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本文引用的文献

1
Altered HDAC5 and CREB mRNA expressions in the peripheral leukocytes of major depression.重度抑郁症患者外周血白细胞中HDAC5和CREB mRNA表达的改变
Prog Neuropsychopharmacol Biol Psychiatry. 2007 Apr 13;31(3):628-32. doi: 10.1016/j.pnpbp.2006.12.014. Epub 2006 Dec 28.
2
Chronic antidepressant treatment selectively increases expression of plasticity-related proteins in the hippocampus and medial prefrontal cortex of the rat.慢性抗抑郁药治疗选择性地增加大鼠海马体和内侧前额叶皮质中可塑性相关蛋白的表达。
Neuroscience. 2007 Jan 5;144(1):368-74. doi: 10.1016/j.neuroscience.2006.08.069. Epub 2006 Oct 13.
3
Cyclic AMP response element-binding protein in post-mortem brain of teenage suicide victims: specific decrease in the prefrontal cortex but not the hippocampus.青少年自杀受害者尸检大脑中的环磷酸腺苷反应元件结合蛋白:前额叶皮质有特异性减少,而海马体未出现。
Int J Neuropsychopharmacol. 2007 Oct;10(5):621-9. doi: 10.1017/S1461145706007231. Epub 2006 Sep 18.
4
The many faces of CREB.CREB的多种面貌。
Trends Neurosci. 2005 Aug;28(8):436-45. doi: 10.1016/j.tins.2005.06.005.
5
Alterations in cell adhesion molecule L1 and functionally related genes in major depression: a postmortem study.重度抑郁症中细胞粘附分子L1及功能相关基因的改变:一项尸检研究
Biol Psychiatry. 2005 Apr 1;57(7):716-25. doi: 10.1016/j.biopsych.2004.12.016.
6
Selective phosphorylation of nuclear CREB by fluoxetine is linked to activation of CaM kinase IV and MAP kinase cascades.氟西汀对细胞核内CREB的选择性磷酸化作用与钙调蛋白激酶IV及丝裂原活化蛋白激酶级联反应的激活有关。
Neuropsychopharmacology. 2004 Oct;29(10):1831-40. doi: 10.1038/sj.npp.1300488.
7
Amygdala cyclic adenosine monophosphate response element binding protein phosphorylation in patients with mood disorders: effects of diagnosis, suicide, and drug treatment.情绪障碍患者杏仁核环磷酸腺苷反应元件结合蛋白的磷酸化:诊断、自杀及药物治疗的影响
Biol Psychiatry. 2004 Mar 15;55(6):570-7. doi: 10.1016/j.biopsych.2003.10.023.
8
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
9
Expression of cAMP response element-binding protein in major depression before and after antidepressant treatment.抗抑郁治疗前后重度抑郁症中cAMP反应元件结合蛋白的表达
Neuropsychobiology. 2003;48(4):182-5. doi: 10.1159/000074635.
10
Reduced phosphorylation of cyclic AMP-responsive element binding protein in the postmortem orbitofrontal cortex of patients with major depressive disorder.重度抑郁症患者死后眶额皮质中环磷酸腺苷反应元件结合蛋白的磷酸化水平降低。
J Neural Transm (Vienna). 2003 Jun;110(6):671-80. doi: 10.1007/s00702-002-0810-8.

抑郁患者中性粒细胞中的环腺苷酸反应元件结合蛋白(CREB)。

Cyclic-AMP response element binding protein (CREB) in the neutrophils of depressed patients.

机构信息

Department of Psychiatry, University of Illinois at Chicago, College of Medicine, Chicago, IL 60612, USA.

出版信息

Psychiatry Res. 2011 Jan 30;185(1-2):108-12. doi: 10.1016/j.psychres.2010.04.013. Epub 2010 May 23.

DOI:10.1016/j.psychres.2010.04.013
PMID:20494459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3000439/
Abstract

Cyclic-AMP response element binding (CREB) protein regulates the expression of many genes involved in the pathophysiology of depression. Increased CREB levels were found in the brain of antidepressant-treated rats and decreased protein and mRNA expression of CREB was reported in the postmortem brain of depressed suicide victims. We determined CREB protein expression, using Western blot technique, and CRE-DNA binding, using gel shift assay, in neutrophils obtained from 22 drug-free patients with major depressive disorder (MDD) and 23 normal control subjects. Diagnosis of patients was based on Diagnostic and Statistical Manual of Mental Disorders DSM-IV criteria; severity of illness was rated by Hamilton Depression Rating Scale (HDRS). We found that the CRE-DNA binding activity and CREB protein expression were significantly decreased in the neutrophils of drug-free MDD patients compared with normal control subjects. Our findings suggest that CREB may play an important role in the pathophysiology of depression and that it may be an important target for the therapeutic action of antidepressant drugs. Neutrophil CREB levels may also serve as a useful biomarker for patients with MDD.

摘要

环磷酸腺苷反应元件结合蛋白(CREB)调节许多参与抑郁症病理生理学的基因的表达。在抗抑郁治疗的大鼠脑中发现 CREB 水平增加,而在抑郁症自杀患者的死后脑中报道 CREB 的蛋白和 mRNA 表达减少。我们使用 Western blot 技术确定了来自 22 名未服用药物的重度抑郁症(MDD)患者和 23 名正常对照者的中性粒细胞中的 CREB 蛋白表达,使用凝胶迁移分析确定了 CRE-DNA 结合。患者的诊断基于精神障碍诊断和统计手册第四版(DSM-IV)标准;疾病严重程度由汉密尔顿抑郁评定量表(HDRS)评定。我们发现,与正常对照组相比,未服用药物的 MDD 患者的中性粒细胞中 CRE-DNA 结合活性和 CREB 蛋白表达显著降低。我们的研究结果表明,CREB 可能在抑郁症的病理生理学中发挥重要作用,并且可能是抗抑郁药物治疗作用的重要靶点。中性粒细胞 CREB 水平也可能是 MDD 患者的有用生物标志物。