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Diffusion kurtosis imaging and pathological comparison of early hypoxic–ischemic brain damage in newborn piglets
To investigate the application value of magnetic resonance diffusion kurtosis imaging (DKI) in hypoxic–ischemic brain damage (HIBD) in newborn piglets and to compare imaging and pathological results. Of 36 piglets investigated, 18 were in the experimental group and 18 in the control group. The HIBD...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560608/ https://www.ncbi.nlm.nih.gov/pubmed/33057162 http://dx.doi.org/10.1038/s41598-020-74387-0 |
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author | Xiao, Juan He, Xiaoning Tian, Juan Chen, Honghai Liu, Jing Yang, Chao |
author_facet | Xiao, Juan He, Xiaoning Tian, Juan Chen, Honghai Liu, Jing Yang, Chao |
author_sort | Xiao, Juan |
collection | PubMed |
description | To investigate the application value of magnetic resonance diffusion kurtosis imaging (DKI) in hypoxic–ischemic brain damage (HIBD) in newborn piglets and to compare imaging and pathological results. Of 36 piglets investigated, 18 were in the experimental group and 18 in the control group. The HIBD model was established in newborn piglets by ligating the bilateral common carotid arteries and placing them into hypoxic chamber. All piglets underwent conventional MRI and DKI scans at 3, 6, 9, 12, 16, and 24 h postoperatively. Mean kurtosis (MK) and mean diffusivity (MD) maps were constructed. Then, the lesions were examined using light and electron microscopy and compared with DKI images. The MD value of the lesion area gradually decreased and the MK value gradually increased in the experimental group with time. The lesion areas gradually expanded with time; MK lesions were smaller than MD lesions. Light microscopy revealed neuronal swelling in the MK- and MD-matched and mismatched regions. Electron microscopy demonstrated obvious mitochondrial swelling and autophagosomes in the MK- and MD-matched region but normal mitochondrial morphology or mild swelling in the mismatched region. DKI can accurately evaluate early ischemic–hypoxic brain injury in newborn piglets. |
format | Online Article Text |
id | pubmed-7560608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75606082020-10-19 Diffusion kurtosis imaging and pathological comparison of early hypoxic–ischemic brain damage in newborn piglets Xiao, Juan He, Xiaoning Tian, Juan Chen, Honghai Liu, Jing Yang, Chao Sci Rep Article To investigate the application value of magnetic resonance diffusion kurtosis imaging (DKI) in hypoxic–ischemic brain damage (HIBD) in newborn piglets and to compare imaging and pathological results. Of 36 piglets investigated, 18 were in the experimental group and 18 in the control group. The HIBD model was established in newborn piglets by ligating the bilateral common carotid arteries and placing them into hypoxic chamber. All piglets underwent conventional MRI and DKI scans at 3, 6, 9, 12, 16, and 24 h postoperatively. Mean kurtosis (MK) and mean diffusivity (MD) maps were constructed. Then, the lesions were examined using light and electron microscopy and compared with DKI images. The MD value of the lesion area gradually decreased and the MK value gradually increased in the experimental group with time. The lesion areas gradually expanded with time; MK lesions were smaller than MD lesions. Light microscopy revealed neuronal swelling in the MK- and MD-matched and mismatched regions. Electron microscopy demonstrated obvious mitochondrial swelling and autophagosomes in the MK- and MD-matched region but normal mitochondrial morphology or mild swelling in the mismatched region. DKI can accurately evaluate early ischemic–hypoxic brain injury in newborn piglets. Nature Publishing Group UK 2020-10-14 /pmc/articles/PMC7560608/ /pubmed/33057162 http://dx.doi.org/10.1038/s41598-020-74387-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Xiao, Juan He, Xiaoning Tian, Juan Chen, Honghai Liu, Jing Yang, Chao Diffusion kurtosis imaging and pathological comparison of early hypoxic–ischemic brain damage in newborn piglets |
title | Diffusion kurtosis imaging and pathological comparison of early hypoxic–ischemic brain damage in newborn piglets |
title_full | Diffusion kurtosis imaging and pathological comparison of early hypoxic–ischemic brain damage in newborn piglets |
title_fullStr | Diffusion kurtosis imaging and pathological comparison of early hypoxic–ischemic brain damage in newborn piglets |
title_full_unstemmed | Diffusion kurtosis imaging and pathological comparison of early hypoxic–ischemic brain damage in newborn piglets |
title_short | Diffusion kurtosis imaging and pathological comparison of early hypoxic–ischemic brain damage in newborn piglets |
title_sort | diffusion kurtosis imaging and pathological comparison of early hypoxic–ischemic brain damage in newborn piglets |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560608/ https://www.ncbi.nlm.nih.gov/pubmed/33057162 http://dx.doi.org/10.1038/s41598-020-74387-0 |
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