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婴儿猝死综合征中延髓弓状核神经元成熟延迟。

Delayed neuronal maturation of the medullary arcuate nucleus in sudden infant death syndrome.

作者信息

Biondo Bruna, Lavezzi AnnaMaria, Tosi Delfina, Turconi Paola, Matturri Luigi

机构信息

Institute of Pathology, University of Milan, Via Commenda 19, 20122 Milan, Italy.

出版信息

Acta Neuropathol. 2003 Dec;106(6):545-51. doi: 10.1007/s00401-003-0757-3. Epub 2003 Sep 12.

Abstract

Recently, quantitative abnormalities in neuronal populations derived from the rhombic lip (inferior olive nucleus of the brain stem and external granular layer of the cerebellum) have been reported in victims of the sudden infant death syndrome (SIDS). In this study we examined the arcuate nucleus (ARCn) of 35 SIDS victims and 25 controls, to determine neuronal abnormalities involving this nucleus in SIDS. Computer-assisted cell evaluation was made on sections stained with hematoxylin and eosin to study the neuronal dimensions (nuclear and cytoplasmic area, nuclear/cytoplasmic ratio), the form factor and the density of reactive astrocytes. There was a significant reduction of the neuronal area (nuclear and cytoplasmic) in SIDS victims compared with controls. The neuronal populations of SIDS victims had a significantly higher form factor, index of immaturity. The SIDS victims were divided into two groups on the basis of ARCn development: 18 SIDS-A cases with a well-developed ARCn and 17 SIDS-B cases with severe bilateral hypoplasia. The results of our research indicate that the developmental defect is characterized by a reduction in size of the ARC neurons and by neuronal depletion. In SIDS the ARCn has the histomorphological features of neuronal immaturity, and there is a marked reduction of all quantitative cell parameters and lower astrocytes density with respect to controls. On the basis of the morphometric results of the arcuate neuronal populations, we hypothesize that infants whose neurons have failed to reach full maturity are at risk for SIDS because they are unable to develop appropriate cardioventilatory control.

摘要

最近,有报道称,婴儿猝死综合征(SIDS)受害者源自菱唇(脑干下橄榄核和小脑外颗粒层)的神经元群体存在数量异常。在本研究中,我们检查了35例SIDS受害者和25例对照者的弓状核(ARCn),以确定SIDS中涉及该核的神经元异常情况。对苏木精和伊红染色的切片进行计算机辅助细胞评估,以研究神经元尺寸(核面积和胞质面积、核/质比)、形态因子和反应性星形胶质细胞密度。与对照组相比,SIDS受害者的神经元面积(核和胞质)显著减小。SIDS受害者的神经元群体具有显著更高的形态因子,即不成熟指数。根据ARCn发育情况,将SIDS受害者分为两组:18例ARCn发育良好的SIDS - A病例和17例双侧严重发育不全的SIDS - B病例。我们的研究结果表明,发育缺陷的特征是ARC神经元尺寸减小和神经元数量减少。在SIDS中,ARCn具有神经元不成熟的组织形态学特征,与对照组相比,所有定量细胞参数均显著降低,星形胶质细胞密度也更低。基于弓状神经元群体的形态测量结果,我们推测神经元未能达到完全成熟的婴儿有患SIDS的风险,因为他们无法发展出适当的心肺通气控制能力。

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