Cargando…

Rat model of smoke inhalation-induced acute lung injury

BACKGROUND: Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a lethal disease with limited therapeutic options and an unacceptably high mortality rate. Understanding the complex pathophysiological processes involved in the development of ALI/ARDS is critical for developing novel...

Descripción completa

Detalles Bibliográficos
Autores principales: Leiphrakpam, Premila Devi, Weber, Hannah R, Ogun, Tobi, Buesing, Keely L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311342/
https://www.ncbi.nlm.nih.gov/pubmed/34301712
http://dx.doi.org/10.1136/bmjresp-2021-000879
_version_ 1783728940846678016
author Leiphrakpam, Premila Devi
Weber, Hannah R
Ogun, Tobi
Buesing, Keely L
author_facet Leiphrakpam, Premila Devi
Weber, Hannah R
Ogun, Tobi
Buesing, Keely L
author_sort Leiphrakpam, Premila Devi
collection PubMed
description BACKGROUND: Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a lethal disease with limited therapeutic options and an unacceptably high mortality rate. Understanding the complex pathophysiological processes involved in the development of ALI/ARDS is critical for developing novel therapeutic strategies. Smoke inhalation (SI) injury is the leading cause of morbidity and mortality in patients with burn-associated ALI/ARDS; however, to our knowledge few reliable, reproducible models are available for pure SI animal model to investigate therapeutic options for ALI/ARDS without the confounding variables introduced by cutaneous burn or other pathology. OBJECTIVE: To develop a small animal model of pure SI-induced ALI and to use this model for eventual testing of novel therapeutics for ALI. METHODS: Rats were exposed to smoke using a custom-made smoke generator. Peripheral oxygen saturation (SpO(2)), heart rate, arterial blood gas, and chest X-ray (CXR) were measured before and after SI. Wet/dry weight (W/D) ratio, lung injury score and immunohistochemical staining of cleaved caspase 3 were performed on harvested lung tissues of healthy and SI animals. RESULTS: The current study demonstrates the induction of ALI in rats after SI as reflected by a significant, sustained decrease in SpO(2) and the development of diffuse bilateral pulmonary infiltrates on CXR. Lung tissue of animals exposed to SI showed increased inflammation, oedema and apoptosis as reflected by the increase in W/D ratio, injury score and cleaved caspase 3 level of the harvested tissues compared with healthy animals. CONCLUSION: We have successfully developed a small animal model of pure SI-induced ALI. This model is offered to the scientific community as a reliable model of isolated pulmonary SI-induced injury without the confounding variables of cutaneous injury or other systemic pathology to be used for study of novel therapeutics or other investigation.
format Online
Article
Text
id pubmed-8311342
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-83113422021-08-13 Rat model of smoke inhalation-induced acute lung injury Leiphrakpam, Premila Devi Weber, Hannah R Ogun, Tobi Buesing, Keely L BMJ Open Respir Res Respiratory Research BACKGROUND: Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a lethal disease with limited therapeutic options and an unacceptably high mortality rate. Understanding the complex pathophysiological processes involved in the development of ALI/ARDS is critical for developing novel therapeutic strategies. Smoke inhalation (SI) injury is the leading cause of morbidity and mortality in patients with burn-associated ALI/ARDS; however, to our knowledge few reliable, reproducible models are available for pure SI animal model to investigate therapeutic options for ALI/ARDS without the confounding variables introduced by cutaneous burn or other pathology. OBJECTIVE: To develop a small animal model of pure SI-induced ALI and to use this model for eventual testing of novel therapeutics for ALI. METHODS: Rats were exposed to smoke using a custom-made smoke generator. Peripheral oxygen saturation (SpO(2)), heart rate, arterial blood gas, and chest X-ray (CXR) were measured before and after SI. Wet/dry weight (W/D) ratio, lung injury score and immunohistochemical staining of cleaved caspase 3 were performed on harvested lung tissues of healthy and SI animals. RESULTS: The current study demonstrates the induction of ALI in rats after SI as reflected by a significant, sustained decrease in SpO(2) and the development of diffuse bilateral pulmonary infiltrates on CXR. Lung tissue of animals exposed to SI showed increased inflammation, oedema and apoptosis as reflected by the increase in W/D ratio, injury score and cleaved caspase 3 level of the harvested tissues compared with healthy animals. CONCLUSION: We have successfully developed a small animal model of pure SI-induced ALI. This model is offered to the scientific community as a reliable model of isolated pulmonary SI-induced injury without the confounding variables of cutaneous injury or other systemic pathology to be used for study of novel therapeutics or other investigation. BMJ Publishing Group 2021-07-23 /pmc/articles/PMC8311342/ /pubmed/34301712 http://dx.doi.org/10.1136/bmjresp-2021-000879 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Respiratory Research
Leiphrakpam, Premila Devi
Weber, Hannah R
Ogun, Tobi
Buesing, Keely L
Rat model of smoke inhalation-induced acute lung injury
title Rat model of smoke inhalation-induced acute lung injury
title_full Rat model of smoke inhalation-induced acute lung injury
title_fullStr Rat model of smoke inhalation-induced acute lung injury
title_full_unstemmed Rat model of smoke inhalation-induced acute lung injury
title_short Rat model of smoke inhalation-induced acute lung injury
title_sort rat model of smoke inhalation-induced acute lung injury
topic Respiratory Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311342/
https://www.ncbi.nlm.nih.gov/pubmed/34301712
http://dx.doi.org/10.1136/bmjresp-2021-000879
work_keys_str_mv AT leiphrakpampremiladevi ratmodelofsmokeinhalationinducedacutelunginjury
AT weberhannahr ratmodelofsmokeinhalationinducedacutelunginjury
AT oguntobi ratmodelofsmokeinhalationinducedacutelunginjury
AT buesingkeelyl ratmodelofsmokeinhalationinducedacutelunginjury