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鸡胚实验性脊柱裂的形态学

Morphology of experimental spina bifida in the chick embryo.

作者信息

Mann R A, Persaud T V

出版信息

Anat Anz. 1979;145(2):182-91.

PMID:382909
Abstract

Open malformations of the central nervous system may involve the brain or spinal cord, or both. Preliminary experiments in which a window was cut in the shell overlying early chick embryos (with removal of 2 ml of albumen) produced a range of neural and non-neural malformations. Exposure of Stage 5--10 embryos at 26 hours of incubation produced open brain and cord defects. Embryos were recovered at 11--12 days for gross examination. Open cord defects in 12 day experimental embryos could be divided morphologically into 2 types. One group showed an everted symmetrical plaque of neural tissue. In the other group the cord defect was more irregular, partly covered by skin, and often combined with rump and trunk defects. Skeletal staining showed that vertebral lesions increased in severity in a cranio-caudal sequence. Spina bifida occulta was found in the cervical and upper thoracic regions; spina bifida manifesta, associated with open cord defects, occurred from the lower thoracic to the sacral regions; vertebral deletions were almost confined to the caudal region. Spina bifida manifesta at the site of open cord defects also showed 2 distinct patterns. Regular cord defects were associated with regular spinal defects, showing loss of spinous processes, reduction of laminae and eversion of the pedicles. Irregular cord defects were associated with more irregular spinal defects showing vertebral deletions or fusions, rumplessness, and pelvic reduction. Neither group, however, showed local kyphosis or scoliosis. Early neurogenesis in the avian and human embryos is very similar with development of the spinal cord from neural plate and tail bud materials which fuse in an overlap zone. These experimental defects in the chick embryo, separable into regular and irregular types thus provide a useful model for investigation of the embryogenesis of spina bifida.

摘要

中枢神经系统的开放性畸形可能累及脑或脊髓,或两者皆有。在早期鸡胚上方的蛋壳上切开一个窗口(去除2毫升蛋白)的初步实验产生了一系列神经和非神经畸形。在孵化26小时时暴露5-10期胚胎会导致开放性脑和脊髓缺陷。在11-12天时回收胚胎进行大体检查。12天实验胚胎中的开放性脊髓缺陷在形态上可分为2种类型。一组显示神经组织外翻对称斑块。另一组脊髓缺陷更不规则,部分被皮肤覆盖,且常合并臀部和躯干缺陷。骨骼染色显示椎骨病变的严重程度从颅侧向尾侧递增。隐性脊柱裂见于颈部和上胸部区域;显性脊柱裂与开放性脊髓缺陷相关,发生于下胸部至骶部区域;椎骨缺失几乎局限于尾侧区域。开放性脊髓缺陷部位的显性脊柱裂也显示出2种不同模式。规则的脊髓缺陷与规则的脊柱缺陷相关,表现为棘突缺失、椎板减少和椎弓根外翻。不规则的脊髓缺陷与更不规则的脊柱缺陷相关,表现为椎骨缺失或融合、无尾畸形和骨盆缩小。然而,两组均未出现局部驼背或脊柱侧弯。鸟类和人类胚胎的早期神经发生非常相似,脊髓由神经板和尾芽材料发育而来,二者在重叠区域融合。鸡胚中的这些实验性缺陷可分为规则型和不规则型,因此为脊柱裂的胚胎发生研究提供了一个有用的模型。

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