Conrad A J, Scheibel A B
Dept. of Anatomy, UCLA Medical Center 90024.
Schizophr Bull. 1987;13(4):577-87. doi: 10.1093/schbul/13.4.577.
Recent studies suggest that consistent structural changes exist in the hippocampi of schizophrenic patients. These alterations are characterized by a significant degree of disorientation of the hippocampal pyramidal cells when compared with age-matched nonschizophrenic controls. The degree of neuronal disorientation seems to correlate positively with the severity of the clinical picture. A hypothesis on the pathogenesis of this process, suggested in an earlier article, is extended here. Putative maternal infection with one of several neuraminidase-bearing viruses, especially during the second trimester of pregnancy, may severely affect the migration of primitive neurons into the primordial hippocampus. The "neuraminidase effect," expressed through alteration of the normal sequential patterns of N-CAM (neuronal-cell adhesion molecule) maturation, may result in the cellular disarray we have noted. This alteration may prove useful as a cell marker for schizophrenia, even though its actual relation to clinical symptomatology has still to be evaluated. Genetic factors also are believed to be involved, perhaps in the form of certain patterns of reduced immunocompetence, which might render the mother more susceptible to viral infection.
最近的研究表明,精神分裂症患者的海马体存在持续的结构变化。与年龄匹配的非精神分裂症对照相比,这些改变的特征是海马锥体细胞明显定向障碍。神经元定向障碍的程度似乎与临床症状的严重程度呈正相关。本文扩展了早期一篇文章中提出的关于这一过程发病机制的假说。推测母亲感染了几种携带神经氨酸酶的病毒之一,尤其是在妊娠中期,可能会严重影响原始神经元向原始海马体的迁移。通过改变N-CAM(神经细胞粘附分子)成熟的正常顺序模式所表现出的“神经氨酸酶效应”,可能导致我们所观察到的细胞紊乱。这种改变可能被证明是精神分裂症的一种细胞标志物,尽管其与临床症状学的实际关系仍有待评估。遗传因素也被认为与之有关,可能是以某些免疫能力降低模式的形式,这可能使母亲更容易受到病毒感染。