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本文引用的文献

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Recent Perspectives on Sex Differences in Compulsion-Like and Binge Alcohol Drinking.近期对强迫性和 binge 饮酒行为中的性别差异的观点看法。
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The contribution of medium spiny neuron subtypes in the nucleus accumbens core to compulsive-like ethanol drinking.伏隔核核心中型棘神经元亚型在强迫性样乙醇摄入中的作用。
Neuropharmacology. 2021 Apr 1;187:108497. doi: 10.1016/j.neuropharm.2021.108497. Epub 2021 Feb 11.
3
Three Weeks of Binge Alcohol Drinking Generates Increased Alcohol Front-Loading and Robust Compulsive-Like Alcohol Drinking in Male and Female C57BL/6J Mice. binge alcohol drinking 是豪饮 binge drinking 的名词形式,因此,译文“Three Weeks of Binge Alcohol Drinking”可处理为“连续三周豪饮酒精”。此外,原文中的“front-loading”通常被翻译为“前置加载”,但结合语境,这里指的是“饮酒量前置增加”,因此,译文将其处理为“饮酒量前置增加”。 综上,译文为: 连续三周豪饮酒精可导致雄性和雌性 C57BL/6J 小鼠酒精摄入量前置增加和强迫性觅酒行为增强。
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4
Aversion-resistant fentanyl self-administration in mice.耐阿片类药物的芬太尼自我给药在小鼠体内的研究
Psychopharmacology (Berl). 2021 Mar;238(3):699-710. doi: 10.1007/s00213-020-05722-6. Epub 2020 Nov 23.
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Fentanyl vapor self-administration model in mice to study opioid addiction.在小鼠中进行芬太尼蒸气自我给药模型以研究阿片类药物成瘾。
Sci Adv. 2020 Aug 5;6(32):eabc0413. doi: 10.1126/sciadv.abc0413. eCollection 2020 Aug.
6
The Endocrine System and Alcohol Drinking in Females.女性的内分泌系统与饮酒行为。
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7
Validation of a nicotine vapor self-administration model in rats with relevance to electronic cigarette use.一种与电子烟使用相关的大鼠尼古丁蒸气自我给药模型的验证
Neuropsychopharmacology. 2020 Oct;45(11):1909-1919. doi: 10.1038/s41386-020-0734-8. Epub 2020 Jun 16.
8
Estrogen Receptor α Regulates Ethanol Excitation of Ventral Tegmental Area Neurons and Binge Drinking in Female Mice.雌激素受体 α 调节腹侧被盖区神经元对乙醇的兴奋作用及雌性小鼠的 binge drinking 行为。
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Increased Responding for Alcohol and Resistance to Aversion in Female Mice.雌性小鼠对酒精的反应增强和对厌恶的抵抗。
Alcohol Clin Exp Res. 2020 Jul;44(7):1400-1409. doi: 10.1111/acer.14384. Epub 2020 Jun 18.
10
Sex bias and omission in neuroscience research is influenced by research model and journal, but not reported NIH funding.神经科学研究中的性别偏见和遗漏受研究模型和期刊的影响,但不受 NIH 资助的影响。
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研究成瘾行为的啮齿动物模型中的性别差异。

Studying Sex Differences in Rodent Models of Addictive Behavior.

机构信息

Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio.

出版信息

Curr Protoc. 2021 Apr;1(4):e119. doi: 10.1002/cpz1.119.

DOI:10.1002/cpz1.119
PMID:33901344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8208026/
Abstract

Animal models of addictive behaviors are useful for uncovering neural mechanisms involved in the development of dependence and for identifying risk factors for drug abuse. One such risk factor is biological sex, which strongly moderates drug self-administration behavior in rodents. Female rodents are more likely to acquire drug self-administration behaviors, consume higher amounts of drug, and reinstate drug-seeking behavior more readily. Despite this female vulnerability, preclinical addiction research has largely been done in male animals. The study of sex differences in rodent models of addictive behavior is increasing, however, as more investigators are choosing to include both male and female animals in experiments. This commentary is meant to serve as an introductory guide for preclinical investigators new to the study of sex differences in addiction. We provide an overview of self-administration models, a broad view of female versus male self-administration behaviors, and suggestions for study design and implementation. Inclusion of female subjects in preclinical addiction research is timely, as problem drug and alcohol use in women is increasing. With proper attention, design, and analysis, the study of sex differences in addiction has the potential to uncover novel neural mechanisms and lead to greater translational success for addiction research. © 2021 Wiley Periodicals LLC.

摘要

动物成瘾行为模型对于揭示成瘾发展过程中的神经机制以及确定药物滥用的风险因素非常有用。其中一个风险因素是生物性别,它强烈调节啮齿动物的药物自我给药行为。雌性啮齿动物更有可能获得药物自我给药行为,消耗更多的药物,并更易重新开始寻找药物。尽管存在这种女性易感性,但临床前成瘾研究主要在雄性动物中进行。然而,随着越来越多的研究人员选择在实验中同时纳入雄性和雌性动物,对成瘾行为的啮齿动物模型中性别差异的研究正在增加。本文旨在为刚开始研究成瘾性别差异的临床前研究人员提供一个入门指南。我们提供了自我给药模型概述、雌性与雄性自我给药行为的广泛比较,以及研究设计和实施的建议。将女性研究对象纳入临床前成瘾研究是及时的,因为女性中与毒品和酒精有关的问题正在增加。通过适当的关注、设计和分析,对成瘾性别差异的研究有可能揭示新的神经机制,并为成瘾研究带来更大的转化成功。© 2021 Wiley Periodicals LLC.