scholarly journals In vivo investigation of acidified pepsin exposure to porcine vocal fold epithelia

2015 ◽  
Vol 126 (1) ◽  
pp. E12-E17 ◽  
Author(s):  
Abigail Durkes ◽  
M. Preeti Sivasankar
Keyword(s):  
PLoS ONE ◽  
2020 ◽  
Vol 15 (7) ◽  
pp. e0236348
Author(s):  
Naila Cannes do Nascimento ◽  
Andrea P. dos Santos ◽  
M. Preeti Sivasankar ◽  
Abigail Cox
Keyword(s):  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ryosuke Nakamura ◽  
Nao Hiwatashi ◽  
Renjie Bing ◽  
Carina P. Doyle ◽  
Ryan C. Branski

AbstractVocal fold (VF) fibrosis is a major cause of intractable voice-related disability and reduced quality of life. Excision of fibrotic regions is suboptimal and associated with scar recurrence and/or further iatrogenic damage. Non-surgical interventions are limited, putatively related to limited insight regarding biochemical events underlying fibrosis, and downstream, the lack of therapeutic targets. YAP/TAZ integrates diverse cell signaling events and interacts with signaling pathways related to fibrosis, including the TGF-β/SMAD pathway. We investigated the expression of YAP/TAZ following vocal fold injury in vivo as well as the effects of TGF-β1 on YAP/TAZ activity in human vocal fold fibroblasts, fibroblast-myofibroblast transition, and TGF-β/SMAD signaling. Iatrogenic injury increased nuclear localization of YAP and TAZ in fibrotic rat vocal folds. In vitro, TGF-β1 activated YAP and TAZ in human VF fibroblasts, and inhibition of YAP/TAZ reversed TGF-β1-stimulated fibroplastic gene upregulation. Additionally, TGF-β1 induced localization of YAP and TAZ in close proximity to SMAD2/3, and nuclear accumulation of SMAD2/3 was inhibited by a YAP/TAZ inhibitor. Collectively, YAP and TAZ were synergistically activated with the TGF-β/SMAD pathway, and likely essential for the fibroplastic phenotypic shift in VF fibroblasts. Based on these data, YAP/TAZ may evolve as an attractive therapeutic target for VF fibrosis.


2017 ◽  
Vol 31 (4) ◽  
pp. 513.e15-513.e23 ◽  
Author(s):  
Andrew M. Vahabzadeh-Hagh ◽  
Zhaoyan Zhang ◽  
Dinesh K. Chhetri

2019 ◽  
Author(s):  
Vlasta Lungova ◽  
Susan Thibeault

Abstract Development of treatments for vocal dysphonia has been inhibited by lack of human vocal fold (VF) mucosa models because of difficulty in procuring VF epithelial cells, epithelial cells’ limited proliferative capacity and absence of cell lines. We report development of engineered VF mucosae from hiPSC, transfected via TALEN constructs for green fluorescent protein, that mimic development of VF epithelial cells in utero. Modulation of FGF signaling achieves stratified squamous epithelium from definitive and anterior foregut derived cultures. Robust culturing of these cells on collagen-fibroblast constructs produces three-dimensional models comparable to in vivo VF mucosa.


2019 ◽  
Vol 9 (15) ◽  
pp. 3002 ◽  
Author(s):  
Mohsen Motie-Shirazi ◽  
Matías Zañartu ◽  
Sean D. Peterson ◽  
Daryush D. Mehta ◽  
James B. Kobler ◽  
...  

Excessive vocal fold collision pressures during phonation are considered to play a primary role in the formation of benign vocal fold lesions, such as nodules. The ability to accurately and reliably acquire intraglottal pressure has the potential to provide unique insights into the pathophysiology of phonotrauma. Difficulties arise, however, in directly measuring vocal fold contact pressures due to physical intrusion from the sensor that may disrupt the contact mechanics, as well as difficulty in determining probe/sensor position relative to the contact location. These issues are quantified and addressed through the implementation of a novel approach for identifying the timing and location of vocal fold contact, and measuring intraglottal and vocal fold contact pressures via a pressure probe embedded in the wall of a hemi-laryngeal flow facility. The accuracy and sensitivity of the pressure measurements are validated against ground truth values. Application to in vivo approaches are assessed by acquiring intraglottal and VF contact pressures using a synthetic, self-oscillating vocal fold model in a hemi-laryngeal configuration, where the sensitivity of the measured intraglottal and vocal fold contact pressure relative to the sensor position is explored.


2010 ◽  
Vol 18 (14) ◽  
pp. 14644 ◽  
Author(s):  
Ki Hean Kim ◽  
James A. Burns ◽  
Jonathan J. Bernstein ◽  
Gopi N. Maguluri ◽  
B. Hyle Park ◽  
...  

Author(s):  
Zhipeng Lou ◽  
Junshi Wang ◽  
James J. Daniero ◽  
Haibo Dong ◽  
Jinxiang Xi

Abstract In this paper, a numerical approach combined with experiments is employed to characterize the airflow through the vocal cord. Rabbits are used to perform in vivo magnetic resonance imaging (MRI) experiments and the MRI scan data are directly imposed for the three-dimensional (3D) reconstruction of a 3D high-fidelity model. The vibration modes are observed via the in vivo high-speed videoendoscopy (HSVM) technique, and the time-dependent glottal height is evaluated dynamically for the validation of the 3D reconstruction model. 72 sets of rabbit in vivo high-speed recordings are evaluated to achieve the most common vibration mode. The reconstruction is mainly based on MRI data and the HSVM records are supporting and validate the 3D model. A sharp-interface immersed-boundary-method (IBM)-based compressible flow solver is employed to compute the airflow. The primary purpose of the computational effort is to characterize the influence of the vocal folds that applied to the airflow and the airflow-induced phonation. The vocal fold kinematics and the vibration modes are quantified and the vortex structures are analyzed under the influence of vocal folds. The results have shown significant effects of the vocal fold height on the vortex structure, vorticity and velocity. The reconstructed 3D model from this work helps to bring insight into further understanding of the rabbit phonation mechanism. The results provide potential improvement for diagnosis of human vocal fold dysfunction and phonation disorder.


Author(s):  
James S. Drechsel ◽  
Jacob B. Munger ◽  
Allyson A. Pulsipher ◽  
Scott L. Thomson

The human vocal folds are responsible for sound production during normal speech, and a study of their flow-induced vibrations can lead to improved prevention and treatment of voice disorders. However, studying the vocal folds in vivo or using excised larynges has several disadvantages. Therefore, alternatives exist using either synthetic (physical) and/or computational vocal fold models. In order to be physiologically relevant, the behavior and properties of these models must reasonably match those of the human vocal folds.


Author(s):  
Shinji Deguchi ◽  
Kazutaka Kawashima

Mechanical properties of the vocal folds (such as stiffness or viscoelastic properties) play an essential role in phonation. They affect not only voice quality but also onset threshold of vocal fold self-excited oscillation, a sound source of voice [1]. Many experimental data on the mechanical properties have been reported so far, in which in vitro [2] or in vivo measurement techniques [3] were employed. In vitro measurements give us detailed information on the mechanical properties, yet it would be required to consider possible loss of freshness of the specimen. Meanwhile, current in vivo measurement methods utilize a thin probe to deform the vocal fold tissue located at the back of the throat and hence need technical skills for the surveyor to successfully obtain its loading-deformation relationship.


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