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本文引用的文献

1
Neurobiological Correlates of Pain Avoidance-Like Behavior in Morphine-Dependent and Non-Dependent Rats.吗啡依赖和非依赖大鼠的疼痛回避样行为的神经生物学相关性。
Neuroscience. 2017 Dec 16;366:1-14. doi: 10.1016/j.neuroscience.2017.09.055. Epub 2017 Oct 9.
2
Reward, motivation, and emotion of pain and its relief.疼痛及缓解的奖赏、动机和情绪。
Pain. 2017 Apr;158 Suppl 1(Suppl 1):S43-S49. doi: 10.1097/j.pain.0000000000000798.
3
A Trigger for Opioid Misuse: Chronic Pain and Stress Dysregulate the Mesolimbic Pathway and Kappa Opioid System.阿片类药物滥用的一个触发因素:慢性疼痛和压力使中脑边缘通路和κ阿片系统失调。
Front Neurosci. 2016 Nov 7;10:480. doi: 10.3389/fnins.2016.00480. eCollection 2016.
4
Withdrawal from Chronic Nicotine Exposure Produces Region-Specific Tolerance to Alcohol-Stimulated GluA1 Phosphorylation.慢性尼古丁暴露戒断会产生对酒精刺激的GluA1磷酸化的区域特异性耐受性。
Alcohol Clin Exp Res. 2016 Dec;40(12):2537-2547. doi: 10.1111/acer.13258. Epub 2016 Oct 31.
5
Mechanical Conflict System: A Novel Operant Method for the Assessment of Nociceptive Behavior.机械冲突系统:一种评估伤害性感受行为的新型操作性方法。
PLoS One. 2016 Feb 25;11(2):e0150164. doi: 10.1371/journal.pone.0150164. eCollection 2016.
6
Chronic intermittent voluntary alcohol drinking induces hyperalgesia in Sprague-Dawley rats.慢性间歇性自愿饮酒会导致Sprague-Dawley大鼠出现痛觉过敏。
Int J Physiol Pathophysiol Pharmacol. 2015 Dec 13;7(3):136-44. eCollection 2015.
7
Reinforcement principles for addiction medicine; from recreational drug use to psychiatric disorder.成瘾医学的强化原则;从娱乐性药物使用到精神疾病。
Prog Brain Res. 2016;223:63-76. doi: 10.1016/bs.pbr.2015.07.005. Epub 2015 Oct 1.
8
Intra-cerebral and intra-nasal melanocortin-4 receptor antagonist blocks withdrawal hyperalgesia in alcohol-dependent rats.脑内和鼻内黑素皮质素-4受体拮抗剂可阻断酒精依赖大鼠的戒断性痛觉过敏。
Addict Biol. 2017 May;22(3):692-701. doi: 10.1111/adb.12360. Epub 2016 Jan 24.
9
Brain Circuits Encoding Reward from Pain Relief.编码疼痛缓解奖励的脑回路
Trends Neurosci. 2015 Nov;38(11):741-750. doi: 10.1016/j.tins.2015.09.003.
10
Compulsive-like responding for opioid analgesics in rats with extended access.长期接触阿片类镇痛药的大鼠出现类似强迫性的反应。
Neuropsychopharmacology. 2015 Jan;40(2):421-8. doi: 10.1038/npp.2014.188. Epub 2014 Jul 25.

测量药物依赖大鼠的类似疼痛回避行为。

Measuring Pain Avoidance-Like Behavior in Drug-Dependent Rats.

作者信息

Pahng Amanda R, Edwards Scott

机构信息

Department of Physiology, Louisiana State University Health Sciences Center, New Orleans, Louisiana.

Alcohol & Drug Abuse Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, Louisiana.

出版信息

Curr Protoc Neurosci. 2018 Oct;85(1):e53. doi: 10.1002/cpns.53. Epub 2018 Sep 24.

DOI:10.1002/cpns.53
PMID:30248240
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6175615/
Abstract

In contrast to their analgesic properties, excessive use of either opioids or alcohol produces a paradoxical emergence of heightened pain sensitivity to noxious stimuli, termed hyperalgesia, which may promote increased use of opioids or alcohol drinking to manage worsening pain symptoms. Hyperalgesia has traditionally been measured in rodents via reflex-based assays, including the von Frey method. To better model the motivational and affective dimensions of pain in a state of opioid/alcohol dependence and withdrawal, this unit describes the use of a non-reflex-based method for measuring pain avoidance-like behavior in dependent rats. In the mechanical conflict-avoidance task, rats run across probes of varying heights to avoid a bright aversive light and to reach a dark goal chamber. A longer latency to exit onto the nociceptive probes reflects increased pain avoidance-like behavior during withdrawal. Mechanical conflict-avoidance testing can be repeated to provide both baseline assessment of pain avoidance behavior and pain avoidance measures after the induction of dependence.© 2018 by John Wiley & Sons, Inc.

摘要

与它们的镇痛特性相反,过量使用阿片类药物或酒精会产生一种矛盾的现象,即对有害刺激的疼痛敏感性增强,称为痛觉过敏,这可能会促使人们增加使用阿片类药物或饮酒来控制不断恶化的疼痛症状。传统上,痛觉过敏是通过基于反射的试验在啮齿动物中进行测量的,包括von Frey方法。为了更好地模拟阿片类药物/酒精依赖和戒断状态下疼痛的动机和情感维度,本单元描述了一种基于非反射的方法,用于测量依赖大鼠的疼痛回避样行为。在机械冲突回避任务中,大鼠穿过不同高度的探针,以避免明亮的厌恶性光线并到达黑暗的目标室。退出到伤害性探针上的潜伏期延长反映了戒断期间疼痛回避样行为的增加。可以重复进行机械冲突回避测试,以提供疼痛回避行为的基线评估以及诱导依赖后的疼痛回避测量。© 2018 John Wiley & Sons, Inc.