Cargando…
Small Molecule Inhibitor Adjuvant Surfactant Therapy Attenuates Ventilator- and Hyperoxia-Induced Lung Injury in Preterm Rabbits
BACKGROUND: Invasive mechanical ventilation (IMV) has become one of the mainstays of therapy in NICUs worldwide, as a result of which premature babies with extremely low birth weight have been able to survive. Although lifesaving, IMV can result in lung inflammation and injury. Surfactant therapy is...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160647/ https://www.ncbi.nlm.nih.gov/pubmed/32327998 http://dx.doi.org/10.3389/fphys.2020.00266 |
_version_ | 1783522797089193984 |
---|---|
author | Das, Pragnya Curstedt, Tore Agarwal, Beamon Prahaladan, Varsha M. Ramirez, John Bhandari, Shreya Syed, Mansoor A. Salomone, Fabrizio Casiraghi, Costanza Pelizzi, Nicola Bhandari, Vineet |
author_facet | Das, Pragnya Curstedt, Tore Agarwal, Beamon Prahaladan, Varsha M. Ramirez, John Bhandari, Shreya Syed, Mansoor A. Salomone, Fabrizio Casiraghi, Costanza Pelizzi, Nicola Bhandari, Vineet |
author_sort | Das, Pragnya |
collection | PubMed |
description | BACKGROUND: Invasive mechanical ventilation (IMV) has become one of the mainstays of therapy in NICUs worldwide, as a result of which premature babies with extremely low birth weight have been able to survive. Although lifesaving, IMV can result in lung inflammation and injury. Surfactant therapy is considered a standard of care in preterm infants with immature lungs. Recently, small molecule inhibitors like siRNAs and miRNAs have been used for therapeutic purposes. Ddit3 (CHOP), Ang2 and miR34a are known to be upregulated in experimental lung injury. We wanted to test whether inhibitors for these molecules (CHOP siRNA, Ang2 siRNA, and miR34a antagomir) if used alone or with a combination with surfactant (Curosurf(®)) would help in reducing ventilation and hyperoxia-induced injury in an experimental lung injury model. METHODS: Preterm rabbits born by cesarean section were intratracheally instilled with the three small molecule inhibitors with or without Curosurf(®) prior to IMV and hyperoxia exposure. Prior to testing the inhibitors in rabbits, these small molecule inhibitors were transfected in mouse lung epithelial cells (MLE12 and AECII) and delivered to neonatal mouse pups intranasally as a proof of concept that surfactant (Curosurf(®)) could be used as an effective vehicle for administration of such drugs. Survival, pulmonary function tests, histopathology, immunostaining, quantitative PCR and western blotting were done to see the adjuvant effect of surfactant with these three small molecule inhibitors. RESULTS: Our data shows that Curosurf(®) can facilitate transfection of small molecules in MLE12 cells with the same and/or increased efficiency as Lipofectamine. Surfactant given alone or as an adjuvant with small molecule inhibitors increases survival, decreases IMV and hyperoxia-induced inflammation, improves pulmonary function and lung injury scores in preterm rabbit kits. CONCLUSION: Our study shows that Curosurf(®) can be used successfully as an adjuvant therapy with small molecule inhibitors for CHOP/Ang2/miR34a. In this study, of the three inhibitors used, miR34a inhibitor seemed to be the most promising compound to combat IMV and hyperoxia-induced lung injury in preterm rabbits. |
format | Online Article Text |
id | pubmed-7160647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71606472020-04-23 Small Molecule Inhibitor Adjuvant Surfactant Therapy Attenuates Ventilator- and Hyperoxia-Induced Lung Injury in Preterm Rabbits Das, Pragnya Curstedt, Tore Agarwal, Beamon Prahaladan, Varsha M. Ramirez, John Bhandari, Shreya Syed, Mansoor A. Salomone, Fabrizio Casiraghi, Costanza Pelizzi, Nicola Bhandari, Vineet Front Physiol Physiology BACKGROUND: Invasive mechanical ventilation (IMV) has become one of the mainstays of therapy in NICUs worldwide, as a result of which premature babies with extremely low birth weight have been able to survive. Although lifesaving, IMV can result in lung inflammation and injury. Surfactant therapy is considered a standard of care in preterm infants with immature lungs. Recently, small molecule inhibitors like siRNAs and miRNAs have been used for therapeutic purposes. Ddit3 (CHOP), Ang2 and miR34a are known to be upregulated in experimental lung injury. We wanted to test whether inhibitors for these molecules (CHOP siRNA, Ang2 siRNA, and miR34a antagomir) if used alone or with a combination with surfactant (Curosurf(®)) would help in reducing ventilation and hyperoxia-induced injury in an experimental lung injury model. METHODS: Preterm rabbits born by cesarean section were intratracheally instilled with the three small molecule inhibitors with or without Curosurf(®) prior to IMV and hyperoxia exposure. Prior to testing the inhibitors in rabbits, these small molecule inhibitors were transfected in mouse lung epithelial cells (MLE12 and AECII) and delivered to neonatal mouse pups intranasally as a proof of concept that surfactant (Curosurf(®)) could be used as an effective vehicle for administration of such drugs. Survival, pulmonary function tests, histopathology, immunostaining, quantitative PCR and western blotting were done to see the adjuvant effect of surfactant with these three small molecule inhibitors. RESULTS: Our data shows that Curosurf(®) can facilitate transfection of small molecules in MLE12 cells with the same and/or increased efficiency as Lipofectamine. Surfactant given alone or as an adjuvant with small molecule inhibitors increases survival, decreases IMV and hyperoxia-induced inflammation, improves pulmonary function and lung injury scores in preterm rabbit kits. CONCLUSION: Our study shows that Curosurf(®) can be used successfully as an adjuvant therapy with small molecule inhibitors for CHOP/Ang2/miR34a. In this study, of the three inhibitors used, miR34a inhibitor seemed to be the most promising compound to combat IMV and hyperoxia-induced lung injury in preterm rabbits. Frontiers Media S.A. 2020-04-09 /pmc/articles/PMC7160647/ /pubmed/32327998 http://dx.doi.org/10.3389/fphys.2020.00266 Text en Copyright © 2020 Das, Curstedt, Agarwal, Prahaladan, Ramirez, Bhandari, Syed, Salomone, Casiraghi, Pelizzi and Bhandari. http://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 | Physiology Das, Pragnya Curstedt, Tore Agarwal, Beamon Prahaladan, Varsha M. Ramirez, John Bhandari, Shreya Syed, Mansoor A. Salomone, Fabrizio Casiraghi, Costanza Pelizzi, Nicola Bhandari, Vineet Small Molecule Inhibitor Adjuvant Surfactant Therapy Attenuates Ventilator- and Hyperoxia-Induced Lung Injury in Preterm Rabbits |
title | Small Molecule Inhibitor Adjuvant Surfactant Therapy Attenuates Ventilator- and Hyperoxia-Induced Lung Injury in Preterm Rabbits |
title_full | Small Molecule Inhibitor Adjuvant Surfactant Therapy Attenuates Ventilator- and Hyperoxia-Induced Lung Injury in Preterm Rabbits |
title_fullStr | Small Molecule Inhibitor Adjuvant Surfactant Therapy Attenuates Ventilator- and Hyperoxia-Induced Lung Injury in Preterm Rabbits |
title_full_unstemmed | Small Molecule Inhibitor Adjuvant Surfactant Therapy Attenuates Ventilator- and Hyperoxia-Induced Lung Injury in Preterm Rabbits |
title_short | Small Molecule Inhibitor Adjuvant Surfactant Therapy Attenuates Ventilator- and Hyperoxia-Induced Lung Injury in Preterm Rabbits |
title_sort | small molecule inhibitor adjuvant surfactant therapy attenuates ventilator- and hyperoxia-induced lung injury in preterm rabbits |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160647/ https://www.ncbi.nlm.nih.gov/pubmed/32327998 http://dx.doi.org/10.3389/fphys.2020.00266 |
work_keys_str_mv | AT daspragnya smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits AT curstedttore smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits AT agarwalbeamon smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits AT prahaladanvarsham smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits AT ramirezjohn smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits AT bhandarishreya smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits AT syedmansoora smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits AT salomonefabrizio smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits AT casiraghicostanza smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits AT pelizzinicola smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits AT bhandarivineet smallmoleculeinhibitoradjuvantsurfactanttherapyattenuatesventilatorandhyperoxiainducedlunginjuryinpretermrabbits |