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本文引用的文献

1
Orexin mediates morphine place preference, but not morphine-induced hyperactivity or sensitization.食欲素调节吗啡诱导的奖赏效应,但不调节吗啡诱导的活动过度或敏化。
Brain Res. 2010 Mar 4;1317:24-32. doi: 10.1016/j.brainres.2009.12.035. Epub 2009 Dec 23.
2
Electrophysiological effects of orexin/hypocretin on nucleus accumbens shell neurons in rats: an in vitro study.食欲素/下丘脑泌素对大鼠伏隔核壳部神经元的电生理效应:一项体外研究
Peptides. 2009 Aug;30(8):1487-96. doi: 10.1016/j.peptides.2009.04.018. Epub 2009 May 4.
3
Reinstatement of cocaine seeking by hypocretin (orexin) in the ventral tegmental area: independence from the local corticotropin-releasing factor network.腹侧被盖区中下丘脑泌素(食欲素)对可卡因觅求行为的恢复作用:独立于局部促肾上腺皮质激素释放因子网络
Biol Psychiatry. 2009 May 15;65(10):857-62. doi: 10.1016/j.biopsych.2009.01.018. Epub 2009 Feb 28.
4
Insular hypocretin transmission regulates nicotine reward.岛叶下丘泌素传递调节尼古丁奖赏。
Proc Natl Acad Sci U S A. 2008 Dec 9;105(49):19480-5. doi: 10.1073/pnas.0808023105. Epub 2008 Nov 24.
5
Hypocretin /orexin preferentially activates caudomedial ventral tegmental area dopamine neurons.下丘脑泌素/食欲素优先激活尾内侧腹侧被盖区多巴胺能神经元。
Eur J Neurosci. 2008 Oct;28(8):1629-40. doi: 10.1111/j.1460-9568.2008.06453.x.
6
Activation of orexin/hypocretin projections to basal forebrain and paraventricular thalamus by acute nicotine.急性尼古丁对投射至基底前脑和室旁丘脑的食欲素/下丘脑泌素神经纤维的激活作用。
Brain Res Bull. 2008 Dec 16;77(6):367-73. doi: 10.1016/j.brainresbull.2008.09.014. Epub 2008 Oct 23.
7
Role of lateral hypothalamic orexin neurons in reward processing and addiction.外侧下丘脑食欲素神经元在奖赏处理和成瘾中的作用。
Neuropharmacology. 2009;56 Suppl 1(Suppl 1):112-21. doi: 10.1016/j.neuropharm.2008.06.060. Epub 2008 Jul 4.
8
Effects of cocaine place conditioning, chronic escalating-dose "binge" pattern cocaine administration and acute withdrawal on orexin/hypocretin and preprodynorphin gene expressions in lateral hypothalamus of Fischer and Sprague-Dawley rats.可卡因位置条件反射、慢性递增剂量“ binge”模式可卡因给药及急性戒断对Fischer和Sprague-Dawley大鼠下丘脑外侧区食欲素/下丘脑泌素及前强啡肽原基因表达的影响
Neuroscience. 2008 Jun 2;153(4):1225-34. doi: 10.1016/j.neuroscience.2008.03.023. Epub 2008 Mar 22.
9
Orexin mediates the expression of precipitated morphine withdrawal and concurrent activation of the nucleus accumbens shell.食欲素介导戒断诱发的吗啡戒断反应的表达以及伏隔核壳的同时激活。
Biol Psychiatry. 2008 Aug 1;64(3):175-83. doi: 10.1016/j.biopsych.2008.03.006. Epub 2008 Apr 18.
10
Differential effects of the hypocretin 1 receptor antagonist SB 334867 on high-fat food self-administration and reinstatement of food seeking in rats.下丘脑泌素1受体拮抗剂SB 334867对大鼠高脂食物自我给药及食物寻求行为恢复的不同影响。
Br J Pharmacol. 2008 May;154(2):406-16. doi: 10.1038/bjp.2008.3. Epub 2008 Jan 28.

食欲素/下丘脑分泌素在成瘾中的作用。

Role of orexin/hypocretin in dependence and addiction.

机构信息

Department of Psychiatry, Ribicoff Research Facilities, Yale University School of Medicine, New Haven, CT 06508, USA.

出版信息

Brain Res. 2010 Feb 16;1314:130-8. doi: 10.1016/j.brainres.2009.08.028. Epub 2009 Aug 20.

DOI:10.1016/j.brainres.2009.08.028
PMID:19699189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2819591/
Abstract

The orexins (or hypocretins) are hypothalamic neuropeptides that have been implicated in a variety of behaviors ranging from feeding to sleep and arousal. Evidence from animal models suggests a role for orexins in reward processing and drug addiction. In this review, we discuss orexin's interaction with the mesocorticolimbic reward pathway and the effects of drugs of abuse on the orexin system. We further review models of drug dependence and addiction and describe behavioral alterations that are seen when the orexin system is manipulated both pharmacologically and genetically. Based on the findings reported in the literature thus far, we posit that orexin functioning contributes to both drug reward and drug-related stress/aversive responsiveness; however, diverse anatomical substrates, and perhaps receptor specificity, contribute differentially to reward and stress components.

摘要

食欲素(或下丘脑泌素)是下丘脑神经肽,与从进食到睡眠和觉醒等各种行为有关。动物模型的证据表明,食欲素在奖励处理和药物成瘾中起作用。在这篇综述中,我们讨论了食欲素与中脑边缘奖赏通路的相互作用,以及滥用药物对食欲素系统的影响。我们进一步回顾了药物依赖和成瘾的模型,并描述了在药理学和遗传学上操纵食欲素系统时观察到的行为改变。基于迄今为止文献中的发现,我们假设食欲素的功能有助于药物奖励和与药物相关的应激/厌恶反应;然而,不同的解剖学基础,也许还有受体特异性,对奖励和应激成分的贡献不同。