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Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury
BACKGROUND: The administration of supplemental oxygen to treat ventilatory insufficiency may lead to the formation of reactive oxygen species and subsequent tissue damage. Cytochrome P4501A1 (CYP1A1) can modulate hyperoxic lung injury by a currently unknown mechanism. Our objective was to evaluate t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002203/ https://www.ncbi.nlm.nih.gov/pubmed/27567616 http://dx.doi.org/10.1186/s12967-016-1009-3 |
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author | Richter, Jute Jimenez, Julio Nagatomo, Taro Toelen, Jaan Brady, Paul Salaets, Thomas Lesage, Flore Vanoirbeek, Jeroen Deprest, Jan |
author_facet | Richter, Jute Jimenez, Julio Nagatomo, Taro Toelen, Jaan Brady, Paul Salaets, Thomas Lesage, Flore Vanoirbeek, Jeroen Deprest, Jan |
author_sort | Richter, Jute |
collection | PubMed |
description | BACKGROUND: The administration of supplemental oxygen to treat ventilatory insufficiency may lead to the formation of reactive oxygen species and subsequent tissue damage. Cytochrome P4501A1 (CYP1A1) can modulate hyperoxic lung injury by a currently unknown mechanism. Our objective was to evaluate the effect of administration of omeprazole on the induction of CYP1A1 and its influence on hyperoxic lung injury in an established preterm rabbit model. METHODS: Omeprazole was administered either (1) directly to the fetus, (2) to the mother or (3) after birth to the pups in different doses (2–10 or 20 mg/kg). Controls were injected with the same amount of saline. Pups were housed in normoxia (21 %) or hyperoxia (>95 %) for 5 days. Outcome parameters were induction of CYP1A1 measured by real-time polymerase chain reaction (RT-PCR) immediately after delivery, at day 3 and day 5 as well as lung function, morphometry and immunohistochemistry assessed at day 5 of life. Transcriptome analysis was used to define the targeted pathways. RESULTS: Daily neonatal injections demonstrated a dose-dependent increase in CYP1A1. Lung function tests showed a significant improvement in tissue damping, tissue elasticity, total lung capacity, static compliance and elastance. Morphometry revealed a more developed lung architecture with thinned septae in animals treated with the highest dose (20 mg/kg) of omeprazole. Surfactant protein B, vascular endothelial growth factor and its receptor were significantly increased on immunohistochemical stainings after omeprazole treatment. CONCLUSIONS: Neonatal administration of omeprazole induces CYP1A1 in a dose-dependent matter and combined pre- and postnatal administration attenuates hyperoxic lung injury in preterm rabbits, even with the lowest dose of omeprazole without clear CYP1A1 induction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12967-016-1009-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5002203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50022032016-08-28 Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury Richter, Jute Jimenez, Julio Nagatomo, Taro Toelen, Jaan Brady, Paul Salaets, Thomas Lesage, Flore Vanoirbeek, Jeroen Deprest, Jan J Transl Med Research BACKGROUND: The administration of supplemental oxygen to treat ventilatory insufficiency may lead to the formation of reactive oxygen species and subsequent tissue damage. Cytochrome P4501A1 (CYP1A1) can modulate hyperoxic lung injury by a currently unknown mechanism. Our objective was to evaluate the effect of administration of omeprazole on the induction of CYP1A1 and its influence on hyperoxic lung injury in an established preterm rabbit model. METHODS: Omeprazole was administered either (1) directly to the fetus, (2) to the mother or (3) after birth to the pups in different doses (2–10 or 20 mg/kg). Controls were injected with the same amount of saline. Pups were housed in normoxia (21 %) or hyperoxia (>95 %) for 5 days. Outcome parameters were induction of CYP1A1 measured by real-time polymerase chain reaction (RT-PCR) immediately after delivery, at day 3 and day 5 as well as lung function, morphometry and immunohistochemistry assessed at day 5 of life. Transcriptome analysis was used to define the targeted pathways. RESULTS: Daily neonatal injections demonstrated a dose-dependent increase in CYP1A1. Lung function tests showed a significant improvement in tissue damping, tissue elasticity, total lung capacity, static compliance and elastance. Morphometry revealed a more developed lung architecture with thinned septae in animals treated with the highest dose (20 mg/kg) of omeprazole. Surfactant protein B, vascular endothelial growth factor and its receptor were significantly increased on immunohistochemical stainings after omeprazole treatment. CONCLUSIONS: Neonatal administration of omeprazole induces CYP1A1 in a dose-dependent matter and combined pre- and postnatal administration attenuates hyperoxic lung injury in preterm rabbits, even with the lowest dose of omeprazole without clear CYP1A1 induction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12967-016-1009-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-27 /pmc/articles/PMC5002203/ /pubmed/27567616 http://dx.doi.org/10.1186/s12967-016-1009-3 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Richter, Jute Jimenez, Julio Nagatomo, Taro Toelen, Jaan Brady, Paul Salaets, Thomas Lesage, Flore Vanoirbeek, Jeroen Deprest, Jan Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury |
title | Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury |
title_full | Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury |
title_fullStr | Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury |
title_full_unstemmed | Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury |
title_short | Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury |
title_sort | proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002203/ https://www.ncbi.nlm.nih.gov/pubmed/27567616 http://dx.doi.org/10.1186/s12967-016-1009-3 |
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