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Caffeine Restores Neuronal Damage and Inflammatory Response in a Model of Intraventricular Hemorrhage of the Preterm Newborn

Germinal matrix-intraventricular hemorrhage (GM-IVH) is the most frequent intracranial hemorrhage in the preterm infant (PT). Long-term GM-IVH-associated sequelae include cerebral palsy, sensory and motor impairment, learning disabilities, or neuropsychiatric disorders. The societal and health burde...

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Autores principales: Alves-Martinez, Pilar, Atienza-Navarro, Isabel, Vargas-Soria, Maria, Carranza-Naval, Maria Jose, Infante-Garcia, Carmen, Benavente-Fernandez, Isabel, Del Marco, Angel, Lubian-Lopez, Simon, Garcia-Alloza, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411947/
https://www.ncbi.nlm.nih.gov/pubmed/36035990
http://dx.doi.org/10.3389/fcell.2022.908045
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author Alves-Martinez, Pilar
Atienza-Navarro, Isabel
Vargas-Soria, Maria
Carranza-Naval, Maria Jose
Infante-Garcia, Carmen
Benavente-Fernandez, Isabel
Del Marco, Angel
Lubian-Lopez, Simon
Garcia-Alloza, Monica
author_facet Alves-Martinez, Pilar
Atienza-Navarro, Isabel
Vargas-Soria, Maria
Carranza-Naval, Maria Jose
Infante-Garcia, Carmen
Benavente-Fernandez, Isabel
Del Marco, Angel
Lubian-Lopez, Simon
Garcia-Alloza, Monica
author_sort Alves-Martinez, Pilar
collection PubMed
description Germinal matrix-intraventricular hemorrhage (GM-IVH) is the most frequent intracranial hemorrhage in the preterm infant (PT). Long-term GM-IVH-associated sequelae include cerebral palsy, sensory and motor impairment, learning disabilities, or neuropsychiatric disorders. The societal and health burden associated with GM-IVH is worsened by the fact that there is no successful treatment to limit or reduce brain damage and neurodevelopment disabilities. Caffeine (Caf) is a methylxanthine that binds to adenosine receptors, regularly used to treat the apnea of prematurity. While previous studies support the beneficial effects at the brain level of Caf in PT, there are no studies that specifically focus on the role of Caf in GM-IVH. Therefore, to further understand the role of Caf in GM-IVH, we have analyzed two doses of Caf (10 and 20 mg/kg) in a murine model of the disease. We have analyzed the short (P14) and long (P70) effects of the treatment on brain atrophy and neuron wellbeing, including density, curvature, and phospho-tau/total tau ratio. We have analyzed proliferation and neurogenesis, as well as microglia and hemorrhage burdens. We have also assessed the long-term effects of Caf treatment at cognitive level. To induce GM-IVH, we have administered intraventricular collagenase to P7 CD1 mice and have analyzed these animals in the short (P14) and long (P70) term. Caf showed a general neuroprotective effect in our model of GM-IVH of the PT. In our study, Caf administration diminishes brain atrophy and ventricle enlargement. Likewise, Caf limits neuronal damage, including neurite curvature and tau phosphorylation. It also contributes to maintaining neurogenesis in the subventricular zone, a neurogenic niche that is severely affected after GM-IVH. Furthermore, Caf ameliorates small vessel bleeding and inflammation in both the cortex and the subventricular zone. Observed mitigation of brain pathological features commonly associated with GM-IVH also results in a significant improvement of learning and memory abilities in the long term. Altogether, our data support the promising effects of Caf to reduce central nervous system complications associated with GM-IVH.
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spelling pubmed-94119472022-08-27 Caffeine Restores Neuronal Damage and Inflammatory Response in a Model of Intraventricular Hemorrhage of the Preterm Newborn Alves-Martinez, Pilar Atienza-Navarro, Isabel Vargas-Soria, Maria Carranza-Naval, Maria Jose Infante-Garcia, Carmen Benavente-Fernandez, Isabel Del Marco, Angel Lubian-Lopez, Simon Garcia-Alloza, Monica Front Cell Dev Biol Cell and Developmental Biology Germinal matrix-intraventricular hemorrhage (GM-IVH) is the most frequent intracranial hemorrhage in the preterm infant (PT). Long-term GM-IVH-associated sequelae include cerebral palsy, sensory and motor impairment, learning disabilities, or neuropsychiatric disorders. The societal and health burden associated with GM-IVH is worsened by the fact that there is no successful treatment to limit or reduce brain damage and neurodevelopment disabilities. Caffeine (Caf) is a methylxanthine that binds to adenosine receptors, regularly used to treat the apnea of prematurity. While previous studies support the beneficial effects at the brain level of Caf in PT, there are no studies that specifically focus on the role of Caf in GM-IVH. Therefore, to further understand the role of Caf in GM-IVH, we have analyzed two doses of Caf (10 and 20 mg/kg) in a murine model of the disease. We have analyzed the short (P14) and long (P70) effects of the treatment on brain atrophy and neuron wellbeing, including density, curvature, and phospho-tau/total tau ratio. We have analyzed proliferation and neurogenesis, as well as microglia and hemorrhage burdens. We have also assessed the long-term effects of Caf treatment at cognitive level. To induce GM-IVH, we have administered intraventricular collagenase to P7 CD1 mice and have analyzed these animals in the short (P14) and long (P70) term. Caf showed a general neuroprotective effect in our model of GM-IVH of the PT. In our study, Caf administration diminishes brain atrophy and ventricle enlargement. Likewise, Caf limits neuronal damage, including neurite curvature and tau phosphorylation. It also contributes to maintaining neurogenesis in the subventricular zone, a neurogenic niche that is severely affected after GM-IVH. Furthermore, Caf ameliorates small vessel bleeding and inflammation in both the cortex and the subventricular zone. Observed mitigation of brain pathological features commonly associated with GM-IVH also results in a significant improvement of learning and memory abilities in the long term. Altogether, our data support the promising effects of Caf to reduce central nervous system complications associated with GM-IVH. Frontiers Media S.A. 2022-08-12 /pmc/articles/PMC9411947/ /pubmed/36035990 http://dx.doi.org/10.3389/fcell.2022.908045 Text en Copyright © 2022 Alves-Martinez, Atienza-Navarro, Vargas-Soria, Carranza-Naval, Infante-Garcia, Benavente-Fernandez, Del Marco, Lubian-Lopez and Garcia-Alloza. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Alves-Martinez, Pilar
Atienza-Navarro, Isabel
Vargas-Soria, Maria
Carranza-Naval, Maria Jose
Infante-Garcia, Carmen
Benavente-Fernandez, Isabel
Del Marco, Angel
Lubian-Lopez, Simon
Garcia-Alloza, Monica
Caffeine Restores Neuronal Damage and Inflammatory Response in a Model of Intraventricular Hemorrhage of the Preterm Newborn
title Caffeine Restores Neuronal Damage and Inflammatory Response in a Model of Intraventricular Hemorrhage of the Preterm Newborn
title_full Caffeine Restores Neuronal Damage and Inflammatory Response in a Model of Intraventricular Hemorrhage of the Preterm Newborn
title_fullStr Caffeine Restores Neuronal Damage and Inflammatory Response in a Model of Intraventricular Hemorrhage of the Preterm Newborn
title_full_unstemmed Caffeine Restores Neuronal Damage and Inflammatory Response in a Model of Intraventricular Hemorrhage of the Preterm Newborn
title_short Caffeine Restores Neuronal Damage and Inflammatory Response in a Model of Intraventricular Hemorrhage of the Preterm Newborn
title_sort caffeine restores neuronal damage and inflammatory response in a model of intraventricular hemorrhage of the preterm newborn
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411947/
https://www.ncbi.nlm.nih.gov/pubmed/36035990
http://dx.doi.org/10.3389/fcell.2022.908045
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