Shalaby Reham A, Emmanuel Acquah, Nezhad Fatemeh Dehgan, Akter Kohinur, Salam S M Abdus, Yi Jawoon, Kim Sang Seong, Park Jihwan, Kwon Hyuk Sang, Lee Kyung Hwa, Kim Young Ro, Chung Euiheon
Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, South Korea.
AI Graduate School, Gwangju Institute of Science and Technology, Gwangju, South Korea.
Transl Stroke Res. 2025 May 13. doi: 10.1007/s12975-025-01343-3.
Ischemic stroke often leads to neurological deficits, including olfactory dysfunction, which can significantly diminish quality of life. Photobiomodulation (PBM) has emerged as a promising therapeutic strategy for enhancing post-stroke recovery, although the molecular mechanisms, particularly regarding gene expression change, are not yet fully understood. This study investigates the long-term effects of photothrombosis (PT) on olfactory function and the olfactory bulb (OB) microenvironment, with a focus on PBM's efficacy during both early and late phases. In a mouse OB PT stroke model, PBM therapy (808-nm laser, 40 J/cm fluence, 325 mW/cm, 2 min daily) was applied from day 2 to day 7 post-PT. Olfactory function was monitored from pre-stroke through day 28 using the buried food test (BFT), and MRI scans were performed on days 7 and 28 to assess tissue damage. RNA sequencing (RNA-seq) and reverse transcription quantitative PCR (RT-qPCR) were conducted on day 7 to evaluate gene expression changes, with additional RT-qPCR analyses performed on day 28. PBM significantly accelerated olfactory function recovery by day 14, with full recovery maintained through day 28. Despite functional recovery, MRI results indicated persistent infarction at 28 days. RNA-seq identified upregulation of neuroprotective genes, including Gpr39 and Or4m1, following PBM treatment, suggesting enhanced gene expression related to acute-phase recovery. However, the impact of PBM on gene expression and functional recovery appeared to wane in the later stages of recovery. These findings underscore PBM's potential to enhance early-stage recovery in ischemic stroke, though its benefits may be more limited in the chronic phase.
缺血性中风常导致神经功能缺损,包括嗅觉功能障碍,这会显著降低生活质量。光生物调节(PBM)已成为一种有前景的促进中风后恢复的治疗策略,尽管其分子机制,特别是关于基因表达变化的机制,尚未完全明确。本研究调查光血栓形成(PT)对嗅觉功能和嗅球(OB)微环境的长期影响,重点关注PBM在早期和晚期的疗效。在小鼠OB PT中风模型中,从PT后第2天至第7天进行PBM治疗(808纳米激光,能量密度40 J/cm,325 mW/cm,每天2分钟)。使用埋食试验(BFT)从卒中前到第28天监测嗅觉功能,并在第7天和第28天进行MRI扫描以评估组织损伤。在第7天进行RNA测序(RNA-seq)和逆转录定量PCR(RT-qPCR)以评估基因表达变化,并在第28天进行额外的RT-qPCR分析。PBM在第14天显著加速了嗅觉功能恢复,并在第28天保持完全恢复。尽管功能恢复,但MRI结果显示在第28天仍有持续性梗死。RNA-seq确定PBM治疗后神经保护基因(包括Gpr39和Or4m1)上调,表明与急性期恢复相关的基因表达增强。然而,PBM对基因表达和功能恢复的影响在恢复后期似乎减弱。这些发现强调了PBM在增强缺血性中风早期恢复方面的潜力,尽管其在慢性期的益处可能更有限。