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本文引用的文献

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Adolescent cocaine self-administration induces habit behavior in adulthood: sex differences and structural consequences.青少年可卡因自我给药会在成年期诱发习惯行为:性别差异及结构后果。
Transl Psychiatry. 2016 Aug 30;6(8):e875. doi: 10.1038/tp.2016.150.
2
Connections of the Mouse Orbitofrontal Cortex and Regulation of Goal-Directed Action Selection by Brain-Derived Neurotrophic Factor.小鼠眶额皮质的连接以及脑源性神经营养因子对目标导向行为选择的调节
Biol Psychiatry. 2017 Feb 15;81(4):366-377. doi: 10.1016/j.biopsych.2015.10.026. Epub 2015 Nov 18.
3
Medial Orbitofrontal Cortex Mediates Outcome Retrieval in Partially Observable Task Situations.内侧眶额皮层介导部分可观察任务情境中的结果检索。
Neuron. 2015 Dec 16;88(6):1268-1280. doi: 10.1016/j.neuron.2015.10.044. Epub 2015 Nov 25.
4
Molecular changes in the medial prefrontal cortex and nucleus accumbens are associated with blocking the behavioral sensitization to cocaine.内侧前额叶皮质和伏隔核中的分子变化与阻断对可卡因的行为敏化有关。
Sci Rep. 2015 Nov 5;5:16172. doi: 10.1038/srep16172.
5
The Contingency of Cocaine Administration Accounts for Structural and Functional Medial Prefrontal Deficits and Increased Adrenocortical Activation.可卡因给药的偶然性导致内侧前额叶结构和功能缺陷以及肾上腺皮质激活增加。
J Neurosci. 2015 Aug 26;35(34):11897-910. doi: 10.1523/JNEUROSCI.4961-14.2015.
6
The BDNF Valine 68 to Methionine Polymorphism Increases Compulsive Alcohol Drinking in Mice That Is Reversed by Tropomyosin Receptor Kinase B Activation.脑源性神经营养因子缬氨酸68位点至甲硫氨酸的多态性增加小鼠强迫性饮酒行为,而原肌球蛋白受体激酶B激活可逆转此行为。
Biol Psychiatry. 2016 Mar 15;79(6):463-73. doi: 10.1016/j.biopsych.2015.06.007. Epub 2015 Jun 12.
7
The Impact of Chronic Early Administration of Psychostimulants on Brain Expression of BDNF and Other Neuroplasticity-Relevant Proteins.慢性早期给予精神兴奋剂对脑源性神经营养因子(BDNF)及其他与神经可塑性相关蛋白表达的影响。
J Mol Neurosci. 2015 Oct;57(2):231-42. doi: 10.1007/s12031-015-0611-9. Epub 2015 Jul 8.
8
Adolescent-onset GABAA α1 silencing regulates reward-related decision making.青少年期开始的GABAA α1沉默调节与奖励相关的决策。
Eur J Neurosci. 2015 Aug;42(4):2114-2121. doi: 10.1111/ejn.12995. Epub 2015 Aug 4.
9
Synaptic Cytoskeletal Plasticity in the Prefrontal Cortex Following Psychostimulant Exposure.精神兴奋剂暴露后前额叶皮质中的突触细胞骨架可塑性
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10
Selective role of the catalytic PI3K subunit p110β in impaired higher order cognition in fragile X syndrome.催化性PI3K亚基p110β在脆性X综合征高阶认知受损中的选择性作用。
Cell Rep. 2015 May 5;11(5):681-8. doi: 10.1016/j.celrep.2015.03.065. Epub 2015 Apr 23.

前额叶皮质脑源性神经营养因子:可卡因和食物强化行为的调控关键。

Prefrontal cortical BDNF: A regulatory key in cocaine- and food-reinforced behaviors.

作者信息

Pitts Elizabeth G, Taylor Jane R, Gourley Shannon L

机构信息

Graduate Program in Neuroscience, Yerkes National Primate Research Center, Emory University, Atlanta, GA, United States.

Department of Psychiatry, Yale University School of Medicine, New Haven, CT, United States; Interdepartmental Neuroscience Program, Department of Psychology, Yale University, New Haven, CT, United States.

出版信息

Neurobiol Dis. 2016 Jul;91:326-35. doi: 10.1016/j.nbd.2016.02.021. Epub 2016 Feb 26.

DOI:10.1016/j.nbd.2016.02.021
PMID:26923993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4913044/
Abstract

Brain-derived neurotrophic factor (BDNF) affects synaptic plasticity and neural structure and plays key roles in learning and memory processes. Recent evidence also points to important, yet complex, roles for BDNF in rodent models of cocaine abuse and addiction. Here we examine the role of prefrontal cortical (PFC) BDNF in reward-related decision making and behavioral sensitivity to, and responding for, cocaine. We focus on BDNF within the medial and orbital PFC, its regulation by cocaine during early postnatal development and in adulthood, and how BDNF in turn influences responding for drug reinforcement, including in reinstatement models. When relevant, we draw comparisons and contrasts with experiments using natural (food) reinforcers. We also summarize findings supporting, or refuting, the possibility that BDNF in the medial and orbital PFC regulate the development and maintenance of stimulus-response habits. Further investigation could assist in the development of novel treatment approaches for cocaine use disorders.

摘要

脑源性神经营养因子(BDNF)影响突触可塑性和神经结构,并在学习和记忆过程中发挥关键作用。最近的证据还表明,BDNF在可卡因滥用和成瘾的啮齿动物模型中起着重要但复杂的作用。在这里,我们研究前额叶皮质(PFC)BDNF在与奖励相关的决策以及对可卡因的行为敏感性和反应中的作用。我们关注内侧和眶额PFC内的BDNF、可卡因在出生后早期发育和成年期对其的调节,以及BDNF如何反过来影响对药物强化的反应,包括在复吸模型中的反应。在相关情况下,我们将使用天然(食物)强化物的实验进行比较和对比。我们还总结了支持或反驳内侧和眶额PFC中的BDNF调节刺激-反应习惯的发展和维持这一可能性的研究结果。进一步的研究可能有助于开发针对可卡因使用障碍的新型治疗方法。