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Biol Psychiatry. 2006 Jun 15;59(12):1116-27. doi: 10.1016/j.biopsych.2006.02.013. Epub 2006 Apr 21.
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Endogenous opioids upregulate brain-derived neurotrophic factor mRNA through delta- and micro-opioid receptors independent of antidepressant-like effects.内源性阿片肽通过δ-阿片受体和微小阿片受体上调脑源性神经营养因子mRNA,且与抗抑郁样效应无关。
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Signaling pathways regulating gene expression, neuroplasticity, and neurotrophic mechanisms in the action of antidepressants: a critical overview.抗抑郁药作用中调节基因表达、神经可塑性和神经营养机制的信号通路:批判性综述。
Pharmacol Rev. 2006 Mar;58(1):115-34. doi: 10.1124/pr.58.1.7.
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What is the biological significance of BDNF mRNA targeting in the dendrites? Clues from epilepsy and cortical development.脑源性神经营养因子信使核糖核酸在树突中的靶向作用的生物学意义是什么?来自癫痫和皮质发育的线索。
Mol Neurobiol. 2006 Feb;33(1):17-32. doi: 10.1385/MN:33:1:017.
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The dynamic relationship between mu and kappa opioid receptors in body temperature regulation.μ和κ阿片受体在体温调节中的动态关系。
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6
Depressive-like effects of the kappa-opioid receptor agonist salvinorin A on behavior and neurochemistry in rats.κ-阿片受体激动剂沙维诺林A对大鼠行为和神经化学的抑郁样作用。
J Pharmacol Exp Ther. 2006 Jan;316(1):440-7. doi: 10.1124/jpet.105.092304. Epub 2005 Oct 13.
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The effect of escitalopram, desipramine, electroconvulsive seizures and lithium on brain-derived neurotrophic factor mRNA and protein expression in the rat brain and the correlation to 5-HT and 5-HIAA levels.艾司西酞普兰、地昔帕明、电惊厥发作及锂盐对大鼠脑源性神经营养因子mRNA和蛋白表达的影响及其与5-羟色胺和5-羟吲哚乙酸水平的相关性
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Stress increases dynorphin immunoreactivity in limbic brain regions and dynorphin antagonism produces antidepressant-like effects.应激会增加边缘脑区强啡肽的免疫反应性,且强啡肽拮抗作用会产生类抗抑郁效应。
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Depression: a case of neuronal life and death?抑郁症:一个关于神经元生死的案例?
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中枢κ-阿片受体介导的诺-纳洛酮啡肽的抗抑郁样作用:行为学和脑源性神经营养因子mRNA表达研究。

Central kappa-opioid receptor-mediated antidepressant-like effects of nor-Binaltorphimine: behavioral and BDNF mRNA expression studies.

作者信息

Zhang Huina, Shi Yong-Gong, Woods James H, Watson Stanley J, Ko Mei-Chuan

机构信息

Department of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.

出版信息

Eur J Pharmacol. 2007 Sep 10;570(1-3):89-96. doi: 10.1016/j.ejphar.2007.05.045. Epub 2007 Jun 9.

DOI:10.1016/j.ejphar.2007.05.045
PMID:17601558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2031926/
Abstract

kappa-opioid receptor antagonists such as nor-Binaltorphimine (nor-BNI) have been shown to produce antidepressant-like behavioral effects in animal models of depression. The aim of this study was to investigate further the duration of centrally administered nor-BNI-induced antidepressant-like actions measured by both behavior and brain-derived neurotrophic factor (BDNF) gene expression. In addition, antagonist studies were conducted to determine the role of opioid receptor subtypes and the time course of nor-BNI's pharmacological actions. Antidepressant-like behavioral effects were measured by decreased immobility in the rat forced swim test and BDNF mRNA expression was determined by in situ hybridization. Centrally administered nor-BNI (20 microg, i.c.v.) decreased immobility and increased BDNF mRNA expression in the hippocampus on day 1, not on days 3-14, post-administration. Systemic administration of selective mu-, delta- and kappa-opioid receptor antagonists did not block nor-BNI-induced antidepressant-like effects. In contrast, i.c.v. administration of nor-BNI 7 or 14 days earlier significantly blocked subsequent nor-BNI-induced decreased immobility and upregulation of BDNF mRNA expression. Although the duration of nor-BNI's antidepressant-like effects did not synchronize with that of its kappa-opioid receptor antagonist effects, this study is the first to show that centrally administered nor-BNI, like most clinically used antidepressants, can upregulate BDNF mRNA expression in the rat hippocampus. These findings further demonstrate that central kappa-opioid receptor mediates antidepressant-like effects of nor-BNI measured by both behavior and BDNF gene expression.

摘要

κ-阿片受体拮抗剂,如去甲二丙诺啡(nor-BNI),已被证明在抑郁症动物模型中可产生类抗抑郁行为效应。本研究的目的是进一步探究通过行为和脑源性神经营养因子(BDNF)基因表达测量的中枢给予nor-BNI诱导的类抗抑郁作用的持续时间。此外,进行拮抗剂研究以确定阿片受体亚型的作用以及nor-BNI药理作用的时间进程。通过大鼠强迫游泳试验中不动时间的减少来测量类抗抑郁行为效应,并通过原位杂交确定BDNF mRNA表达。中枢给予nor-BNI(20微克,脑室内注射)在给药后第1天可减少不动时间并增加海马体中BDNF mRNA表达,而在第3 - 14天则无此作用。全身给予选择性μ-、δ-和κ-阿片受体拮抗剂并未阻断nor-BNI诱导的类抗抑郁效应。相反,提前7天或14天脑室内注射nor-BNI可显著阻断随后nor-BNI诱导的不动时间减少和BDNF mRNA表达上调。尽管nor-BNI的类抗抑郁效应持续时间与其κ-阿片受体拮抗剂效应的持续时间不同步,但本研究首次表明,与大多数临床使用的抗抑郁药一样,中枢给予nor-BNI可上调大鼠海马体中BDNF mRNA表达。这些发现进一步证明,中枢κ-阿片受体介导了通过行为和BDNF基因表达测量的nor-BNI的类抗抑郁效应。