Murillo-Cuesta Silvia, Rodríguez-de la Rosa Lourdes, Contreras Julio, Celaya Adelaida M, Camarero Guadalupe, Rivera Teresa, Varela-Nieto Isabel
Institute for Biomedical Research "Alberto Sols" (IIBM), Spanish National Research Council-Autonomous University of Madrid (CSIC-UAM) Madrid, Spain ; Centre for Biomedical Network Research (CIBER), Institute of Health Carlos III (ISCIII) Madrid, Spain ; Hospital La Paz Institute for Health Research (IdiPAZ) Madrid, Spain.
Institute for Biomedical Research "Alberto Sols" (IIBM), Spanish National Research Council-Autonomous University of Madrid (CSIC-UAM) Madrid, Spain ; Centre for Biomedical Network Research (CIBER), Institute of Health Carlos III (ISCIII) Madrid, Spain ; Veterinary Faculty, Complutense University of Madrid Madrid, Spain.
Front Aging Neurosci. 2015 Mar 20;7:32. doi: 10.3389/fnagi.2015.00032. eCollection 2015.
Excessive exposure to noise damages the principal cochlear structures leading to hearing impairment. Inflammatory and immune responses are central mechanisms in cochlear defensive response to noise but, if unregulated, they contribute to inner ear damage and hearing loss. Transforming growth factor β (TGF-β) is a key regulator of both responses and high levels of this factor have been associated with cochlear injury in hearing loss animal models. To evaluate the potential of targeting TGF-β as a therapeutic strategy for preventing or ameliorating noise-induced hearing loss (NIHL), we studied the auditory function, cochlear morphology, gene expression and oxidative stress markers in mice exposed to noise and treated with TGF-β1 peptidic inhibitors P17 and P144, just before or immediately after noise insult. Our results indicate that systemic administration of both peptides significantly improved both the evolution of hearing thresholds and the degenerative changes induced by noise-exposure in lateral wall structures. Moreover, treatments ameliorated the inflammatory state and redox balance. These therapeutic effects were dose-dependent and more effective if the TGF-β1 inhibitors were administered prior to inducing the injury. In conclusion, inhibition of TGF-β1 actions with antagonistic peptides represents a new, promising therapeutic strategy for the prevention and repair of noise-induced cochlear damage.
过度暴露于噪音会损害主要的耳蜗结构,导致听力障碍。炎症和免疫反应是耳蜗对噪音防御反应的核心机制,但如果不受调控,它们会导致内耳损伤和听力丧失。转化生长因子β(TGF-β)是这两种反应的关键调节因子,在听力损失动物模型中,该因子的高水平与耳蜗损伤有关。为了评估将靶向TGF-β作为预防或改善噪音性听力损失(NIHL)的治疗策略的潜力,我们研究了在噪音暴露之前或之后立即用TGF-β1肽类抑制剂P17和P144处理的噪音暴露小鼠的听觉功能、耳蜗形态、基因表达和氧化应激标志物。我们的结果表明,两种肽的全身给药均显著改善了听力阈值的变化以及噪音暴露引起的侧壁结构退行性变化。此外,治疗改善了炎症状态和氧化还原平衡。这些治疗效果呈剂量依赖性,如果在诱导损伤之前给予TGF-β1抑制剂则更有效。总之,用拮抗肽抑制TGF-β1的作用代表了一种预防和修复噪音性耳蜗损伤的新的、有前景的治疗策略。