Suppr超能文献

沙利度胺与神经营养作用

Thalidomide and neurotrophism.

作者信息

Soper Judith R, Bonar S Fiona, O'Sullivan Dudley J, McCredie Janet, Willert Hans-Georg

机构信息

Diagnostic Radiology, Royal Prince Alfred Hospital, Missenden Rd, Camperdown, Sydney, NSW, Australia.

Specialist Magnetic Resonance Imaging Carillon Ave Newtown, Sydney, NSW, Australia.

出版信息

Skeletal Radiol. 2019 Apr;48(4):517-525. doi: 10.1007/s00256-018-3086-2. Epub 2018 Oct 19.

Abstract

BACKGROUND

Following the thalidomide disaster (1958-62), Henkel and Willert analysed the pattern of dysmelia in the long bones (J Bone Joint Surg Br. 51:399-414, 1969) and the extremities, Willert and Henkel (Z Orthop Ihre Grenzgeb. 107:663-75, 1970). Willert's material from deformed extremities is re-examined here asking "How does thalidomide reduce the skeleton?"

MATERIALS AND METHODS

We reviewed the original data collection of Willert and Henkel (Z Orthop Ihre Grenzgeb. 107:663-75, 1970), comprising musculoskeletal histology slides from 30 children affected by thalidomide with radiographs of hands (19 cases) and feet (4 cases).

RESULTS

All original observations by Willert and Henkel (Z Orthop Ihre Grenzgeb. 107:663-75, 1970), were verified. Radial rays of the hand disappeared early, but the foot was spared until late. Radiology confirms that bone reduction in the hand (aplasia or hypoplasia in the thumb and index finger) coincides with sensory segmental nerve C6. In the foot, reduction of the toes is rare, but mesenchymal excess (polydactyly) occurs in the hallux (L5 sclerotome), usually associated with absent tibia (L4 sclerotome). Histology confirms skeletal mesenchymal components to be unremarkable, contrasting with grossly abnormal bony architecture, a striking discordance between microscopic and macroscopic findings. No necrosis or vascular pathology was seen.

CONCLUSION

The basic lesion was an abnormal quantity rather than quality of mesenchyme. Cell populations result from cellular proliferation, controlled in early limb bud formation by neurotrophism. Thalidomide is a known sensory neurotoxin in adults. In the embryo, sensorineural injury alters neurotrophism, causing increased or diminished cell proliferation in undifferentiated mesenchyme. Differentiation into normal cartilage occurs later, but within an altered mesenchymal mass. Reduction or excess deformity results, with normal histology, a significant finding. The primary pathological condition is not in the skeleton, but in the nerves.

摘要

背景

在沙利度胺灾难(1958 - 1962年)之后,亨克尔和维勒特分析了长骨(《英国骨与关节外科杂志》。51:399 - 414,1969年)和四肢的肢体短缩模式,维勒特和亨克尔(《矫形外科学及其相关领域》。107:663 - 75,1970年)。此处重新审视了维勒特取自畸形肢体的材料,提出问题“沙利度胺如何影响骨骼?”

材料与方法

我们回顾了维勒特和亨克尔(《矫形外科学及其相关领域》。107:663 - 75,1970年)的原始数据收集,包括30例受沙利度胺影响儿童的肌肉骨骼组织学切片以及手部(19例)和足部(4例)的X线片。

结果

维勒特和亨克尔(《矫形外科学及其相关领域》。107:663 - 75,1970年)的所有原始观察结果均得到验证。手部桡侧射线早期消失,但足部直到后期才受影响。放射学证实手部骨骼减少(拇指和示指发育不全或发育不良)与感觉节段神经C6相对应。在足部,脚趾减少很少见,但踇趾(L5节段)出现间充质过剩(多指畸形),通常伴有胫骨缺失(L4节段)。组织学证实骨骼间充质成分无明显异常,与严重异常的骨骼结构形成对比,微观和宏观发现之间存在显著差异。未观察到坏死或血管病变。

结论

基本病变是间充质数量异常而非质量异常。细胞群体源于细胞增殖,在肢体芽早期形成过程中受神经营养作用控制。沙利度胺在成人中是一种已知的感觉神经毒素。在胚胎中,感觉神经损伤会改变神经营养作用,导致未分化间充质中细胞增殖增加或减少。随后分化为正常软骨,但在改变的间充质团块内进行。导致减少或过度畸形,组织学正常,这是一个重要发现。主要病理状况不在骨骼,而在神经。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6409/6394469/436c5afe10c7/256_2018_3086_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验