Jacobsson C, Granström G
Department of Pedodontics, University of Gothenburg, Sweden.
ORL J Otorhinolaryngol Relat Spec. 1997 May-Jun;59(3):147-54. doi: 10.1159/000276928.
Malformations of the cranial base, temporal bone and middle ear were induced in the offspring of Sprague-Dawley rats by a single intraperitoneal injection of 10-30 mg/kg etretinate (Tigasone) at days 8.5-10.5 of gestation. By differential staining of the embryonic craniofacial cartilage and bone, and microdissection of the otomandibular complex, the induced malformations were studied specifically. Defective formations of Meckel's cartilage and the cartilaginous skull base were found to be prominent features of the malformation. The malformation included defective middle-ear ossicles; especially the malleus and incus were fused with a shorter than normal long process and manubrium. In conjunction with the distal part of Meckel's cartilage, mandibular micrognathia was observed. All of the malformed tissues are derivatives of the first and second branchial arches. The teratogenically induced defects in the rat embryos show some similarities to the clinical syndromes of the first and second branchial arches in man.
在妊娠第8.5至10.5天,通过腹腔内单次注射10 - 30 mg/kg依曲替酯(银屑灵),诱导斯普拉格-道利大鼠后代出现颅底、颞骨和中耳畸形。通过对胚胎颅面软骨和骨骼进行差异染色,以及对耳下颌复合体进行显微解剖,专门研究了诱导产生的畸形。发现梅克尔软骨和软骨性颅底的形成缺陷是畸形的突出特征。畸形包括中耳听小骨缺陷;特别是锤骨和砧骨融合,其长突和柄部比正常短。与梅克尔软骨的远端部分相连,观察到下颌小颌畸形。所有畸形组织均为第一和第二鳃弓的衍生物。大鼠胚胎中致畸剂诱导的缺陷与人第一和第二鳃弓的临床综合征有一些相似之处。