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Offspring of rats with cerebral hypoxia-ischemia manifest cognitive dysfunction in learning and memory abilities
Neonatal hypoxic-ischemic encephalopathy is a serious neurological disease, often resulting in long-term neurodevelopmental disorders among surviving children. However, whether these neurodevelopmental issues can be passed to offspring remains unclear. The right common carotid artery of 7-day-old pa...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437586/ https://www.ncbi.nlm.nih.gov/pubmed/32209770 http://dx.doi.org/10.4103/1673-5374.276359 |
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author | Xue, Lu-Lu Wang, Fang Niu, Rui-Ze Tan, Ya-Xin Liu, Jia Jin, Yuan Ma, Zheng Zhang, Zi-Bin Jiang, Ya Chen, Li Xia, Qing-Jie Chen, Jun-Jie Wang, Ting-Hua Xiong, Liu-Lin |
author_facet | Xue, Lu-Lu Wang, Fang Niu, Rui-Ze Tan, Ya-Xin Liu, Jia Jin, Yuan Ma, Zheng Zhang, Zi-Bin Jiang, Ya Chen, Li Xia, Qing-Jie Chen, Jun-Jie Wang, Ting-Hua Xiong, Liu-Lin |
author_sort | Xue, Lu-Lu |
collection | PubMed |
description | Neonatal hypoxic-ischemic encephalopathy is a serious neurological disease, often resulting in long-term neurodevelopmental disorders among surviving children. However, whether these neurodevelopmental issues can be passed to offspring remains unclear. The right common carotid artery of 7-day-old parental-generation rats was subjected to permanent ligation using a vessel electrocoagulator. Neonatal hypoxic-ischemic rat models were established by subjecting the rats to 8% O(2)–92% N(2) for 2 hours. The results showed that 24 hours after hypoxia and ischemia, pathological damage, cerebral atrophy, liquefaction, and impairment were found, and Zea-Longa scores were significantly increased. The parental-generation rats were propagated at 3 months old, and offspring were obtained. No changes in the overall brain structures of these offspring rats were identified by magnetic resonance imaging. However, the escape latency was longer and the number of platform crossings was reduced among these offspring compared with normal rats. These results indicated that the offspring of hypoxic-ischemic encephalopathy model rats displayed cognitive impairments in learning and memory. This study was approved by the Animal Care & Welfare Committee of Kunming Medical University, China in 2018 (approval No. kmmu2019072). |
format | Online Article Text |
id | pubmed-7437586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-74375862020-08-28 Offspring of rats with cerebral hypoxia-ischemia manifest cognitive dysfunction in learning and memory abilities Xue, Lu-Lu Wang, Fang Niu, Rui-Ze Tan, Ya-Xin Liu, Jia Jin, Yuan Ma, Zheng Zhang, Zi-Bin Jiang, Ya Chen, Li Xia, Qing-Jie Chen, Jun-Jie Wang, Ting-Hua Xiong, Liu-Lin Neural Regen Res Research Article Neonatal hypoxic-ischemic encephalopathy is a serious neurological disease, often resulting in long-term neurodevelopmental disorders among surviving children. However, whether these neurodevelopmental issues can be passed to offspring remains unclear. The right common carotid artery of 7-day-old parental-generation rats was subjected to permanent ligation using a vessel electrocoagulator. Neonatal hypoxic-ischemic rat models were established by subjecting the rats to 8% O(2)–92% N(2) for 2 hours. The results showed that 24 hours after hypoxia and ischemia, pathological damage, cerebral atrophy, liquefaction, and impairment were found, and Zea-Longa scores were significantly increased. The parental-generation rats were propagated at 3 months old, and offspring were obtained. No changes in the overall brain structures of these offspring rats were identified by magnetic resonance imaging. However, the escape latency was longer and the number of platform crossings was reduced among these offspring compared with normal rats. These results indicated that the offspring of hypoxic-ischemic encephalopathy model rats displayed cognitive impairments in learning and memory. This study was approved by the Animal Care & Welfare Committee of Kunming Medical University, China in 2018 (approval No. kmmu2019072). Wolters Kluwer - Medknow 2020-02-28 /pmc/articles/PMC7437586/ /pubmed/32209770 http://dx.doi.org/10.4103/1673-5374.276359 Text en Copyright: © 2020 Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Xue, Lu-Lu Wang, Fang Niu, Rui-Ze Tan, Ya-Xin Liu, Jia Jin, Yuan Ma, Zheng Zhang, Zi-Bin Jiang, Ya Chen, Li Xia, Qing-Jie Chen, Jun-Jie Wang, Ting-Hua Xiong, Liu-Lin Offspring of rats with cerebral hypoxia-ischemia manifest cognitive dysfunction in learning and memory abilities |
title | Offspring of rats with cerebral hypoxia-ischemia manifest cognitive dysfunction in learning and memory abilities |
title_full | Offspring of rats with cerebral hypoxia-ischemia manifest cognitive dysfunction in learning and memory abilities |
title_fullStr | Offspring of rats with cerebral hypoxia-ischemia manifest cognitive dysfunction in learning and memory abilities |
title_full_unstemmed | Offspring of rats with cerebral hypoxia-ischemia manifest cognitive dysfunction in learning and memory abilities |
title_short | Offspring of rats with cerebral hypoxia-ischemia manifest cognitive dysfunction in learning and memory abilities |
title_sort | offspring of rats with cerebral hypoxia-ischemia manifest cognitive dysfunction in learning and memory abilities |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437586/ https://www.ncbi.nlm.nih.gov/pubmed/32209770 http://dx.doi.org/10.4103/1673-5374.276359 |
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