Bruni J E, del Bigio M R, Cardoso E R, Persaud T V
Department of Anatomy, University of Manitoba, Winnipeg, Canada.
Acta Neurochir (Wien). 1988;92(1-4):118-22. doi: 10.1007/BF01401981.
The neuropathology of congenital hydrocephalus in SUMS/NP mice was investigated in this study. Hydrocephalus occurred with an incidence of 16.5% and was evident in the form of an enlarged head soon after birth. The condition was progressive; affected mice gradually became noticeably smaller than normals, acquired functional disturbances and died before ever breeding. Hydrocephalic mice exhibited enormous dilatation of the lateral ventricles, thinning of the cortex and compression and distortion of the diencephalon and striatum. Examination of the midbrain in these animals revealed that the proximal cerebral aqueduct was diminished in size, occluded or absent. Evidence of its anomalous development was seen as early as day 15 of foetal development. This is in substantial agreement with previous reports on this strain. Although the mechanism by which this occurs is still unknown, abnormal development of the adjoining diencephalon and/or rostral midbrain is likely to be involved.
本研究对SUMS/NP小鼠先天性脑积水的神经病理学进行了调查。脑积水的发生率为16.5%,出生后不久即表现为头部增大。病情呈进行性发展;受影响的小鼠逐渐明显小于正常小鼠,出现功能障碍,并在繁殖前死亡。脑积水小鼠表现出侧脑室极度扩张、皮质变薄以及间脑和纹状体受压和变形。对这些动物中脑的检查发现,大脑导水管近端尺寸减小、闭塞或缺失。早在胎儿发育的第15天就可见到其异常发育的迹象。这与此前关于该品系的报道基本一致。尽管其发生机制尚不清楚,但相邻间脑和/或中脑前部的异常发育可能与之有关。