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用于探究精神分裂症患者死后大脑扣带回皮质神经回路的模型生成与测试

Model generation and testing to probe neural circuitry in the cingulate cortex of postmortem schizophrenic brain.

作者信息

Benes F M

机构信息

Laboratory for Structural Neuroscience, McLean Hospital, Belmont, MA 02178, USA.

出版信息

Schizophr Bull. 1998;24(2):219-30. doi: 10.1093/oxfordjournals.schbul.a033322.

Abstract

In the past decade, there has been increased interest in whether discreet alterations of neural circuitry might play a role in the pathophysiology of schizophrenia. In the absence of a readily identifiable histopathology, a variety of sophisticated neurobiological approaches is being applied to the study of this disorder. In one series of investigations, subtle abnormalities have been detected in the anterior cingulate cortex-layer II (ACCx-II) of schizophrenia patients. One of these studies suggested a reduction of nonpyramidal neurons in schizophrenia patients, and it was postulated that this change could give rise to a relative increase of dopaminergic inputs to the remaining gamma-aminobutyric acid (GABA) cells. Although empiric evidence in support of this hypothesis was obtained, a subsequent post hoc analysis, described in this report, has suggested that this change could have occurred irrespective of whether GABA cells are reduced in number. A shift of cortical dopamine afferents from pyramidal to nonpyramidal neurons in ACCx-II seems to provide a more plausible explanation for such a "miswiring." These findings support critical use of model generation and testing as powerful tools for unraveling the nature of altered neural circuitry in postmortem schizophrenic brain.

摘要

在过去十年中,人们越来越关注神经回路的细微改变是否可能在精神分裂症的病理生理学中发挥作用。由于缺乏易于识别的组织病理学特征,各种复杂的神经生物学方法正被应用于该疾病的研究。在一系列调查中,已在精神分裂症患者的前扣带回皮质第二层(ACCx-II)中检测到细微异常。其中一项研究表明精神分裂症患者的非锥体神经元减少,据推测这种变化可能导致多巴胺能输入到剩余的γ-氨基丁酸(GABA)细胞的相对增加。尽管获得了支持这一假设的经验证据,但本报告中描述的后续事后分析表明,无论GABA细胞数量是否减少,这种变化都可能发生。ACCx-II中皮质多巴胺传入从锥体神经元向非锥体神经元的转移似乎为这种“线路错误”提供了更合理的解释。这些发现支持将模型生成和测试作为揭示死后精神分裂症大脑中神经回路改变本质的有力工具进行批判性使用。

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