Burk D T, Willhite C C
Department of Anatomy, University of the Pacific School of Dentistry, San Francisco, California 94115.
Teratology. 1992 Aug;46(2):147-57. doi: 10.1002/tera.1420460208.
Inner ear malformations induced in anotic hamster fetuses following maternal treatment with 50 mg/kg isotretinoin (13-cis-retinoic acid) on gestational day 8 are described. Computer-assisted three dimensional reconstruction was used. Two general types of defective vestibulocochlear development were seen. Defects were bilateral and correlated with extent of middle ear deficiency and severity of mandibular defects. In the more severely affected fetuses the inner ear was limited to an epithelial sac with occasional small projections, no apparent innervation and a correspondingly reduced otic capsule. In most of the fetuses examined the inner ear was less severely affected and was characterized by a reduction in the number of semicircular ducts and alterations in the size and shape of the cochlear duct. These defects are similar to those seen in a child with the isotretinoin embryopathy. Pathogenesis may result from a direct effect on otic epithelium or from faulty inductive interactions with the rhombencephalon or with periotic neural crest cells.
描述了在妊娠第8天母体用50mg/kg异维甲酸(13 - 顺式维甲酸)处理后,无耳仓鼠胎儿诱导产生的内耳畸形。采用了计算机辅助三维重建。观察到两种一般类型的前庭蜗发育缺陷。缺陷是双侧的,并且与中耳缺陷的程度和下颌缺陷的严重程度相关。在受影响更严重的胎儿中,内耳仅限于一个上皮囊,偶尔有小突起,无明显神经支配,耳囊相应缩小。在大多数检查的胎儿中,内耳受影响较轻,其特征是半规管数量减少以及耳蜗管大小和形状改变。这些缺陷与异维甲酸胚胎病患儿中所见的缺陷相似。发病机制可能是由于对内耳上皮的直接作用,或者是与菱脑或耳周神经嵴细胞的诱导相互作用异常所致。