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用扫描电子显微镜观察脑微血管的三维结构:一种适用于胎鼠和成年大鼠的脑血管铸型方法。

Three-dimensional architecture of cerebral microvessels with a scanning electron microscope: a cerebrovascular casting method for fetal and adult rats.

作者信息

Yoshida Y, Ikuta F

出版信息

J Cereb Blood Flow Metab. 1984 Jun;4(2):290-6. doi: 10.1038/jcbfm.1984.40.

DOI:10.1038/jcbfm.1984.40
PMID:6725439
Abstract

Vascular casting for scanning electron microscopic studies on microvascular architecture is in common use for various visceral organs in the field of anatomy. However, only a few studies have been performed on the brain using the previously reported casting method, and no detailed descriptions deal with suitable methodology for producing brain vascular casts. Our casting method, introduced here, for the CNS from the fetal to the adult stage involves the following modifications: (1) Perfusion fixation of the brain is carried out before injecting the plastic resin for casting into the cerebral blood vessels; (2) digestion of nervous tissue is accomplished with a sodium hydroxide and sodium hypochlorite solution; and (3) vascular casts are dried by a freeze-drying method, while the nondigested brain slices opposite the casts can be investigated with light microscopy and transmission electron microscopy. This modified casting method enables one to represent the microvascular system of the rat brain three-dimensionally from embryonal day 17 onward. It is hoped that this method will prove to be a useful tool in morphological vascular research on the nervous system.

摘要

血管铸型用于扫描电子显微镜研究微血管结构,在解剖学领域中常用于各种内脏器官。然而,使用先前报道的铸型方法对大脑进行的研究较少,并且没有详细描述生产脑血管铸型的合适方法。我们在此介绍的从胎儿到成年阶段的中枢神经系统铸型方法包括以下改进:(1)在将用于铸型的塑料树脂注入脑血管之前,先对大脑进行灌注固定;(2)用氢氧化钠和次氯酸钠溶液消化神经组织;(3)血管铸型通过冷冻干燥法干燥,而与铸型相对的未消化脑切片可用于光学显微镜和透射电子显微镜检查。这种改进的铸型方法能够从胚胎第17天起三维呈现大鼠大脑的微血管系统。希望这种方法将被证明是神经系统形态血管研究中的一种有用工具。

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Three-dimensional architecture of cerebral microvessels with a scanning electron microscope: a cerebrovascular casting method for fetal and adult rats.用扫描电子显微镜观察脑微血管的三维结构:一种适用于胎鼠和成年大鼠的脑血管铸型方法。
J Cereb Blood Flow Metab. 1984 Jun;4(2):290-6. doi: 10.1038/jcbfm.1984.40.
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