Protective effects of resveratrol against fumonisin B1-induced liver toxicity in mice

The aim of this study was to investigate the effects of resveratrol against fumonisin B1 (FB1)-induced liver toxicity, as, to the best of our knowledge, these effects have not been investigated yet, even though the toxic effects and mechanisms of FB1 and the antioxidative effects of resveratrol are...

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Main Authors: Yalçın Rıza, Kart Asım, Özmen Özlem, Zeybek Esra
Format: Article
Language:English
Published: Sciendo 2023-06-01
Series:Arhiv za Higijenu Rada i Toksikologiju
Subjects:
Online Access:https://doi.org/10.2478/aiht-2023-74-3648
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author Yalçın Rıza
Kart Asım
Özmen Özlem
Zeybek Esra
author_facet Yalçın Rıza
Kart Asım
Özmen Özlem
Zeybek Esra
author_sort Yalçın Rıza
collection DOAJ
description The aim of this study was to investigate the effects of resveratrol against fumonisin B1 (FB1)-induced liver toxicity, as, to the best of our knowledge, these effects have not been investigated yet, even though the toxic effects and mechanisms of FB1 and the antioxidative effects of resveratrol are well known. 40 BALB/c mice were divided into control, FB1, resveratrol, and FB1+resveratrol groups. Control received saline for 14 days. The FB1 group received 2.25 mg/kg FB1 every other day for 14 days. The resveratrol group received 10 mg/kg resveratrol for 14 days. The FB1+resveratrol group received 2.25 mg/kg FB1 every other day and 10 mg/kg resveratrol every day for 14 days. All administrations were peritoneal. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), total sialic acid (TSA) levels were analysed in serum samples, while total antioxidant status (TAS) and total oxidant status (TOS) were measured in the liver. Additionally, the liver tissue was examined for histopathological changes. AST, ALT, and TSA were significantly higher in the FB1 group than control. Resveratrol countered FB1 effects for all parameters, including TOS and TAS. Liver histology showed FB1-induced hyperaemia, infiltrations, and megalokaryosis in some hepatocytes. No pathological findings were detected in the control, resveratrol, or FB1+resveratrol group. Our findings confirm resveratrol’s protective effect against liver damage and oxidative stress caused by FB1. In addition, they suggest that increased serum TSA levels can be used as a biomarker of FB1-induced hepatotoxicity.
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spelling doaj.art-9c9d366d2103480fa8acf6eae7d0b2832023-09-04T07:10:48ZengSciendoArhiv za Higijenu Rada i Toksikologiju1848-63122023-06-0174211511910.2478/aiht-2023-74-3648Protective effects of resveratrol against fumonisin B1-induced liver toxicity in miceYalçın Rıza0Kart Asım1Özmen Özlem2Zeybek Esra31Burdur Mehmet Akif Ersoy University, Faculty of Veterinary Medicine, Department of Pharmacology and Toxicology, Burdur, Turkey1Burdur Mehmet Akif Ersoy University, Faculty of Veterinary Medicine, Department of Pharmacology and Toxicology, Burdur, Turkey2Burdur Mehmet Akif Ersoy University, Faculty of Veterinary Medicine, Department of Pathology, Burdur, Turkey1Burdur Mehmet Akif Ersoy University, Faculty of Veterinary Medicine, Department of Pharmacology and Toxicology, Burdur, TurkeyThe aim of this study was to investigate the effects of resveratrol against fumonisin B1 (FB1)-induced liver toxicity, as, to the best of our knowledge, these effects have not been investigated yet, even though the toxic effects and mechanisms of FB1 and the antioxidative effects of resveratrol are well known. 40 BALB/c mice were divided into control, FB1, resveratrol, and FB1+resveratrol groups. Control received saline for 14 days. The FB1 group received 2.25 mg/kg FB1 every other day for 14 days. The resveratrol group received 10 mg/kg resveratrol for 14 days. The FB1+resveratrol group received 2.25 mg/kg FB1 every other day and 10 mg/kg resveratrol every day for 14 days. All administrations were peritoneal. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), total sialic acid (TSA) levels were analysed in serum samples, while total antioxidant status (TAS) and total oxidant status (TOS) were measured in the liver. Additionally, the liver tissue was examined for histopathological changes. AST, ALT, and TSA were significantly higher in the FB1 group than control. Resveratrol countered FB1 effects for all parameters, including TOS and TAS. Liver histology showed FB1-induced hyperaemia, infiltrations, and megalokaryosis in some hepatocytes. No pathological findings were detected in the control, resveratrol, or FB1+resveratrol group. Our findings confirm resveratrol’s protective effect against liver damage and oxidative stress caused by FB1. In addition, they suggest that increased serum TSA levels can be used as a biomarker of FB1-induced hepatotoxicity.https://doi.org/10.2478/aiht-2023-74-3648altastliver damageoxidative stresstotal antioxidant statustotal oxidant statustotal sialic acidaltastoksidacijski stresoštećenje jetreukupni antioksidacijski statusukupni oksidacijski statusukupna sijalinska kiselina
spellingShingle Yalçın Rıza
Kart Asım
Özmen Özlem
Zeybek Esra
Protective effects of resveratrol against fumonisin B1-induced liver toxicity in mice
Arhiv za Higijenu Rada i Toksikologiju
alt
ast
liver damage
oxidative stress
total antioxidant status
total oxidant status
total sialic acid
alt
ast
oksidacijski stres
oštećenje jetre
ukupni antioksidacijski status
ukupni oksidacijski status
ukupna sijalinska kiselina
title Protective effects of resveratrol against fumonisin B1-induced liver toxicity in mice
title_full Protective effects of resveratrol against fumonisin B1-induced liver toxicity in mice
title_fullStr Protective effects of resveratrol against fumonisin B1-induced liver toxicity in mice
title_full_unstemmed Protective effects of resveratrol against fumonisin B1-induced liver toxicity in mice
title_short Protective effects of resveratrol against fumonisin B1-induced liver toxicity in mice
title_sort protective effects of resveratrol against fumonisin b1 induced liver toxicity in mice
topic alt
ast
liver damage
oxidative stress
total antioxidant status
total oxidant status
total sialic acid
alt
ast
oksidacijski stres
oštećenje jetre
ukupni antioksidacijski status
ukupni oksidacijski status
ukupna sijalinska kiselina
url https://doi.org/10.2478/aiht-2023-74-3648
work_keys_str_mv AT yalcınrıza protectiveeffectsofresveratrolagainstfumonisinb1inducedlivertoxicityinmice
AT kartasım protectiveeffectsofresveratrolagainstfumonisinb1inducedlivertoxicityinmice
AT ozmenozlem protectiveeffectsofresveratrolagainstfumonisinb1inducedlivertoxicityinmice
AT zeybekesra protectiveeffectsofresveratrolagainstfumonisinb1inducedlivertoxicityinmice