• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

精神分裂症、双相情感障碍和单相重度抑郁症患者背外侧前额叶皮质深层白质的髓鞘染色

Myelin staining of deep white matter in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and unipolar major depression.

作者信息

Regenold William T, Phatak Pornima, Marano Christopher M, Gearhart Lorie, Viens Claudia H, Hisley K Calvin

机构信息

University of Maryland School of Medicine, Department of Psychiatry, Division of Geriatric Psychiatry and the Baltimore Veterans Affairs Medical Center, Baltimore, MD 21201, USA.

出版信息

Psychiatry Res. 2007 Jun 30;151(3):179-88. doi: 10.1016/j.psychres.2006.12.019. Epub 2007 Apr 11.

DOI:10.1016/j.psychres.2006.12.019
PMID:17433451
Abstract

Neuroimaging and postmortem studies suggest the involvement of white matter disease in schizophrenia, bipolar disorder, and unipolar major depression. To date there is no published, collective study of myelin staining in these three psychiatric disorders. Deep white matter lesions, potentially affecting corticolimbic circuits, have been particularly implicated in late life depression and poor outcome bipolar disorder. We hypothesized that individuals with these disorders would manifest reduced deep white matter myelin staining compared to normal controls. Sixty transverse sections of fixed dorsolateral prefrontal cortex - 15 from individuals with each psychiatric disorder and 15 from normal controls - were stained according to the method of Kluver and Barrera. Myelin staining intensity was quantified by digital image analysis and expressed as a percent of grey matter staining for a given section. Mean deep (but not gyral) white matter myelin staining was less intense in all three psychiatric groups compared to control. This difference was statistically significant for the bipolar and unipolar groups, with a strong trend toward attenuated staining in the schizophrenic group. Our findings are consistent with postmortem and neuroimaging studies of affective disorders that indicate an increased prevalence of deep white matter lesions in unipolar and bipolar affective disorders.

摘要

神经影像学和尸检研究表明,白质疾病与精神分裂症、双相情感障碍和单相重度抑郁症有关。迄今为止,尚未有关于这三种精神疾病髓鞘染色的公开的集体研究。深部白质病变可能影响皮质边缘回路,尤其与老年抑郁症和双相情感障碍的不良预后有关。我们假设,与正常对照组相比,患有这些疾病的个体深部白质髓鞘染色会减少。根据Kluver和Barrera的方法,对60个固定的背外侧前额叶皮质横切片进行染色,其中15个来自每种精神疾病患者,15个来自正常对照组。通过数字图像分析对髓鞘染色强度进行量化,并表示为给定切片灰质染色的百分比。与对照组相比,所有三个精神疾病组的平均深部(而非脑回)白质髓鞘染色强度均较低。双相情感障碍组和单相情感障碍组的这种差异具有统计学意义,精神分裂症组有染色减弱的强烈趋势。我们的研究结果与情感障碍的尸检和神经影像学研究一致,并表明单相和双相情感障碍中深部白质病变的患病率增加。

相似文献

1
Myelin staining of deep white matter in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and unipolar major depression.精神分裂症、双相情感障碍和单相重度抑郁症患者背外侧前额叶皮质深层白质的髓鞘染色
Psychiatry Res. 2007 Jun 30;151(3):179-88. doi: 10.1016/j.psychres.2006.12.019. Epub 2007 Apr 11.
2
Altered intracortical myelin staining in the dorsolateral prefrontal cortex in severe mental illness.严重精神疾病患者背外侧前额叶皮质内皮质髓鞘染色改变。
Eur Arch Psychiatry Clin Neurosci. 2017 Aug;267(5):369-376. doi: 10.1007/s00406-016-0730-5. Epub 2016 Sep 14.
3
Mitochondrial complex I subunits expression is altered in schizophrenia: a postmortem study.精神分裂症中线粒体复合物I亚基表达发生改变:一项尸检研究
Biol Psychiatry. 2004 Apr 1;55(7):676-84. doi: 10.1016/j.biopsych.2003.12.012.
4
Localization of white-matter lesions and effect of vascular risk factors in late-onset major depression.脑白质病变的定位及其与血管危险因素在迟发性重度抑郁症中的作用。
Psychol Med. 2010 Aug;40(8):1389-99. doi: 10.1017/S0033291709991656. Epub 2009 Nov 9.
5
Genetic risk for white matter abnormalities in bipolar disorder.双相障碍患者脑白质异常的遗传风险。
Int Rev Psychiatry. 2009;21(4):387-93. doi: 10.1080/09540260902962180.
6
Application of a multifractal analysis to study brain white matter abnormalities of schizophrenia on T2-weighted magnetic resonance imaging.应用多重分形分析研究精神分裂症患者T2加权磁共振成像上的脑白质异常。
Psychiatry Res. 2009 Mar 31;171(3):177-88. doi: 10.1016/j.pscychresns.2008.03.009. Epub 2009 Feb 12.
7
Density and distribution of white matter neurons in schizophrenia, bipolar disorder and major depressive disorder: no evidence for abnormalities of neuronal migration.精神分裂症、双相情感障碍和重度抑郁症中白质神经元的密度和分布:无神经元迁移异常的证据。
Mol Psychiatry. 2002;7(6):564-70. doi: 10.1038/sj.mp.4001038.
8
Biophysical changes in normal-appearing white matter and subcortical nuclei in late-life major depression detected using magnetization transfer.使用磁化传递检测晚年重度抑郁症患者正常外观白质和皮质下核的生物物理变化。
Psychiatry Res. 2004 Feb 15;130(2):131-40. doi: 10.1016/j.pscychresns.2003.12.002.
9
Elevation of cell adhesion molecule immunoreactivity in the anterior cingulate cortex in bipolar disorder.双相情感障碍患者前扣带回皮质中细胞黏附分子免疫反应性升高。
Biol Psychiatry. 2004 Mar 15;55(6):652-5. doi: 10.1016/j.biopsych.2003.10.015.
10
Upregulation of the initiating step of the kynurenine pathway in postmortem anterior cingulate cortex from individuals with schizophrenia and bipolar disorder.精神分裂症和双相情感障碍患者死后前扣带回皮质中犬尿氨酸途径起始步骤的上调。
Brain Res. 2006 Feb 16;1073-1074:25-37. doi: 10.1016/j.brainres.2005.12.056. Epub 2006 Jan 30.

引用本文的文献

1
The role of low subcortical iron, white matter myelin, and oligodendrocytes in schizophrenia: a quantitative susceptibility mapping and diffusion tensor imaging study.皮层下低铁、白质髓鞘和少突胶质细胞在精神分裂症中的作用:一项定量磁化率成像和扩散张量成像研究
Mol Psychiatry. 2025 Sep 5. doi: 10.1038/s41380-025-03195-7.
2
Ferroptosis as a potential molecular mechanism of bipolar disorder.铁死亡作为双相情感障碍的一种潜在分子机制。
Transl Psychiatry. 2025 Jun 19;15(1):205. doi: 10.1038/s41398-025-03429-w.
3
Myelin dysfunction in aging and brain disorders: mechanisms and therapeutic opportunities.
衰老与脑部疾病中的髓鞘功能障碍:机制与治疗机遇
Mol Neurodegener. 2025 Jun 15;20(1):69. doi: 10.1186/s13024-025-00861-w.
4
Myelin Repair as a Novel Mechanism for Ketamine's Sustained Antidepressant Effects.髓鞘修复作为氯胺酮持续抗抑郁作用的一种新机制。
Curr Neuropharmacol. 2025;23(8):943-955. doi: 10.2174/011570159X349856241213144902.
5
Glial cell deficits are a key feature of schizophrenia: implications for neuronal circuit maintenance and histological differentiation from classical neurodegeneration.神经胶质细胞缺陷是精神分裂症的一个关键特征:对神经元回路维持及与经典神经退行性变在组织学上的区分的影响。
Mol Psychiatry. 2025 Mar;30(3):1102-1116. doi: 10.1038/s41380-024-02861-6. Epub 2024 Dec 5.
6
Oligodendroglial fatty acid metabolism as a central nervous system energy reserve.少突胶质细胞脂肪酸代谢作为中枢神经系统的能量储备。
Nat Neurosci. 2024 Oct;27(10):1934-1944. doi: 10.1038/s41593-024-01749-6. Epub 2024 Sep 9.
7
Leveraging ultra-high field (7T) MRI in psychiatric research.利用超高场(7T)磁共振成像在精神医学研究中的应用。
Neuropsychopharmacology. 2024 Nov;50(1):85-102. doi: 10.1038/s41386-024-01980-6. Epub 2024 Sep 9.
8
Brain structure, amyloid, and behavioral features for predicting clinical progression in subjective cognitive decline.用于预测主观认知下降临床进展的脑结构、淀粉样蛋白和行为特征。
Hum Brain Mapp. 2024 Jul 15;45(10):e26765. doi: 10.1002/hbm.26765.
9
The effects of venlafaxine on depressive-like behaviors and gut microbiome in cuprizone-treated mice.文拉法辛对用铜螯合剂处理的小鼠的抑郁样行为和肠道微生物群的影响。
Front Psychiatry. 2024 Jun 3;15:1347867. doi: 10.3389/fpsyt.2024.1347867. eCollection 2024.
10
FOXO1 reshapes neutrophils to aggravate acute brain damage and promote late depression after traumatic brain injury.FOXO1 重塑中性粒细胞,加重创伤性脑损伤后的急性脑损伤,并促进迟发性抑郁。
Mil Med Res. 2024 Mar 31;11(1):20. doi: 10.1186/s40779-024-00523-w.