Mood disorders are glial disorders: evidence from in vivo studies.

Cardiovascular psychiatry and neurology Pub Date : 2010-01-01 Epub Date: 2010-05-27 DOI:10.1155/2010/780645
Matthias L Schroeter, Hashim Abdul-Khaliq, Julia Sacher, Johann Steiner, Ingolf E Blasig, Karsten Mueller
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引用次数: 70

Abstract

It has recently been suggested that mood disorders can be characterized by glial pathology as indicated by histopathological postmortem findings. Here, we review studies investigating the glial marker S100B in serum of patients with mood disorders. This protein might act as a growth and differentiation factor. It is located in, and may actively be released by, astro- and oligodendrocytes. Studies consistently show that S100B is elevated in mood disorders; more strongly in major depressive than bipolar disorder. Successful antidepressive treatment reduces S100B in major depression whereas there is no evidence of treatment effects in mania. In contrast to the glial marker S100B, the neuronal marker protein neuron-specific enolase is unaltered. By indicating glial alterations without neuronal changes, serum S100B studies confirm specific glial pathology in mood disorders in vivo. S100B can be regarded as a potential diagnostic biomarker for mood disorders and as a biomarker for successful antidepressive treatment.

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情绪障碍是神经胶质障碍:来自体内研究的证据。
最近有研究表明,死后组织病理学结果表明,情绪障碍可以通过神经胶质病理来表征。在此,我们回顾了有关情绪障碍患者血清中神经胶质标志物S100B的研究。这种蛋白可能是一种生长和分化因子。它位于星形胶质细胞和少突胶质细胞中,并可能被其积极释放。研究一致表明,S100B在情绪障碍中升高;重度抑郁症比双相情感障碍更强烈。成功的抗抑郁治疗可降低重度抑郁症患者的S100B,而没有证据表明治疗对躁狂症有效果。与胶质标记物S100B相反,神经元标记蛋白神经元特异性烯醇化酶没有改变。血清S100B研究通过表明神经胶质的改变而没有神经元的改变,证实了体内情绪障碍中特定的神经胶质病理。S100B可被视为情绪障碍的潜在诊断生物标志物和成功抗抑郁治疗的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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