Kimball Emily E, Sayce Lea, Powell Maria, Gartling Gary J, Brandley Jennifer, Rousseau Bernard
Department of Hearing and Speech Sciences, Vanderbilt University, Nashville, Tennessee.
Department of Communication Science and Disorders, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Otolaryngology, Vanderbilt University Medical Center, Nashville, Tennessee.
J Voice. 2021 Mar;35(2):216-225. doi: 10.1016/j.jvoice.2019.08.023. Epub 2019 Sep 18.
Vibration of the vocal folds can disrupt the tissue and induce structural, functional, and molecular changes; the presence or absence of contact between the vocal folds during vibration can affect the type and extent of these changes. The purpose of this study was to characterize vocal fold changes following 2 hours of contact phonation or phonation without vibratory contact.
Six New Zealand white breeder rabbits underwent 120 minutes of phonation with or without vibratory contact, and four served as nonphonated controls. The larynx was exposed and current was applied to the cricothyroids bilaterally to achieve vocal fold adduction while humidified airflow was delivered to induce vocal fold vibration. Laryngeal position, airflow, and stimulation levels were adjusted to obtain phonation with or without contact, and phonation was elicited for 120 minutes. Following excision, larynges were stained using Hematoxylin & Eosin, Elastica van Gieson, and Grocott's Methenamine Silver, or labeled with immunofluorescent markers for E-cadherin, CD31, CD11b, and Vimentin. All images were captured using a Nikon 90i microscope and analyzed using ImageJ.
Differences between vibratory conditions and control samples were observed. There was more extensive epithelial thinning, reduced epithelial integrity and increased vascularity in the contact phonation group, while both phonatory groups demonstrated a decreased presence of mucous on the luminal surface and a decrease in elastin band thickness and lamina propria depth. Neither condition showed differences in inflammatory cell presence compared to control tissue.
By showing that these two vibratory conditions result in structural changes of different types and magnitude, we have provided the first empirical evidence that vocal fold tissue is sensitive to differences in forces, and that changes in vibratory pattern can elicit different downstream biological changes within the tissue. The differences described herein are an important step toward understanding the vocal folds' potential for differential response to phonotraumatic damage following different vibratory behaviors.
声带振动会破坏组织并引发结构、功能和分子变化;振动过程中声带之间是否接触会影响这些变化的类型和程度。本研究的目的是描述在2小时的接触发声或无振动接触发声后声带的变化。
六只新西兰白色种兔进行120分钟的有或无振动接触的发声,四只作为未发声对照。暴露喉部,双侧向环甲肌施加电流以实现声带内收,同时输送加湿气流以诱导声带振动。调整喉部位置、气流和刺激水平以获得有或无接触的发声,并诱发发声120分钟。切除后,喉部用苏木精和伊红、弹性纤维染色液和Grocott六胺银染色,或用E-钙黏蛋白、CD31、CD11b和波形蛋白的免疫荧光标记物标记。所有图像均使用尼康90i显微镜拍摄并用ImageJ分析。
观察到振动条件与对照样本之间存在差异。接触发声组出现更广泛的上皮变薄、上皮完整性降低和血管增多,而两个发声组均显示管腔表面黏液减少以及弹性蛋白带厚度和固有层深度减小。与对照组织相比,两种情况在炎症细胞存在方面均未显示差异。
通过表明这两种振动条件会导致不同类型和程度的结构变化,我们提供了首个实证证据,即声带组织对力的差异敏感,并且振动模式的变化可在组织内引发不同的下游生物学变化。本文所述的差异是朝着理解声带在不同振动行为后对发声创伤性损伤的不同反应潜力迈出的重要一步。