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本文引用的文献

1
The effects of congenital brain serotonin deficiency on responses to chronic fluoxetine.先天性大脑血清素缺乏对慢性氟西汀反应的影响。
Transl Psychiatry. 2013 Aug 13;3(8):e291. doi: 10.1038/tp.2013.65.
2
Paradoxical increase in survival of newborn neurons in the dentate gyrus of mice with constitutive depletion of serotonin.在 5-羟色胺持续耗竭的小鼠齿状回中新生神经元的存活率出现矛盾性增加。
Eur J Neurosci. 2013 Sep;38(5):2650-8. doi: 10.1111/ejn.12297. Epub 2013 Jul 10.
3
The effects of brain serotonin deficiency on behavioural disinhibition and anxiety-like behaviour following mild early life stress.轻度早期生活应激后大脑 5-羟色胺缺乏对行为抑制和焦虑样行为的影响。
Int J Neuropsychopharmacol. 2013 Oct;16(9):2081-94. doi: 10.1017/S1461145713000321. Epub 2013 May 14.
4
Cortical control of affective networks.皮质对情感网络的控制。
J Neurosci. 2013 Jan 16;33(3):1116-29. doi: 10.1523/JNEUROSCI.0092-12.2013.
5
The 5-HT deficiency theory of depression: perspectives from a naturalistic 5-HT deficiency model, the tryptophan hydroxylase 2Arg439His knockin mouse.抑郁症 5-HT 缺乏理论:来自天然 5-HT 缺乏模型,色氨酸羟化酶 2Arg439His 基因敲入小鼠的观点。
Philos Trans R Soc Lond B Biol Sci. 2012 Sep 5;367(1601):2444-59. doi: 10.1098/rstb.2012.0109.
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Differential environmental regulation of neurogenesis along the septo-temporal axis of the hippocampus.海马沿隔颞轴的神经发生的差异环境调节。
Neuropharmacology. 2012 Sep;63(3):374-84. doi: 10.1016/j.neuropharm.2012.04.022. Epub 2012 Apr 28.
7
Investigating anxiety and depressive-like phenotypes in genetic mouse models of serotonin depletion.研究 5-羟色胺耗竭的遗传小鼠模型中的焦虑和抑郁样表型。
Neuropharmacology. 2012 Jan;62(1):144-54. doi: 10.1016/j.neuropharm.2011.08.049. Epub 2011 Sep 21.
8
The neurogenesis hypothesis of affective and anxiety disorders: are we mistaking the scaffolding for the building?情感和焦虑障碍的神经发生假说:我们是否把脚手架误认为是建筑物?
Neuropharmacology. 2012 Jan;62(1):21-34. doi: 10.1016/j.neuropharm.2011.09.003. Epub 2011 Sep 19.
9
Several stressors fail to reduce adult hippocampal neurogenesis.多种应激源未能减少成年海马神经发生。
Psychoneuroendocrinology. 2011 Nov;36(10):1520-9. doi: 10.1016/j.psyneuen.2011.04.006. Epub 2011 May 19.
10
Deficient serotonin neurotransmission and depression-like serotonin biomarker alterations in tryptophan hydroxylase 2 (Tph2) loss-of-function mice.色氨酸羟化酶 2(Tph2)功能丧失型小鼠中血清素神经递质传递不足和类似抑郁的血清素生物标志物改变。
Mol Psychiatry. 2012 Jul;17(7):694-704. doi: 10.1038/mp.2011.50. Epub 2011 May 3.

慢性轻度应激和先天性 5-羟色胺缺乏症反应中的性别差异。

Sex differences in response to chronic mild stress and congenital serotonin deficiency.

机构信息

Department of Cell Biology, Duke University, Durham, NC 27710, USA.

Department of Cell Biology, Duke University, Durham, NC 27710, USA; Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Psychoneuroendocrinology. 2014 Feb;40:123-9. doi: 10.1016/j.psyneuen.2013.11.008. Epub 2013 Nov 19.

DOI:10.1016/j.psyneuen.2013.11.008
PMID:24485484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3918518/
Abstract

Women exhibit a nearly twofold increased risk of developing depression and anxiety disorders when compared to men, a fact that has been hypothesized to result in part from increased stress susceptibility. Here, we used the tryptophan hydroxylase-2 R439H knock-in mouse (Tph2KI) and the chronic unpredictable mild stress (CMS) model to examine sex differences in response to congenital 5-HT deficiency and chronic stress. Our results demonstrate that female mice, but not 5-HT-deficient animals, exhibit significantly increased susceptibility to CMS-induced despair-like behavior in the forced swim test. In addition, female 5-HT-deficient mice exhibit anhedonia-like behavior in the sucrose preference test, whereas male 5-HT-deficient animals do not, suggesting that females exhibit increased sensitivity to at least some of the effects of congenital 5-HT deficiency. Although CMS did not reduce cell proliferation in the hippocampus, low levels of brain 5-HT were associated with increased hippocampal cell proliferation, an effect that was predominantly observed in females. Overall, these results highlight the importance of interactions between psychiatric disease risk factors such as sex, chronic stress and congenital 5-HT deficiency in the development of aberrant emotional behavior.

摘要

与男性相比,女性患抑郁症和焦虑症的风险几乎增加了两倍,这一事实部分归因于女性更容易受到压力的影响。在这里,我们使用色氨酸羟化酶-2 R439H 敲入小鼠(Tph2KI)和慢性不可预测轻度应激(CMS)模型来检查先天性 5-HT 缺乏和慢性应激对反应的性别差异。我们的结果表明,与 5-HT 缺乏动物相比,雌性小鼠对 CMS 诱导的强迫游泳试验中的绝望样行为表现出明显更高的易感性。此外,雌性 5-HT 缺乏小鼠在蔗糖偏好试验中表现出快感缺失样行为,而雄性 5-HT 缺乏动物则没有,这表明雌性对至少一些先天性 5-HT 缺乏的影响表现出更高的敏感性。尽管 CMS 并未减少海马中的细胞增殖,但大脑中 5-HT 水平较低与海马细胞增殖增加有关,这种作用主要发生在女性中。总体而言,这些结果强调了精神疾病风险因素(如性别、慢性应激和先天性 5-HT 缺乏)之间的相互作用在异常情绪行为发展中的重要性。