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.2022 Sep 5;14(9):e28796.
doi: 10.7759/cureus.28796. eCollection 2022 Sep.

Effects of Vitamin C on the Oral-Nasal Mucosal Damage Caused by Favipiravir in Old and Young Rats

Affiliations

Effects of Vitamin C on the Oral-Nasal Mucosal Damage Caused by Favipiravir in Old and Young Rats

Yücel Kurt et al. Cureus..

Abstract

Background Favipiravir was widely used to treat coronavirus disease 2019 (COVID-19) early in the pandemic. Later, many reports began to be published about the side effects of favipiravir on different tissues. However, the side effects of favipiravir on the oral and nasal mucosa remain unknown. This experimental study aimed to evaluate the pathological effects of favipiravir on the oral-nasal mucosa and investigate whether vitamin C (Vit C) reduces these lesions in old and young rats. Methodology A total of 100 rats were used for this study. The rats were administered favipiravir (20 mg/kg and 100 mg/kg) and Vit C (150 mg/kg/day) for 14 days. At the end of the study, rats were euthanatized, and oral-nasal mucosal histopathological changes were evaluated. Nuclear factor kappa-ligand (RANKL) and caspase-3 expressions were immunohistochemically examined. Results Favipiravir caused severe lesions in old rats compared to young, and the severity of the lesions increased with the dosage. Severe hyperemia and erosive-ulcerative lesions were observed in the oral-nasal mucosa. In addition, increased RANKL and caspase-3 expressions were observed in a dose-dependent manner. In both young and old groups, Vit C treatment showed decreased caspase-3 and RANKL expression; a more prominent decrease was seen in young rats. Conclusions This study showed that favipiravir could cause histopathological lesions in the oral and nasal mucosa. However, the administration of Vit C with favipiravir can provide a protective effect against this damage. The curative effect of Vit C was more pronounced in young rats and at low doses.

Keywords: caspase-3; covid-19; favipiravir; oral-nasal mucosa; pathology; rankl; vitamin c.

Copyright © 2022, Kurt et al.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Groups and treatments for groups.
Favi: favipiravir; Vit C: vitamin C
Figure 2
Figure 2. Histopathological appearance of the oral mucosa between the groups.
Arrowheads indicate shedding of the keratin layer; thick arrows indicate erosive ulcerative lesions; thin arrows indicate inflammatory cell infiltrations. H&E, scale bars = 50 µm. Favi: favipiravir; Vit C: vitamin C; H&E: hematoxylin and eosin
Figure 3
Figure 3. Histopathological appearance of the nasal mucosa between the groups.
Thick arrows indicate erosive ulcerative lesions; thin arrows indicate inflammatory cell infiltrations. H&E, scale bars = 50 µm. Favi: favipiravir; Vit C: vitamin C; H&E: hematoxylin and eosin
Figure 4
Figure 4. Caspase-3 expressions in oral mucosa between the groups.
Arrows indicate positive cells: streptavidin-biotin peroxidase method. Scale bars = 50 µm. Favi: favipiravir; Vit C: vitamin C
Figure 5
Figure 5. Caspase-3 expressions in the nasal mucosa among the groups.
Arrows indicate positive cells: streptavidin-biotin peroxidase method. Scale bars = 50 µm. Favi: favipiravir; Vit C: vitamin C
Figure 6
Figure 6. RANKL expressions in the oral mucosa between the groups.
Arrows indicate positive cells: streptavidin-biotin peroxidase method. Scale bars = 50 µm. Favi: favipiravir; Vit C: vitamin C
Figure 7
Figure 7. RANKL expressions in the nasal mucosa between the groups.
Arrows indicate positive cells: streptavidin-biotin peroxidase method. Scale bars = 50 µm. Favi: favipiravir; Vit C: vitamin C
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References

    1. Clinical characteristics of coronavirus disease 2019 in China. Guan WJ, Ni ZY, Hu Y, et al. N Engl J Med. 2020;382:1708–1720. - PMC - PubMed
    1. Review of the 2019 novel coronavirus (SARS-CoV-2) based on current evidence. Wang L, Wang Y, Ye D, Liu Q. Int J Antimicrob Agents. 2020;55:105948. - PMC - PubMed
    1. Diagnostic and early prognostic value of serum CRP and LDH levels in patients with possible COVID-19 at the first admission. Akdogan D, Guzel M, Tosun D, Akpinar O. J Infect Dev Ctries. 2021;15:766–772. - PubMed
    1. Pharmacologic treatments for coronavirus disease 2019 (COVID-19): a review. Sanders JM, Monogue ML, Jodlowski TZ, Cutrell JB. JAMA. 2020;323:1824–1836. - PubMed
    1. Experimental treatment with favipiravir for COVID-19: an open-label control study. Cai Q, Yang M, Liu D, et al. Engineering (Beijing) 2020;6:1192–1198. - PMC - PubMed

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