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Severe intraventricular hemorrhage causes long-lasting structural damage in a preterm rabbit pup model
BACKGROUND: Intraventricular hemorrhage causes significant lifelong mortality and morbidity, especially in preterm born infants. Progress in finding an effective therapy is stymied by a lack of preterm animal models with long-term follow-up. This study addresses this unmet need, using an established...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9522590/ https://www.ncbi.nlm.nih.gov/pubmed/35505079 http://dx.doi.org/10.1038/s41390-022-02075-y |
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author | Romantsik, Olga Ross-Munro, Emily Grönlund, Susanne Holmqvist, Bo Brinte, Anders Gerdtsson, Erik Vallius, Suvi Bruschettini, Matteo Wang, Xiaoyang Fleiss, Bobbi Ley, David |
author_facet | Romantsik, Olga Ross-Munro, Emily Grönlund, Susanne Holmqvist, Bo Brinte, Anders Gerdtsson, Erik Vallius, Suvi Bruschettini, Matteo Wang, Xiaoyang Fleiss, Bobbi Ley, David |
author_sort | Romantsik, Olga |
collection | PubMed |
description | BACKGROUND: Intraventricular hemorrhage causes significant lifelong mortality and morbidity, especially in preterm born infants. Progress in finding an effective therapy is stymied by a lack of preterm animal models with long-term follow-up. This study addresses this unmet need, using an established model of preterm rabbit IVH and analyzing outcomes out to 1 month of age. METHODS: Rabbit pups were delivered preterm and administered intraperitoneal injection of glycerol at 3 h of life and approximately 58% developed IVH. Neurobehavioral assessment was performed at 1 month of age followed by immunohistochemical labeling of epitopes for neurons, synapses, myelination, and interneurons, analyzed by means of digital quantitation and assessed via two-way ANOVA or Student’s t test. RESULTS: IVH pups had globally reduced myelin content, an aberrant cortical myelination microstructure, and thinner upper cortical layers (I–III). We also observed a lower number of parvalbumin (PV)-positive interneurons in deeper cortical layers (IV–VI) in IVH animals and reduced numbers of neurons, synapses, and microglia. However, there were no discernable changes in behaviors. CONCLUSIONS: We have established in this preterm pup model that long-term changes after IVH include significant wide-ranging alterations to cortical organization and microstructure. Further work to improve the sensitivity of neurocognitive testing in this species at this age may be required. IMPACT: This study uses an established animal model of preterm birth, in which the rabbit pups are truly born preterm, with reduced organ maturation and deprivation of maternally supplied trophic factors. This is the first study in preterm rabbits that explores the impacts of severe intraventricular hemorrhage beyond 14 days, out to 1 month of age. Our finding of persisting but subtle global changes including brain white and gray matter will have impact on our understanding of the best path for therapy design and interventions. |
format | Online Article Text |
id | pubmed-9522590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-95225902022-10-01 Severe intraventricular hemorrhage causes long-lasting structural damage in a preterm rabbit pup model Romantsik, Olga Ross-Munro, Emily Grönlund, Susanne Holmqvist, Bo Brinte, Anders Gerdtsson, Erik Vallius, Suvi Bruschettini, Matteo Wang, Xiaoyang Fleiss, Bobbi Ley, David Pediatr Res Basic Science Article BACKGROUND: Intraventricular hemorrhage causes significant lifelong mortality and morbidity, especially in preterm born infants. Progress in finding an effective therapy is stymied by a lack of preterm animal models with long-term follow-up. This study addresses this unmet need, using an established model of preterm rabbit IVH and analyzing outcomes out to 1 month of age. METHODS: Rabbit pups were delivered preterm and administered intraperitoneal injection of glycerol at 3 h of life and approximately 58% developed IVH. Neurobehavioral assessment was performed at 1 month of age followed by immunohistochemical labeling of epitopes for neurons, synapses, myelination, and interneurons, analyzed by means of digital quantitation and assessed via two-way ANOVA or Student’s t test. RESULTS: IVH pups had globally reduced myelin content, an aberrant cortical myelination microstructure, and thinner upper cortical layers (I–III). We also observed a lower number of parvalbumin (PV)-positive interneurons in deeper cortical layers (IV–VI) in IVH animals and reduced numbers of neurons, synapses, and microglia. However, there were no discernable changes in behaviors. CONCLUSIONS: We have established in this preterm pup model that long-term changes after IVH include significant wide-ranging alterations to cortical organization and microstructure. Further work to improve the sensitivity of neurocognitive testing in this species at this age may be required. IMPACT: This study uses an established animal model of preterm birth, in which the rabbit pups are truly born preterm, with reduced organ maturation and deprivation of maternally supplied trophic factors. This is the first study in preterm rabbits that explores the impacts of severe intraventricular hemorrhage beyond 14 days, out to 1 month of age. Our finding of persisting but subtle global changes including brain white and gray matter will have impact on our understanding of the best path for therapy design and interventions. Nature Publishing Group US 2022-05-03 2022 /pmc/articles/PMC9522590/ /pubmed/35505079 http://dx.doi.org/10.1038/s41390-022-02075-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Basic Science Article Romantsik, Olga Ross-Munro, Emily Grönlund, Susanne Holmqvist, Bo Brinte, Anders Gerdtsson, Erik Vallius, Suvi Bruschettini, Matteo Wang, Xiaoyang Fleiss, Bobbi Ley, David Severe intraventricular hemorrhage causes long-lasting structural damage in a preterm rabbit pup model |
title | Severe intraventricular hemorrhage causes long-lasting structural damage in a preterm rabbit pup model |
title_full | Severe intraventricular hemorrhage causes long-lasting structural damage in a preterm rabbit pup model |
title_fullStr | Severe intraventricular hemorrhage causes long-lasting structural damage in a preterm rabbit pup model |
title_full_unstemmed | Severe intraventricular hemorrhage causes long-lasting structural damage in a preterm rabbit pup model |
title_short | Severe intraventricular hemorrhage causes long-lasting structural damage in a preterm rabbit pup model |
title_sort | severe intraventricular hemorrhage causes long-lasting structural damage in a preterm rabbit pup model |
topic | Basic Science Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9522590/ https://www.ncbi.nlm.nih.gov/pubmed/35505079 http://dx.doi.org/10.1038/s41390-022-02075-y |
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