Suppr超能文献

精神分裂症和双相情感障碍中的扣带回白质神经元

Cingulate white matter neurons in schizophrenia and bipolar disorder.

作者信息

Connor Caroline M, Guo Yin, Akbarian Schahram

机构信息

Program in Neurobiology, Graduate School of Biomedical Sciences, Department of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts 01604, USA.

出版信息

Biol Psychiatry. 2009 Sep 1;66(5):486-93. doi: 10.1016/j.biopsych.2009.04.032. Epub 2009 Jun 25.

Abstract

BACKGROUND

Increased neuronal density in prefrontal, parietal, and temporal white matter of schizophrenia subjects is thought to reflect disordered neurodevelopment; however, it is not known if this cellular alteration affects the cingulate cortex and whether similar changes exist in bipolar disorder.

METHOD

Eighty-two postmortem specimens (bipolar 15, schizophrenia 22, control 45) were included in this clinical study. Densities for two neuronal markers, neuron-specific nuclear protein (NeuN) and neuregulin 1 alpha (NRG), were determined in white matter up to 2.5 mm beneath the anterior cingulate cortex; density of NeuN immunopositive neurons (NeuN+) was also determined for a subset of cases in prefrontal cortex. Changes during normal development were monitored in a separate cohort of 14 brains.

RESULTS

Both the schizophrenia and bipolar cohorts demonstrated a twofold increase in NeuN+ density in cingulate white matter; this effect could be attributed to approximately 25% of cases that exceeded the second standard deviation from control subjects. Similar changes were observed in prefrontal cortex. In contrast density of NRG expressing neurons was unaltered. Cases with increased NeuN+ densities in two-dimensional (2-D) counts also showed a pronounced, > fivefold elevation in NeuN+ nuclei per cubic millimeter. Additionally, the developmental cohort demonstrated a 75% decline in NeuN+ neuronal density during the first postnatal year but was stable thereafter.

CONCLUSIONS

Increased neuronal density in white matter of cingulate cortex in schizophrenia provides further evidence that this alteration occurs in multiple cortical areas. Similar changes in some cases with bipolar illness suggest that the two disorders may share a common underlying defect in late prenatal or early postnatal neurodevelopment.

摘要

背景

精神分裂症患者前额叶、顶叶和颞叶白质中神经元密度增加被认为反映了神经发育紊乱;然而,尚不清楚这种细胞改变是否会影响扣带回皮质,以及双相情感障碍是否存在类似变化。

方法

本临床研究纳入了82个尸检标本(双相情感障碍15例、精神分裂症22例、对照45例)。在前扣带回皮质下方2.5毫米以内的白质中测定两种神经元标志物神经元特异性核蛋白(NeuN)和神经调节蛋白1α(NRG)的密度;还对前额叶皮质部分病例的NeuN免疫阳性神经元(NeuN+)密度进行了测定。在另一组14个大脑中监测正常发育过程中的变化。

结果

精神分裂症和双相情感障碍队列的扣带回白质中NeuN+密度均增加了两倍;这种效应可归因于约25%的病例,其超出了对照组第二个标准差。在前额叶皮质也观察到了类似变化。相比之下,表达NRG的神经元密度未改变。二维计数中NeuN+密度增加的病例每立方毫米NeuN+细胞核也有明显的、超过五倍的升高。此外,发育队列显示出生后第一年NeuN+神经元密度下降了75%,但此后保持稳定。

结论

精神分裂症患者扣带回皮质白质中神经元密度增加进一步证明这种改变发生在多个皮质区域。双相情感障碍部分病例的类似变化表明,这两种疾病可能在产前晚期或产后早期神经发育中存在共同的潜在缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cc/2725195/4626a9011387/nihms128864f1.jpg

相似文献

1
Cingulate white matter neurons in schizophrenia and bipolar disorder.精神分裂症和双相情感障碍中的扣带回白质神经元
Biol Psychiatry. 2009 Sep 1;66(5):486-93. doi: 10.1016/j.biopsych.2009.04.032. Epub 2009 Jun 25.

引用本文的文献

1
Imaging of the superficial white matter in health and disease.健康与疾病状态下的脑白质浅层影像学表现
Imaging Neurosci (Camb). 2024 Jul 22;2. doi: 10.1162/imag_a_00221. eCollection 2024.

本文引用的文献

2
Neurogenesis in the chronic lesions of multiple sclerosis.多发性硬化症慢性病灶中的神经发生
Brain. 2008 Sep;131(Pt 9):2366-75. doi: 10.1093/brain/awn157. Epub 2008 Jul 23.
3
Velo-cardio-facial syndrome: 30 Years of study.腭心面综合征:30年研究历程
Dev Disabil Res Rev. 2008;14(1):3-10. doi: 10.1002/ddrr.2.
5
Neurodevelopmental basis of bipolar disorder: a critical appraisal.双相情感障碍的神经发育基础:批判性评估
Prog Neuropsychopharmacol Biol Psychiatry. 2008 Oct 1;32(7):1617-27. doi: 10.1016/j.pnpbp.2008.04.017. Epub 2008 May 7.
7
Properties of persistent postnatal cortical subplate neurons.出生后持续性皮质下板神经元的特性
J Neurosci. 2007 Sep 12;27(37):9962-74. doi: 10.1523/JNEUROSCI.1536-07.2007.

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