| Literature DB >> 25504583 |
Hans F Wehrl1, Ilja Bezrukov2, Stefan Wiehr1, Mareike Lehnhoff1, Kerstin Fuchs1, Julia G Mannheim1, Leticia Quintanilla-Martinez3, Ursula Kohlhofer3, Manfred Kneilling4, Bernd J Pichler1, Alexander W Sauter5.
Abstract
Especially for neuroscience and the development of new biomarkers, a direct correlation between in vivo imaging and histology is essential. However, this comparison is hampered by deformation and shrinkage of tissue samples caused by fixation, dehydration and paraffin embedding. We used magnetic resonance (MR) imaging and computed tomography (CT) imaging to analyze the degree of shrinkage on murine brains for various fixatives. After in vivo imaging using 7 T MRI, animals were sacrificed and the brains were dissected and immediately placed in different fixatives, respectively: zinc-based fixative, neutral buffered formalin (NBF), paraformaldehyde (PFA), Bouin-Holland fixative and paraformaldehyde-lysine-periodate (PLP). The degree of shrinkage based on mouse brain volumes, radiodensity in Hounsfield units (HU), as well as non-linear deformations were obtained. The highest degree of shrinkage was observed for PLP (68.1%, P < 0.001), followed by PFA (60.2%, P<0.001) and NBF (58.6%, P<0.001). The zinc-based fixative revealed a low shrinkage with only 33.5% (P<0.001). Compared to NBF, the zinc-based fixative shows a slightly higher degree of deformations, but is still more homogenous than PFA. Tissue shrinkage can be monitored non-invasively with CT and MR. Zinc-based fixative causes the smallest degree of brain shrinkage and only small deformations and is therefore recommended for in vivo ex vivo comparison studies.Entities:
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Year: 2014 PMID: 25504583 DOI: 10.14670/HH-30.601
Source DB: PubMed Journal: Histol Histopathol ISSN: 0213-3911 Impact factor: 2.303