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{"title":"Intracerebral Injections and Ultrastructural Analysis of High‐Pressure Frozen Brain Tissue","authors":"M. Weil, T. Ruhwedel, W. Möbius, M. Simons","doi":"10.1002/cpns.22","DOIUrl":null,"url":null,"abstract":"Intracerebral injections are an invasive method to bypass the blood brain barrier and are widely used to study molecular and cellular mechanisms of the central nervous system. The administered substances are injected directly at the site of interest, executing their effect locally. By combining injections in the rat brain with state‐of‐the‐art electron microscopy, subtle changes in ultrastructure of the nervous tissue can be detected prior to overt damage or disease. The protocol presented here involves stereotactic injection into the corpus callosum of Lewis rats and the cryopreparation of freshly dissected tissue for electron microscopy. The localization of the injection site in tissue sections during the sample preparation for transmission electron microscopy is explained and possible artifacts of the method are indicated. With the help of this powerful combination of injections and electron microscopy, subtle effects of the applied substances on the biology of neural cells can be identified and monitored over time. © 2017 by John Wiley & Sons, Inc.","PeriodicalId":40016,"journal":{"name":"Current Protocols in Neuroscience","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpns.22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Neuroscience","Score":null,"Total":0}
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高压冷冻脑组织的脑内注射和超微结构分析
脑内注射是一种绕过血脑屏障的侵入性方法,被广泛用于研究中枢神经系统的分子和细胞机制。给药物质直接注射到感兴趣的部位,局部发挥作用。通过将大鼠脑内注射与最先进的电子显微镜相结合,可以在明显损伤或疾病之前检测到神经组织超微结构的细微变化。本文提出的方案包括将立体定向注射到Lewis大鼠的胼胝体中,并将新鲜解剖的组织低温制备用于电子显微镜。在透射电子显微镜样品制备过程中,解释了组织切片中注射部位的定位,并指出了该方法可能产生的伪影。借助注射和电子显微镜的强大组合,可以识别和监测应用物质对神经细胞生物学的微妙影响。©2017 by John Wiley & Sons, Inc。
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