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Simulated dive in rats lead to acute changes in cerebral blood flow on MRI, but no cerebral injuries to grey or white matter
In this study, the effect of a simulated dive on rat brain was investigated using several magnetic resonance imaging (MRI)-methods and immunohistochemistry. Rats were randomly assigned to a dive- or a control group. The dive group was exposed to a simulated air dive to 600 kPa for 45 min. Pulmonary...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654193/ https://www.ncbi.nlm.nih.gov/pubmed/23232710 http://dx.doi.org/10.1007/s00421-012-2565-8 |
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author | Havnes, Marianne B. Widerøe, Marius Thuen, Marte Torp, Sverre H. Brubakk, Alf O. Møllerløkken, Andreas |
author_facet | Havnes, Marianne B. Widerøe, Marius Thuen, Marte Torp, Sverre H. Brubakk, Alf O. Møllerløkken, Andreas |
author_sort | Havnes, Marianne B. |
collection | PubMed |
description | In this study, the effect of a simulated dive on rat brain was investigated using several magnetic resonance imaging (MRI)-methods and immunohistochemistry. Rats were randomly assigned to a dive- or a control group. The dive group was exposed to a simulated air dive to 600 kPa for 45 min. Pulmonary artery was monitored for vascular gas bubbles by ultrasound. MRI was performed 1 h after decompression and at one and 2 weeks after the dive with a different combination of MRI sequences at each time point. Two weeks after decompression, rats were sacrificed and brains were prepared for histology. Dived rats had a different time-curve for the dynamic contrast-enhanced MRI signal than controls with higher relative signal intensity, a tendency towards longer time to peak and a larger area under the curve for the whole brain on the acute MRI scan. On MRI, 1 and 2 weeks after dive, T(2)-maps showed no signal abnormalities or morphological changes. However, region of interest based measurements of T(2) showed higher T(2) in the brain stem among decompressed animals than controls after one and 2 weeks. Microscopical examination including immunohistochemistry did not reveal apparent structural or cellular injuries in any part of the rat brains. These observations indicate that severe decompression does not seem to cause any structural or cellular injury to the brain tissue of the rat, but may cause circulatory changes in the brain perfusion in the acute phase. |
format | Online Article Text |
id | pubmed-3654193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-36541932013-05-16 Simulated dive in rats lead to acute changes in cerebral blood flow on MRI, but no cerebral injuries to grey or white matter Havnes, Marianne B. Widerøe, Marius Thuen, Marte Torp, Sverre H. Brubakk, Alf O. Møllerløkken, Andreas Eur J Appl Physiol Original Article In this study, the effect of a simulated dive on rat brain was investigated using several magnetic resonance imaging (MRI)-methods and immunohistochemistry. Rats were randomly assigned to a dive- or a control group. The dive group was exposed to a simulated air dive to 600 kPa for 45 min. Pulmonary artery was monitored for vascular gas bubbles by ultrasound. MRI was performed 1 h after decompression and at one and 2 weeks after the dive with a different combination of MRI sequences at each time point. Two weeks after decompression, rats were sacrificed and brains were prepared for histology. Dived rats had a different time-curve for the dynamic contrast-enhanced MRI signal than controls with higher relative signal intensity, a tendency towards longer time to peak and a larger area under the curve for the whole brain on the acute MRI scan. On MRI, 1 and 2 weeks after dive, T(2)-maps showed no signal abnormalities or morphological changes. However, region of interest based measurements of T(2) showed higher T(2) in the brain stem among decompressed animals than controls after one and 2 weeks. Microscopical examination including immunohistochemistry did not reveal apparent structural or cellular injuries in any part of the rat brains. These observations indicate that severe decompression does not seem to cause any structural or cellular injury to the brain tissue of the rat, but may cause circulatory changes in the brain perfusion in the acute phase. Springer-Verlag 2012-12-12 2013 /pmc/articles/PMC3654193/ /pubmed/23232710 http://dx.doi.org/10.1007/s00421-012-2565-8 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Havnes, Marianne B. Widerøe, Marius Thuen, Marte Torp, Sverre H. Brubakk, Alf O. Møllerløkken, Andreas Simulated dive in rats lead to acute changes in cerebral blood flow on MRI, but no cerebral injuries to grey or white matter |
title | Simulated dive in rats lead to acute changes in cerebral blood flow on MRI, but no cerebral injuries to grey or white matter |
title_full | Simulated dive in rats lead to acute changes in cerebral blood flow on MRI, but no cerebral injuries to grey or white matter |
title_fullStr | Simulated dive in rats lead to acute changes in cerebral blood flow on MRI, but no cerebral injuries to grey or white matter |
title_full_unstemmed | Simulated dive in rats lead to acute changes in cerebral blood flow on MRI, but no cerebral injuries to grey or white matter |
title_short | Simulated dive in rats lead to acute changes in cerebral blood flow on MRI, but no cerebral injuries to grey or white matter |
title_sort | simulated dive in rats lead to acute changes in cerebral blood flow on mri, but no cerebral injuries to grey or white matter |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654193/ https://www.ncbi.nlm.nih.gov/pubmed/23232710 http://dx.doi.org/10.1007/s00421-012-2565-8 |
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