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Why Optogenetics Needs in Vivo Neurochemistry.为什么光遗传学需要活体神经化学。
ACS Chem Neurosci. 2015 Jul 15;6(7):948-50. doi: 10.1021/acschemneuro.5b00003. Epub 2015 May 7.
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Chronic intermittent ethanol exposure reduces presynaptic dopamine neurotransmission in the mouse nucleus accumbens.慢性间歇性乙醇暴露会降低小鼠伏隔核中的突触前多巴胺神经传递。
Drug Alcohol Depend. 2015 May 1;150:24-30. doi: 10.1016/j.drugalcdep.2015.01.019. Epub 2015 Feb 16.
3
Optogenetic stimulation of VTA dopamine neurons reveals that tonic but not phasic patterns of dopamine transmission reduce ethanol self-administration.对腹侧被盖区多巴胺能神经元进行光遗传学刺激发现,多巴胺传递的持续性而非相位性模式会减少乙醇自我给药行为。
Front Behav Neurosci. 2013 Nov 26;7:173. doi: 10.3389/fnbeh.2013.00173. eCollection 2013.
4
Addiction is a Reward Deficit and Stress Surfeit Disorder.成瘾是一种奖励缺失和应激过剩障碍。
Front Psychiatry. 2013 Aug 1;4:72. doi: 10.3389/fpsyt.2013.00072. eCollection 2013.
5
Adenosine signaling in striatal circuits and alcohol use disorders.纹状体回路中的腺苷信号与酒精使用障碍。
Mol Cells. 2013 Sep;36(3):195-202. doi: 10.1007/s10059-013-0192-9. Epub 2013 Aug 1.
6
Cortical activation of accumbens hyperpolarization-active NMDARs mediates aversion-resistant alcohol intake.伏隔核去极化激活型 NMDAR 皮层激活介导了抵抗性酒精摄入。
Nat Neurosci. 2013 Aug;16(8):1094-100. doi: 10.1038/nn.3445. Epub 2013 Jun 30.
7
A causal link between prediction errors, dopamine neurons and learning.预测误差、多巴胺神经元和学习之间的因果关系。
Nat Neurosci. 2013 Jul;16(7):966-73. doi: 10.1038/nn.3413. Epub 2013 May 26.
8
Recombinase-driver rat lines: tools, techniques, and optogenetic application to dopamine-mediated reinforcement.重组酶驱动大鼠品系:工具、技术及光遗传学在多巴胺介导的强化中的应用
Neuron. 2011 Dec 8;72(5):721-33. doi: 10.1016/j.neuron.2011.10.028.
9
Optogenetic interrogation of dopaminergic modulation of the multiple phases of reward-seeking behavior.光遗传学检测多巴胺能调制对寻求奖赏行为多个阶段的影响。
J Neurosci. 2011 Jul 27;31(30):10829-35. doi: 10.1523/JNEUROSCI.2246-11.2011.
10
Evidence that vasopressin V1b receptors mediate the transition to excessive drinking in ethanol-dependent rats.证据表明,血管加压素 V1b 受体介导了乙醇依赖大鼠向过度饮酒的转变。
Addict Biol. 2012 Jan;17(1):76-85. doi: 10.1111/j.1369-1600.2010.00291.x. Epub 2011 Feb 11.

探索酒精成瘾相关行为的神经化学基础:转化研究。

Exploring the Neurochemical Basis of Alcohol Addiction-Related Behaviors: Translational Research.

作者信息

Budygin E A, Weiner J L

机构信息

Wake Forest School of Medicine, USA; Institute of Translational Biomedicine, St. Petersburg State University St. Petersburg, 199034, Russia.

Wake Forest School of Medicine, USA.

出版信息

Transl Biomed. 2015;6(Suppl Spec).

PMID:26770883
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4710378/
Abstract

This Editorial presents the position that translational research continues to play a vital role in the field of alcohol addiction research. Using diverse animal models that mimic fundamental features of the disease, tremendous progress has been made in our understanding of alcohol actions in the brain and in identifying key neurobiological adaptations that may contribute to the pathophysiology of alcohol addiction. Current translational research in this field is now focusing on identifying the causal mechanisms that drive the shift from recreational to abusive ethanol drinking behaviors. The relatively recent development and application of optogenetic and chemogenetic techniques is beginning to afford alcohol researchers with the opportunity to identify specific neuronal circuits that govern key elements of the addiction process. These advances are rapidly pointing the way toward novel neural targets for the development of more effective treatments for addictive disorders.

摘要

本社论提出的观点是,转化研究在酒精成瘾研究领域继续发挥着至关重要的作用。通过使用模拟该疾病基本特征的多种动物模型,我们在理解酒精在大脑中的作用以及确定可能导致酒精成瘾病理生理学的关键神经生物学适应性方面取得了巨大进展。该领域当前的转化研究现在聚焦于确定促使从娱乐性饮酒转变为滥用乙醇饮酒行为的因果机制。光遗传学和化学遗传学技术相对较新的发展与应用,正开始为酒精研究人员提供机会,以识别控制成瘾过程关键要素的特定神经回路。这些进展正迅速为开发更有效的成瘾性疾病治疗方法指明通往新神经靶点的道路。

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