Zhang Chi, Paddock Kieran, Chou Adriana, Scholp Austin, Gong Ting, Jiang Jack J
Department of Otolaryngology-Head and Neck Surgery, Eye, Ear, Nose, and Throat Hospital of Fudan University, 83 Fenyang Road, Shanghai, 200031, China.
Division of Otolaryngology-Head and Neck Surgery, Department of Surgery, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, 53792, USA.
Eur Arch Otorhinolaryngol. 2018 Jun;275(6):1547-1556. doi: 10.1007/s00405-018-4973-9. Epub 2018 Apr 18.
Voice abuse is known to be a common risk factor of voice disorders and prolonged; high-intensity phonation has been shown to damage the vocal fold epithelium. We aim to evaluate the effects of phonation on the integrity and barrier function of vocal fold epithelium using a porcine laryngeal model.
Ex vivo porcine larynges were phonated at low intensity or high intensity for 15, 30, or 60 min within 4 h after harvest. Vocal fold epithelium was visualized using transmission electron microscopy (TEM). The barrier function of vocal fold epithelium was evaluated by measuring the permeability to model molecules, fluorescein (376 Da), and fluorescein isothiocyanate (FITC)-dextrans of 4000 and 10,000 Da (FD4, FD10), in a Franz diffusing cell.
Cell death and dilated intercellular space after phonation were observed using TEM. Thickness of vocal fold epithelium was significantly reduced after low-intensity phonation for 30 and 60 min and high-intensity phonation for 15, 30, and 60 min. Epithelial permeability to fluorescein was significantly increased after low-intensity phonation for 30 and 60 min, and high-intensity phonation. Permeability to FD4 was significantly increased after high-intensity phonation for 30 and 60 min. Phonation did not alter the permeability to FD10 significantly.
Long-duration phonation destroys the integrity and barrier function of vocal fold epithelium. These effects likely make vocal folds more vulnerable to other environmental irritants, such as tobacco smoke, reflux components, allergens, and inhaled pollutants. Destroyed barrier function may be an important factor in the pathogenesis of voice lesions related to voice abuse.
嗓音滥用是已知的嗓音障碍常见危险因素,长期高强度发声已被证明会损害声带上皮。我们旨在使用猪喉模型评估发声对声带上皮完整性和屏障功能的影响。
离体猪喉在收获后4小时内分别以低强度或高强度发声15、30或60分钟。使用透射电子显微镜(TEM)观察声带上皮。通过在Franz扩散池中测量对模型分子、荧光素(376Da)以及4000和10000Da的异硫氰酸荧光素(FITC)-葡聚糖(FD4、FD10)的通透性来评估声带上皮的屏障功能。
使用TEM观察到发声后细胞死亡和细胞间间隙增宽。低强度发声30和60分钟以及高强度发声15、30和60分钟后,声带上皮厚度显著降低。低强度发声30和60分钟以及高强度发声后,上皮对荧光素的通透性显著增加。高强度发声30和60分钟后,对FD4的通透性显著增加。发声对FD10的通透性没有显著改变。
长时间发声会破坏声带上皮的完整性和屏障功能。这些影响可能使声带更容易受到其他环境刺激物的影响,如烟草烟雾、反流成分、过敏原和吸入污染物。受损的屏障功能可能是与嗓音滥用相关的嗓音病变发病机制中的一个重要因素。