Cargando…
A multiscale tissue assessment in a rat model of mild traumatic brain injury
Diffusion tensor imaging (DTI) has demonstrated the potential to assess the pathophysiology of mild traumatic brain injury (mTBI) but correlations of DTI findings and pathological changes in mTBI are unclear. We evaluated the potential of ex vivo DTI to detect tissue damage in a mild mTBI rat model...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764078/ https://www.ncbi.nlm.nih.gov/pubmed/36331507 http://dx.doi.org/10.1093/jnen/nlac100 |
_version_ | 1784853199080914944 |
---|---|
author | San Martín Molina, Isabel Fratini, Michela Campi, Gaetano Burghammer, Manfred Grünewald, Tilman A Salo, Raimo A Narvaez, Omar Aggarwal, Manisha Tohka, Jussi Sierra, Alejandra |
author_facet | San Martín Molina, Isabel Fratini, Michela Campi, Gaetano Burghammer, Manfred Grünewald, Tilman A Salo, Raimo A Narvaez, Omar Aggarwal, Manisha Tohka, Jussi Sierra, Alejandra |
author_sort | San Martín Molina, Isabel |
collection | PubMed |
description | Diffusion tensor imaging (DTI) has demonstrated the potential to assess the pathophysiology of mild traumatic brain injury (mTBI) but correlations of DTI findings and pathological changes in mTBI are unclear. We evaluated the potential of ex vivo DTI to detect tissue damage in a mild mTBI rat model by exploiting multiscale imaging methods, histology and scanning micro-X-ray diffraction (SμXRD) 35 days after sham-operation (n = 2) or mTBI (n = 3). There were changes in DTI parameters rostral to the injury site. When examined by histology and SμXRD, there was evidence of axonal damage, reduced myelin density, gliosis, and ultrastructural alterations in myelin that were ongoing at the experimental time point of 35 days postinjury. We assessed the relationship between the 3 imaging modalities by multiple linear regression analysis. In this analysis, DTI and histological parameters were moderately related, whereas SμXRD parameters correlated weakly with DTI and histology. These findings suggest that while DTI appears to distinguish tissue changes at the microstructural level related to the loss of myelinated axons and gliosis, its ability to visualize alterations in myelin ultrastructure is limited. The use of several imaging techniques represents a novel approach to reveal tissue damage and provides new insights into mTBI detection. |
format | Online Article Text |
id | pubmed-9764078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-97640782022-12-20 A multiscale tissue assessment in a rat model of mild traumatic brain injury San Martín Molina, Isabel Fratini, Michela Campi, Gaetano Burghammer, Manfred Grünewald, Tilman A Salo, Raimo A Narvaez, Omar Aggarwal, Manisha Tohka, Jussi Sierra, Alejandra J Neuropathol Exp Neurol Original Article Diffusion tensor imaging (DTI) has demonstrated the potential to assess the pathophysiology of mild traumatic brain injury (mTBI) but correlations of DTI findings and pathological changes in mTBI are unclear. We evaluated the potential of ex vivo DTI to detect tissue damage in a mild mTBI rat model by exploiting multiscale imaging methods, histology and scanning micro-X-ray diffraction (SμXRD) 35 days after sham-operation (n = 2) or mTBI (n = 3). There were changes in DTI parameters rostral to the injury site. When examined by histology and SμXRD, there was evidence of axonal damage, reduced myelin density, gliosis, and ultrastructural alterations in myelin that were ongoing at the experimental time point of 35 days postinjury. We assessed the relationship between the 3 imaging modalities by multiple linear regression analysis. In this analysis, DTI and histological parameters were moderately related, whereas SμXRD parameters correlated weakly with DTI and histology. These findings suggest that while DTI appears to distinguish tissue changes at the microstructural level related to the loss of myelinated axons and gliosis, its ability to visualize alterations in myelin ultrastructure is limited. The use of several imaging techniques represents a novel approach to reveal tissue damage and provides new insights into mTBI detection. Oxford University Press 2022-11-04 /pmc/articles/PMC9764078/ /pubmed/36331507 http://dx.doi.org/10.1093/jnen/nlac100 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of American Association of Neuropathologists, Inc. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article San Martín Molina, Isabel Fratini, Michela Campi, Gaetano Burghammer, Manfred Grünewald, Tilman A Salo, Raimo A Narvaez, Omar Aggarwal, Manisha Tohka, Jussi Sierra, Alejandra A multiscale tissue assessment in a rat model of mild traumatic brain injury |
title | A multiscale tissue assessment in a rat model of mild traumatic brain injury |
title_full | A multiscale tissue assessment in a rat model of mild traumatic brain injury |
title_fullStr | A multiscale tissue assessment in a rat model of mild traumatic brain injury |
title_full_unstemmed | A multiscale tissue assessment in a rat model of mild traumatic brain injury |
title_short | A multiscale tissue assessment in a rat model of mild traumatic brain injury |
title_sort | multiscale tissue assessment in a rat model of mild traumatic brain injury |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764078/ https://www.ncbi.nlm.nih.gov/pubmed/36331507 http://dx.doi.org/10.1093/jnen/nlac100 |
work_keys_str_mv | AT sanmartinmolinaisabel amultiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT fratinimichela amultiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT campigaetano amultiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT burghammermanfred amultiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT grunewaldtilmana amultiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT saloraimoa amultiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT narvaezomar amultiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT aggarwalmanisha amultiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT tohkajussi amultiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT sierraalejandra amultiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT sanmartinmolinaisabel multiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT fratinimichela multiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT campigaetano multiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT burghammermanfred multiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT grunewaldtilmana multiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT saloraimoa multiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT narvaezomar multiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT aggarwalmanisha multiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT tohkajussi multiscaletissueassessmentinaratmodelofmildtraumaticbraininjury AT sierraalejandra multiscaletissueassessmentinaratmodelofmildtraumaticbraininjury |