Department of Pathological Anatomy and Forensic Medicine, University of Tartu, 19 Ravila Street, 50411 Tartu, Estonia; Estonian Forensic Science Institute, Tervise 20, Tallinn, Estonia.
Department of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia; Centre of Excellence in Genomics and Translational Medicine, University of Tartu, Tartu, Estonia.
J Neurosci Methods. 2024 Apr;404:110059. doi: 10.1016/j.jneumeth.2024.110059. Epub 2024 Jan 11.
Chemical fixation of the brain can be executed through either the immersion method or the perfusion method. Perfusion fixation allows for better preservation of the brain tissue's ultrastructure, as it provides rapid and uniform delivery of the fixative to the tissue. Still, not all facilities have the expertise to perform perfusion fixation, with initial high cost and complexity of perfusion systems as the main factors limiting its widespread usage.
Here we present our low-cost approach of whole brain ex situ perfusion fixation to overcome the aforementioned limitations. Our self-made perfusion system, constructed utilising commercially accessible and affordable medical resources alongside laboratory and everyday items, demonstrates the capability to generate superior histological stainings of brain tissue. The perfused tissue can be stored prior to proceeding with IHC for at least one year.
Our method yielded high-quality results in histological stainings using both free-floating cryosections and paraffin-embedded tissue sections. The system is fully reusable and complies with the principles of sustainable management.
Our whole brain perfusion system has been assembled from simple components and is able to achieve a linear flow with a pressure of 70 mmHg corresponding to the perfusion pressure of the brain.
Our ex situ method can be especially useful in research settings where expensive perfusion systems are not affordable or in any field with high time pressure, making it suitable for the field of forensic medicine or pathology in general.
脑的化学固定可以通过浸浴法或灌流法来执行。灌流固定可以更好地保存脑组织的超微结构,因为它可以快速且均匀地将固定剂输送到组织中。尽管如此,并非所有的设施都有进行灌流固定的专业知识,其初始高成本和灌流系统的复杂性是限制其广泛应用的主要因素。
在这里,我们提出了一种低成本的全脑离体灌流固定方法,以克服上述限制。我们自制的灌流系统利用商业上可获得且负担得起的医疗资源以及实验室和日常用品来构建,证明了能够生成脑组织的卓越组织学染色。在进行免疫组织化学之前,可将灌注的组织储存至少一年。
我们的方法在使用游离冷冻切片和石蜡包埋组织切片进行组织学染色时均产生了高质量的结果。该系统是完全可重复使用的,并符合可持续管理的原则。
我们的全脑灌流系统由简单的组件组装而成,能够实现线性流动,压力为 70mmHg,相当于大脑的灌注压力。
我们的离体方法在那些昂贵的灌流系统不可负担或时间压力大的研究环境中特别有用,因此适用于一般法医学或病理学领域。