Rioux Lise, Nissanov Jonathan, Lauber Katherine, Bilker Warren B, Arnold Steven E
Department of Psychiatry, University of Pennsylvania, 547 Clinical Research Bldg., 415 Curie Blvd., Philadelphia, PA 19104-6140, USA.
Am J Psychiatry. 2003 Jan;160(1):149-55. doi: 10.1176/appi.ajp.160.1.149.
Evidence suggests that schizophrenia is a neurodevelopmental disorder that may involve abnormal connectivity between various cortical and subcortical brain areas. The parahippocampal gyrus is an area important for higher cognition in which a variety of cytoarchitectural, neuronal morphometric, and innervation abnormalities in schizophrenia have been reported. Previous studies have reported abnormal distributions of interstitial white matter neurons in prefrontal, parietal, and temporal neocortices, which suggests that schizophrenia may be related to prenatal disturbances in the cortical subplate, a transitory structure involved in the formation of connections in the developing cortex from which the interstitial white matter neurons derive. Abnormalities in the distribution of interstitial white matter neurons in the parahippocampal gyrus in schizophrenia may indicate an alteration in the migration of subplate neurons or in the pattern of programmed cell death that could lead to defective cortical circuitry and impaired cognition.
The authors used a monoclonal antibody against the microtubule-associated protein MAP2 to label interstitial white matter neurons in the anterior region of the parahippocampal gyrus from 41 individuals with schizophrenia and 15 comparison subjects. The distribution of MAP2-labeled neurons in relation to the gray matter/white matter boundary was determined by computer-assisted microscopy.
The number of interstitial white matter neurons decreased with increasing white matter depth in both groups, but significantly more slowly in the schizophrenia group, with interstitial white matter neurons located deeper in white matter in schizophrenia subjects.
These findings indicate there is an abnormality in the residua of the cortical subplate in the anterior region of the adult parahippocampal gyrus in schizophrenia subjects.
有证据表明精神分裂症是一种神经发育障碍,可能涉及大脑各皮质和皮质下区域之间的异常连接。海马旁回是对高级认知很重要的一个区域,已有报道称精神分裂症患者在此区域存在多种细胞结构、神经元形态测量和神经支配异常。先前的研究报道了前额叶、顶叶和颞叶新皮质中间质白质神经元的异常分布,这表明精神分裂症可能与皮质下板的产前紊乱有关,皮质下板是一个过渡结构,参与发育中皮质连接的形成,而间质白质神经元即源自于此。精神分裂症患者海马旁回中间质白质神经元分布异常可能表明皮质下板神经元迁移或程序性细胞死亡模式发生改变,这可能导致皮质回路缺陷和认知受损。
作者使用一种针对微管相关蛋白MAP2的单克隆抗体,对41例精神分裂症患者和15名对照受试者海马旁回前部区域的间质白质神经元进行标记。通过计算机辅助显微镜确定MAP2标记神经元相对于灰质/白质边界的分布。
两组中间质白质神经元的数量均随白质深度增加而减少,但精神分裂症组减少得明显更慢,精神分裂症患者的间质白质神经元位于白质更深的位置。
这些发现表明,精神分裂症患者成年海马旁回前部区域的皮质下板残余存在异常。