Park Jisu, Kim Bo-Young, Park Eun Jung, Shin Yong-Il, Ryu Ji Hyeon
Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Gyeongnam, Republic of Korea.
Department of Rehabilitation Medicine, School of Medicine, Pusan National University, Yangsan 50612, Gyeongnam, Republic of Korea.
Antioxidants (Basel). 2024 Aug 19;13(8):1003. doi: 10.3390/antiox13081003.
Exposure to particulate matter (PM), especially PM, 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 exposure. The mice received sensitization with ovalbumin (OVA) and were subsequently treated with PM 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 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-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. These findings suggest that PBM could be a promising intervention for PM-induced respiratory complications in patients with allergic asthma.
已知接触颗粒物(PM),尤其是细颗粒物,会加重哮喘,构成重大的公共卫生风险。本研究在模拟因接触PM而加剧的过敏性气道炎症的小鼠模型中,研究了光生物调节(PBM)对哮喘的缓解作用。小鼠用卵清蛋白(OVA)致敏,随后在激发过程中每3天以0.1mg/kg的剂量给予PM,持续3周,共9次。使用610nm波长的发光二极管,以1.7mW/cm²的功率通过直接皮肤接触对呼吸道进行PBM治疗,每天20分钟,持续19天。结果表明,PBM显著降低了暴露于PM的哮喘小鼠的气道高反应性、血浆免疫球蛋白E(IgE)和OVA特异性IgE、气道炎症、2型辅助性T细胞细胞因子、支气管肺泡灌洗液(BALF)中的组胺和类胰蛋白酶,以及杯状细胞增生。此外,PBM通过减少胶原蛋白沉积、气道平滑肌质量和纤维化相关基因的表达,减轻了上皮下纤维化。它减轻了暴露于PM的哮喘小鼠的活性氧生成、氧化应激、内质网应激、凋亡性细胞死亡、铁死亡,并调节了自噬信号。这些发现表明,PBM可能是治疗过敏性哮喘患者PM诱导的呼吸道并发症的一种有前景的干预措施。