Photobiomodulation Mitigates PM<sub>2.5</sub>-Exacerbated Pathologies in a Mouse Model of Allergic Asthma

Exposure to particulate matter (PM), especially PM<sub>2.5</sub>, is known to exacerbate asthma, posing a significant public health risk. This study investigated the asthma-reducing effects of photobiomodulation (PBM) in a mice model mimicking allergic airway inflammation exacerbated by...

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Published in:Antioxidants
Main Authors: Jisu Park, Bo-Young Kim, Eun Jung Park, Yong-Il Shin, Ji Hyeon Ryu
Format: Article
Language:English
Published: MDPI AG 2024-08-01
Subjects:
Online Access:https://www.mdpi.com/2076-3921/13/8/1003
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author Jisu Park
Bo-Young Kim
Eun Jung Park
Yong-Il Shin
Ji Hyeon Ryu
author_facet Jisu Park
Bo-Young Kim
Eun Jung Park
Yong-Il Shin
Ji Hyeon Ryu
author_sort Jisu Park
collection DOAJ
container_title Antioxidants
description Exposure to particulate matter (PM), especially PM<sub>2.5</sub>, is known to exacerbate asthma, posing a significant public health risk. This study investigated the asthma-reducing effects of photobiomodulation (PBM) in a mice model mimicking allergic airway inflammation exacerbated by PM<sub>2.5</sub> exposure. The mice received sensitization with ovalbumin (OVA) and were subsequently treated with PM<sub>2.5</sub> at a dose of 0.1 mg/kg every 3 days, for 9 times over 3 weeks during the challenge. PBM, using a 610 nm wavelength LED, was applied at 1.7 mW/cm<sup>2</sup> to the respiratory tract via direct skin contact for 20 min daily for 19 days. Results showed that PBM significantly reduced airway hyperresponsiveness, plasma immunoglobulin E (IgE) and OVA-specific IgE, airway inflammation, T-helper type 2 cytokine, histamine and tryptase in bronchoalveolar lavage fluid (BALF), and goblet cell hyperplasia in PM<sub>2.5</sub>-exposed asthmatic mice. Moreover, PBM alleviated subepithelial fibrosis by reducing collagen deposition, airway smooth muscle mass, and expression of fibrosis-related genes. It mitigated reactive oxygen species generation, oxidative stress, endoplasmic reticulum stress, apoptotic cell death, ferroptosis, and modulated autophagic signals in the asthmatic mice exposed to PM<sub>2.5</sub>. These findings suggest that PBM could be a promising intervention for PM<sub>2.5</sub>-induced respiratory complications in patients with allergic asthma.
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spelling doaj-art-c546ec00d8a9442aa2ee080e6bb2f1b62025-08-20T00:29:38ZengMDPI AGAntioxidants2076-39212024-08-01138100310.3390/antiox13081003Photobiomodulation Mitigates PM<sub>2.5</sub>-Exacerbated Pathologies in a Mouse Model of Allergic AsthmaJisu Park0Bo-Young Kim1Eun Jung Park2Yong-Il Shin3Ji Hyeon Ryu4Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Gyeongnam, Republic of KoreaResearch Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Gyeongnam, Republic of KoreaResearch Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Gyeongnam, Republic of KoreaResearch Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Gyeongnam, Republic of KoreaResearch Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Gyeongnam, Republic of KoreaExposure to particulate matter (PM), especially PM<sub>2.5</sub>, is known to exacerbate asthma, posing a significant public health risk. This study investigated the asthma-reducing effects of photobiomodulation (PBM) in a mice model mimicking allergic airway inflammation exacerbated by PM<sub>2.5</sub> exposure. The mice received sensitization with ovalbumin (OVA) and were subsequently treated with PM<sub>2.5</sub> at a dose of 0.1 mg/kg every 3 days, for 9 times over 3 weeks during the challenge. PBM, using a 610 nm wavelength LED, was applied at 1.7 mW/cm<sup>2</sup> to the respiratory tract via direct skin contact for 20 min daily for 19 days. Results showed that PBM significantly reduced airway hyperresponsiveness, plasma immunoglobulin E (IgE) and OVA-specific IgE, airway inflammation, T-helper type 2 cytokine, histamine and tryptase in bronchoalveolar lavage fluid (BALF), and goblet cell hyperplasia in PM<sub>2.5</sub>-exposed asthmatic mice. Moreover, PBM alleviated subepithelial fibrosis by reducing collagen deposition, airway smooth muscle mass, and expression of fibrosis-related genes. It mitigated reactive oxygen species generation, oxidative stress, endoplasmic reticulum stress, apoptotic cell death, ferroptosis, and modulated autophagic signals in the asthmatic mice exposed to PM<sub>2.5</sub>. These findings suggest that PBM could be a promising intervention for PM<sub>2.5</sub>-induced respiratory complications in patients with allergic asthma.https://www.mdpi.com/2076-3921/13/8/1003asthmaferroptosisoxidative stressparticulate matter (PM<sub>2.5</sub>)photobiomodulation
spellingShingle Jisu Park
Bo-Young Kim
Eun Jung Park
Yong-Il Shin
Ji Hyeon Ryu
Photobiomodulation Mitigates PM<sub>2.5</sub>-Exacerbated Pathologies in a Mouse Model of Allergic Asthma
asthma
ferroptosis
oxidative stress
particulate matter (PM<sub>2.5</sub>)
photobiomodulation
title Photobiomodulation Mitigates PM<sub>2.5</sub>-Exacerbated Pathologies in a Mouse Model of Allergic Asthma
title_full Photobiomodulation Mitigates PM<sub>2.5</sub>-Exacerbated Pathologies in a Mouse Model of Allergic Asthma
title_fullStr Photobiomodulation Mitigates PM<sub>2.5</sub>-Exacerbated Pathologies in a Mouse Model of Allergic Asthma
title_full_unstemmed Photobiomodulation Mitigates PM<sub>2.5</sub>-Exacerbated Pathologies in a Mouse Model of Allergic Asthma
title_short Photobiomodulation Mitigates PM<sub>2.5</sub>-Exacerbated Pathologies in a Mouse Model of Allergic Asthma
title_sort photobiomodulation mitigates pm sub 2 5 sub exacerbated pathologies in a mouse model of allergic asthma
topic asthma
ferroptosis
oxidative stress
particulate matter (PM<sub>2.5</sub>)
photobiomodulation
url https://www.mdpi.com/2076-3921/13/8/1003
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