Volume 87, Issue 4 pp. 266-270
OTOLARYNGOLOGY HEAD AND NECK SURGERY

Response of an ovine laryngeal injury model to a novel fibrosis inhibitor

Jacqueline Allen

Corresponding Author

Jacqueline Allen

Faculty of Medical and Health Science, Department of Surgery, The University of Auckland, Auckland, New Zealand

Correspondence

Dr Jacqueline Allen, Faculty of Medical and Health Science, Department of Surgery, The University of Auckland, PO Box 92019, Newmarket, Auckland 1010, New Zealand. Email: [email protected]

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First published: 23 November 2016
Citations: 4
J. Allen MBChB, FRACS (ORL HNS).
This study was presented at the COSM ALA meeting, 22-23 April 2015, Boston, MA, USA.

Abstract

Background

Vocal fold injury results in severe voice alteration that limits occupational function and social interaction. An ovine model of laryngeal injury has been developed, validated and utilized to examine laryngeal wound healing and the effect of a novel collagen inhibitor (halofuginone) on surgical wound healing. The study design includes basic research and animal model.

Methods

An ovine laryngeal model was utilized to study controlled vocal fold injury and healing. Twenty-five sheep were divided into five groups. Sheep underwent right vocal fold injury preceded or followed by administration of halofuginone orally, topically or intralesionally. Biopsies were taken at commencement, 1 month and larynges explanted at 3 months. Specimens were examined for elastin and collagen density and epithelial changes. Pearson correlation statistics and Student's t-tests were used to assess inter-relationships.

Results

All sheep tolerated halofuginone. One sheep death occurred in an untreated sheep. Vocal fold tissue demonstrated a predictable histological response to injury. Elastin was significantly reduced post-injury in the glottis. Halofuginone administered orally for 10 weeks prevented elastin loss and demonstrated a trend of reducing collagen density post-injury.

Conclusion

In an ovine laryngeal injury model, administration of a fibrosis inhibitor resulted in altered elastin and collagen deposition after injury in the glottis. Further investigation is warranted to examine whether these tissue changes affect vocal fold dynamics.

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