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