Photobiomodulation Mitigates PM 2.5 -Exacerbated Pathologies in a Mouse Model of Allergic Asthma.
Jisu ParkBo-Young KimEun Jung ParkYong-Il ShinJi Hyeon RyuPublished in: Antioxidants (Basel, Switzerland) (2024)
Exposure to particulate matter (PM), especially PM 2.5 , 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 2.5 exposure. The mice received sensitization with ovalbumin (OVA) and were subsequently treated with PM 2.5 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 2 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 2.5 -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 2.5 . These findings suggest that PBM could be a promising intervention for PM 2.5 -induced respiratory complications in patients with allergic asthma.
Keyphrases
- particulate matter
- air pollution
- lung function
- cell death
- allergic rhinitis
- endoplasmic reticulum stress
- chronic obstructive pulmonary disease
- polycyclic aromatic hydrocarbons
- heavy metals
- smooth muscle
- oxidative stress
- high fat diet induced
- respiratory tract
- mouse model
- induced apoptosis
- reactive oxygen species
- randomized controlled trial
- diabetic rats
- emergency department
- type diabetes
- physical activity
- cystic fibrosis
- drinking water
- signaling pathway
- insulin resistance
- cell therapy
- ischemia reperfusion injury
- liver fibrosis
- single cell
- skeletal muscle
- single molecule
- anti inflammatory
- mass spectrometry
- atomic force microscopy