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{"title":"Intracerebral Injections and Ultrastructural Analysis of High-Pressure Frozen Brain Tissue","authors":"Marie-Theres Weil, Torben Ruhwedel, Wiebke Möbius, Mikael Simons","doi":"10.1002/cpns.22","DOIUrl":null,"url":null,"abstract":"<p>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.</p>","PeriodicalId":40016,"journal":{"name":"Current Protocols in Neuroscience","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2017-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpns.22","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/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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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.
高压冷冻脑组织的脑内注射及超微结构分析
脑内注射是一种绕过血脑屏障的侵入性方法,广泛用于研究中枢神经系统的分子和细胞机制。给药物质直接注射在感兴趣的部位,局部发挥作用。通过将大鼠大脑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向Lewis大鼠的胼胝体进行立体定向注射,并对新鲜解剖的组织进行冷冻修复以进行电子显微镜检查。解释了透射电子显微镜样品制备过程中组织切片中注射部位的定位,并指出了该方法可能存在的伪影。借助这种注射和电子显微镜的强大组合,可以随着时间的推移识别和监测所用物质对神经细胞生物学的细微影响。©2017 John Wiley&;股份有限公司。
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