人类大脑的发育。

Bibliotheca anatomica Pub Date : 1986-01-01
H J Kretschmann, G Kammradt, I Krauthausen, B Sauer, F Wingert
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引用次数: 0

摘要

从Yakovlev Collection中选择了25个符合规范性标准的男性大脑,并在适合形态计量学研究的系列切片中可用。根据广义logistic函数计算生长参数。理想体重为1313 g (SD = 41),半值时间为387 (SD = 26)个体发生日,生长因子为4.0 (SD = 0.5)。对汉诺威医学院神经解剖系收集的161个正常男性大脑样本的生长参数进行比较,发现理想体重为1353 g (SD = 14),半值时间为401 (SD = 10)个体发生日,生长因子为4.0 (SD = 0.2)。相应参数的微小差异反映了从雅科夫列夫收集的材料中样本量小,而且相当缺乏出生后头三个十年的发育数据。因此,认为有必要将这些数据与其他人力资料来源的数据结合起来进行分析。从老鼠、猫和树鼩身上提取的人类和动物的生长参数进行了比较,揭示了大脑发育的差异。我们评估了Yakovlev收集的25个男性大脑与固定、包埋和染色相关的组织学萎缩。胎儿的大脑萎缩了约75%,成人的大脑萎缩了约50%。萎缩的程度与大脑的年龄成反比,而且个体差异也高达20%。因此,收缩必须在个体的基础上进行校正,以便通过组织学系列切片的形态计量学分析来确定大脑区域的真实生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brain growth in man.

25 male brains meeting the criteria for normativity and available in serial sections suitable for morphometric studies were selected from the Yakovlev Collection. Growth parameters were calculated based on the generalized logistic function. The ideal weight is 1,313 g (SD = 41), with a half value time of 387 (SD = 26) ontogenetic days and a growth factor of 4.0 (SD = 0.5). Comparison of growth parameters derived from a sample of 161 normative male brains collected at the Department of Neuroanatomy of the Medical School in Hannover revealed an ideal weight of 1,353 g (SD = 14), a half value time of 401 (SD = 10) ontogenetic days and a growth factor of 4.0 (SD = 0.2). The minor discrepancies in the corresponding parameters reflect the small sample size and a considerable lack of developmental data of the three first postnatal decades in the material derived from the Yakovlev Collection. It was, therefore, deemed necessary to analyze these data in combination with data derived from other sources of human material. A comparison of human with animal growth parameters derived from mice, cats and tree shrews reveals differences in brain development. Histological shrinkage of the 25 male brains of the Yakovlev Collection related to fixation, embedding, and staining was assessed. Fetal brains shrank by about 75%, and adult brains by about 50%. The degree of shrinkage was inversely proportional to the age of the brain and was also characterized by individual variations of up to 20%. Therefore, shrinkage had to be corrected on an individual basis in order to determine the true growth of brain regions as reflected by morphometric analysis of histological serial sections.

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