The Effects of Halofuginone on Wound Healing in the Rat Nasal Mucosa

Author:

Ceylan Seyit Mehmet1ORCID,Uysal Erdal2,Sokucu Mehmet3,Sezgin Efe4,Kanmaz Mahmut Alper1,Yurtseven Duygu Gok5,Bilal Nagihan6

Affiliation:

1. Department of Otorhinolaryngology, Faculty of Medicine, SANKO University, Gaziantep, Turkey

2. Department of General Surgery, Faculty of Medicine, SANKO University, Gaziantep, Turkey

3. Department of Pathology, Faculty of Medicine, SANKO University, Gaziantep, Turkey

4. Laboratory of Nutrigenomics and Epidemiology, Department of Food Engineering, Izmir Institute of Thechnology, Izmir, Turkey

5. Department of Histology and Embryology, Faculty of Medicine, SANKO University, Gaziantep, Turkey

6. Department of Otorhinolaryngology, Faculty of Medicine, Kahramanmaras Sutcu Imam University, Kahramanmaras, Turkey

Abstract

Background Halofuginone is an alkaloid febrifugine analogue and bioactive molecule that was isolated incidentally from the Dichroa febrifuga plant. The therapeutic efficacy of halofuginone in parasitic infections, scleroderma, inflammation, and fibrosis-related diseases, as well as in some types of cancer, has been previously reported. The effects of halofuginone on nasal mucosal damage are not yet known. Objective The aim of this study was to investigate the potential effect of topically applied halofuginone on wound healing in the mechanically injured nasal mucosa of rats. Methods A unilateral mucosal wound was created in the nasal cavity of 32 rats (aged 4 weeks) using the brushing technique. These rats were randomly divided into 4 groups. Although the control group did not receive an intervention, a dry pad, a saline-impregnated pad, or a pad impregnated with halofuginone were placed in the rats of the other 3 groups and left for 5 minutes. Rats were sacrificed on the 14th day, and a histological examination was performed. The nasal mucosa was assessed via hematoxylin-eosin and Masson’s trichrome staining. Results There were no statistically significant differences in epithelial thickness, inflammation, goblet cell formation, and epithelial disarray values between the halofuginone group and the control group ( P > .05). The subepithelial thickness was significantly decreased in the saline-treated group and the halofuginone-treated group ( P < .05), but a significantly lower level of subepithelial fibrosis was only observed in the halofuginone group compared to the other groups ( P < .05). Conclusions Topical halofuginone administration reduces the development of fibrosis and subepithelial edema after experimentally induced nasal mucosal injury, but it does not exert therapeutic or preventive effects on epithelial damage, inflammation, and goblet cell hyperplasia.

Publisher

SAGE Publications

Subject

General Medicine,Otorhinolaryngology,Immunology and Allergy

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