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前额叶皮质中神经元和神经胶质体细胞体大小:精神分裂症和亨廷顿病的尸检形态计量学研究

Neuronal and glial somal size in the prefrontal cortex: a postmortem morphometric study of schizophrenia and Huntington disease.

作者信息

Rajkowska G, Selemon L D, Goldman-Rakic P S

机构信息

Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson 39216, USA.

出版信息

Arch Gen Psychiatry. 1998 Mar;55(3):215-24. doi: 10.1001/archpsyc.55.3.215.

Abstract

BACKGROUND

The cortex of patients with schizophrenia exhibits a deficit in neuropil, but the nature and extent of cellular abnormalities remain unclear. To gain further insight into this abnormality, neuronal and glial somal size were analyzed in postmortem brains from 9 patients with schizophrenia, 10 normal (control) patients, and 7 patients with Huntington disease, the latter representing a known neurodegenerative disorder.

METHODS

A 3-dimensional image analyzer was used to measure the perimeters of 10722 neuronal and 19913 glial profiles in Brodmann areas 9 and 17. Neurons and glia were classified by size and layer to assess specific vulnerabilities with respect to cortical architecture and circuitry.

RESULTS

The schizophrenic prefrontal cortex was characterized by a downward shift in neuronal sizes accompanied by 70% to 140% per layer increases in the density of small neurons. In layer III only, a significant reduction in mean neuronal size was associated with a significant decrease in the density of very large neurons in sublayer Illc. Neither neuronal size in occipital area 17 nor glial size in prefrontal or occipital cortexes were reduced. In cortex with Huntington disease, neuronal degeneration was evidenced by concurrence of reduced neuronal size, decreased density of large neurons, and dramatic elevation in density of large glia.

CONCLUSIONS

Distinct cytometric abnormalities support the hypothesis that neuronal degeneration in the prefrontal cortex is not a prominent feature of the neuropathological changes in schizophrenia, although an ongoing process in Huntington disease. Rather, schizophrenia appears to involve more subtle abnormalities, with the largest corticocortical projection neurons of layer IIIc expressing the greatest somal reduction.

摘要

背景

精神分裂症患者的皮质表现出神经毡缺陷,但细胞异常的性质和程度仍不清楚。为了进一步了解这种异常,对9例精神分裂症患者、10例正常(对照)患者和7例亨廷顿病患者的尸检大脑中的神经元和神经胶质体细胞体大小进行了分析,后者代表一种已知的神经退行性疾病。

方法

使用三维图像分析仪测量布罗德曼9区和17区中10722个神经元和19913个神经胶质细胞轮廓的周长。根据大小和层对神经元和神经胶质细胞进行分类,以评估相对于皮质结构和回路的特定易损性。

结果

精神分裂症患者的前额叶皮质的特征是神经元大小向下偏移,同时每层小神经元密度增加70%至140%。仅在Ⅲ层,平均神经元大小的显著减小与Ⅲc亚层中非常大的神经元密度的显著降低相关。枕叶17区的神经元大小以及前额叶或枕叶皮质中的神经胶质细胞大小均未减小。在患有亨廷顿病的皮质中,神经元大小减小、大神经元密度降低和大神经胶质细胞密度显著升高同时出现,证明存在神经元变性。

结论

明显的细胞计数异常支持这样的假设,即前额叶皮质中的神经元变性不是精神分裂症神经病理变化的突出特征,尽管在亨廷顿病中是一个持续的过程。相反,精神分裂症似乎涉及更细微的异常,Ⅲc层中最大的皮质-皮质投射神经元表现出最大程度的细胞体缩小。

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