## Objectives: Vocal fold injury can be irreversible, leading to vocal fold scarring, with permanent functional effects and no optimal treatment. a porcine model of vocal fold scarring was used to test effects of decorin and primed vocal fold fibroblasts in vitro using a cell migration assay and im
In vivo and in vitro models of ionizing radiation to the vocal folds
β Scribed by Benjamin Saltman; Dennis H. Kraus; Hazel Szeto; Bhupesh Parashar; Ronald Ghossein; Diane Felsen; Ryan C. Branski
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 363 KB
- Volume
- 32
- Category
- Article
- ISSN
- 1043-3074
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Background
Radiation therapy (RT) to the head and neck often results in damage to the vocal folds (VF) and surrounding structures. Characterization and treatment of these sequelae is limited, likely due to the lack of experimental models.
Methods
Larynges from rats exposed to 2 fractionation schedules (40 Gy total) were analyzed histologically. In vitro, reactive oxygen species (ROS) synthesis, and transcription of select genes associated with ROS, inflammation, and fibrosis were examined in VF fibroblasts after singleβdose radiation.
Results
Although radiationβinduced histologic alterations are made to VF architecture, 1 fractionation schedule was accompanied by significant morbidity and mortality. In vitro, radiation increased ROS synthesis and inflammatory and profibrotic gene expression.
Conclusion
Our data suggest that hyperfractionated RT is more tolerable. Utilizing this model, RTβinduced histologic aberrations are made to the VF mucosa. In addition, a relationship between radiation, ROS, and inflammatory and fibrotic gene expression was observed in vitro. Β© 2009 Wiley Periodicals, Inc. Head Neck, 2010
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