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本文引用的文献

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Lithium, but not fluoxetine or the corticotropin-releasing factor receptor 1 receptor antagonist R121919, increases cell proliferation in the adult dentate gyrus.锂,而非氟西汀或促肾上腺皮质激素释放因子受体 1 受体拮抗剂 R121919,可增加成年齿状回的细胞增殖。
J Pharmacol Exp Ther. 2011 Apr;337(1):180-6. doi: 10.1124/jpet.110.175372. Epub 2011 Jan 10.
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Social defeat stress produces prolonged alterations in acoustic startle and body weight gain in male Long Evans rats.社交挫败应激可导致雄性长爪沙鼠的听觉惊跳反应和体重增加出现长时间改变。
J Psychiatr Res. 2010 Jan;44(2):106-11. doi: 10.1016/j.jpsychires.2009.05.005. Epub 2009 Jul 1.
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Alcohol inhibition of neurogenesis: a mechanism of hippocampal neurodegeneration in an adolescent alcohol abuse model.酒精抑制神经发生:青少年酒精滥用模型中海马神经退行性变的一种机制。
Hippocampus. 2010 May;20(5):596-607. doi: 10.1002/hipo.20665.
4
Strain differences in proliferation of progenitor cells in the dentate gyrus of the adult rat and the response to fluoxetine are dependent on corticosterone.成年大鼠齿状回中祖细胞增殖的品系差异以及对氟西汀的反应取决于皮质酮。
Neuroscience. 2008 Dec 2;157(3):677-82. doi: 10.1016/j.neuroscience.2008.08.072. Epub 2008 Sep 27.
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IL-1beta is an essential mediator of the antineurogenic and anhedonic effects of stress.白细胞介素-1β是应激抗神经生成和快感缺失作用的重要介质。
Proc Natl Acad Sci U S A. 2008 Jan 15;105(2):751-6. doi: 10.1073/pnas.0708092105. Epub 2008 Jan 4.
6
Rats selectively-bred for behavior related to affective disorders: proclivity for intake of alcohol and drugs of abuse, and measures of brain monoamines.为与情感障碍相关行为而选择性培育的大鼠:对酒精和滥用药物的摄取倾向以及脑单胺的测量。
Biochem Pharmacol. 2008 Jan 1;75(1):134-59. doi: 10.1016/j.bcp.2007.09.027. Epub 2007 Oct 6.
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Acute psychosocial stress reduces cell survival in adult hippocampal neurogenesis without altering proliferation.急性社会心理应激会降低成年海马神经发生中的细胞存活率,而不会改变细胞增殖。
J Neurosci. 2007 Mar 14;27(11):2734-43. doi: 10.1523/JNEUROSCI.3849-06.2007.
8
Neurogenesis and helplessness are mediated by controllability in males but not in females.神经发生和无助感在雄性中由可控性介导,而在雌性中则不然。
Biol Psychiatry. 2007 Sep 1;62(5):487-95. doi: 10.1016/j.biopsych.2006.10.033. Epub 2007 Feb 16.
9
Expression of fibroblast growth factor-2 and brain-derived neurotrophic factor mRNA in the medial prefrontal cortex and hippocampus after uncontrollable or controllable stress.不可控或可控应激后内侧前额叶皮质和海马中碱性成纤维细胞生长因子-2及脑源性神经营养因子mRNA的表达
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Two genetic rat models of arterial hypertension show different mechanisms by which adult hippocampal neurogenesis is increased.两种动脉高血压的基因大鼠模型显示出成年海马神经发生增加的不同机制。
Dev Neurosci. 2007;29(1-2):124-33. doi: 10.1159/000096217.

多种应激源未能减少成年海马神经发生。

Several stressors fail to reduce adult hippocampal neurogenesis.

机构信息

Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA 30322, United States.

出版信息

Psychoneuroendocrinology. 2011 Nov;36(10):1520-9. doi: 10.1016/j.psyneuen.2011.04.006. Epub 2011 May 19.

DOI:10.1016/j.psyneuen.2011.04.006
PMID:21600697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3185166/
Abstract

Neurogenesis in the dentate gyrus of the hippocampus of adult laboratory animals has been widely reported to be vulnerable to many psychological and physical stressors. However, we have found no effects of acute restraint stress, acute or subchronic tailshock stress, or acute, subchronic, or chronic resident-intruder stress on neural progenitor cell (NPC) proliferation, short or long term survival of newborn cells, or brain-derived neurotrophic factor (BDNF) mRNA expression in adult rats. In addition, we did not observe any effect of chronic resident-intruder stress on NPC proliferation in adolescent rats. A selectively bred stress-sensitive line was also found to exhibit no alterations in NPC proliferation following tailshock stress, although this line did exhibit a lower proliferation rate under baseline (unstressed) conditions when compared with non-selected rats. These results challenge the prevailing hypothesis that any stressor of sufficient intensity and duration has a marked negative impact upon the rate of hippocampal neurogenesis, and suggest that some yet unidentified factors related to stress and experimental conditions are crucial in the regulation of neurogenesis.

摘要

成年实验动物海马齿状回中的神经发生已被广泛报道易受许多心理和生理应激源的影响。然而,我们没有发现急性束缚应激、急性或亚慢性尾部电击应激、急性、亚慢性或慢性群居-入侵应激对成年大鼠神经祖细胞(NPC)增殖、新生细胞的短期或长期存活或脑源性神经营养因子(BDNF)mRNA 表达有任何影响。此外,我们也没有观察到慢性群居-入侵应激对青少年大鼠 NPC 增殖的任何影响。选择性繁殖的应激敏感系也被发现,其在尾部电击应激后 NPC 增殖没有改变,尽管与非选择大鼠相比,该系在基础(无应激)条件下的增殖率较低。这些结果对普遍存在的假设提出了挑战,即任何强度和持续时间足够的应激源都会对海马神经发生的速度产生显著的负面影响,并表明与应激和实验条件有关的一些尚未确定的因素在神经发生的调节中至关重要。