Biochemical and histopathological evaluation of systemic and ocular toxicity of favipiravir in rats.

Autor: Özcan D; Department of Ophthalmology, University of Health Sciences, Seyrantepe Hamidiye Etfal Training and Research Hospital, İstanbul, Turkey., Özçelik F; Department of Medical Biochemistry, University of Health Sciences, Seyrantepe Hamidiye Etfal Training and Research Hospital, İstanbul, Turkey., Mammadov R; Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey., Aktaş M; Department of Biochemistry, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey., Altındağ F; Department of Histology and Embryology, Faculty of Medicine, Van Yüzüncü Yıl University, Van, Turkey., Alkan AA; Department of Ophthalmology, İstanbul Cerrahi Hospital, İstanbul, Turkey., Karapapak M; Department of Ophthalmology, Başakşehir Çam and Sakura City Hospital, İstanbul, Turkey., Altuner D; Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey., Süleyman H; Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey.
Jazyk: angličtina
Zdroj: Cutaneous and ocular toxicology [Cutan Ocul Toxicol] 2024 Jun; Vol. 43 (2), pp. 105-112. Date of Electronic Publication: 2024 Jan 12.
DOI: 10.1080/15569527.2023.2300788
Abstrakt: Purpose: Favipiravir (FAV) used against COVID-19 is an antiviral drug that causes adverse reactions, such as hyperuricaemia, liver damage, and hematopoetic toxicity. The aim of the study was to investigate the systemic and ocular side-effects of FAV in rats, for the first time. Materials and methods: A total of 18 albino male Wistar rats were used in the study. The rats were divided into 3 groups as the healthy group (HG), the group given 50 mg/kg/day favipiravir (FAV50), and the group given 200 mg/kg/d favipiravir (FAV200). These doses were given to the experimental groups for one week. At the end of the experiment histopathological examinations were performed on the conjunctiva and sclera of the eye. In addition, malondialdehyde (MDA), total glutathione (tGSH), superoxide dismutase (SOD), interleukin-1β (IL-1β), and tumor necrosis factor alpha (TNF-α) levels were measured in blood samples taken from rats. Results: Compared to HG, the MDA (1.37 ± 0.61 vs. 4.82 ± 1.40 µmol/mL), IL-1β (2.52 ± 1.14 vs . 6.67 ± 1.99 pg/mL), and TNF-α levels (3.28 ± 1.42 vs . 8.53 ± 3.06 pg/mL) of the FAV200 group were higher. The levels of tGSH (7.58 ± 1.98 vs. 2.50 ± 0.98 nmol/mL) and SOD (13.63 ± 3.43 vs . 3.81 ± 1.43 U/mL) the FAV200 group were lower than the HG ( p  < 0.05, for all). The degree of damage to the cornea and sclera of the FAV200 group was quite high according to HG ( p  < 0.001). Conclusions: FAV can cause damage to rat conjunctiva and sclera by increasing oxidant stress and inflammation at high dose.
Databáze: MEDLINE