Gastroprotective effect of vanillic acid against ethanol-induced gastric injury in rats: involvement of the NF-κB signalling and anti-apoptosis role.
Autor: | Arabacı Tamer S; School of Medicine, Department of Physiology, Sakarya University, Korucuk Mah. Konuralp Bulvarı No: 81/1 Korucuk Kampüsü, Adapazarı Sakarya, 54100, Türkiye. sarabaci@sakarya.edu.tr., Eskiler GG; School of Medicine, Department of Medical Biology, Sakarya University, Sakarya, Türkiye., Ercan F; School of Medicine, Department of Histology and Embryology, Marmara University, İstanbul, Türkiye. |
---|---|
Jazyk: | angličtina |
Zdroj: | Molecular biology reports [Mol Biol Rep] 2024 Jun 14; Vol. 51 (1), pp. 744. Date of Electronic Publication: 2024 Jun 14. |
DOI: | 10.1007/s11033-024-09672-6 |
Abstrakt: | Background: Vanillic acid (VA; 4-hydroxy-3-methoxybenzoic acid) is a flavouring agent found in various natural sources such as olives, fruits, and green tea. While VA exhibits numerous pharmacological effects, its potential protective effects against gastric injury warrants further investigation. Therefore, the primary objective of this study is to elucidate investigate the gastroprotective properties of VA against ethanol-induced gastric injury. Methods and Results: Rats were orally administered either saline or VA at different doses (50, 100, and 200 mg/kg/day), with omeprazole (20 mg/kg) serving as a positive control, for fourteen consecutive days before ethanol administration. Blood and gastric tissue samples were collected one hour after ethanol administration for biochemical, molecular, and histological analyses. Pre-treatment with VA before ulcer induction alleviated both macroscopic and microscopic damage. It also increased antioxidant glutathione levels and decreased malondialdehyde and myeloperoxidase activity, along with reducing inflammatory markers such as tumour necrosis factor (TNF)-α, interleukin (IL)-6, and nuclear factor kappa B (NF-κB). Additionally, VA pre-treatment reversed the elevation of Bax mRNA expression and gastric caspase-3 levels induced by gastric damage. It also mitigated the reduction in Bcl-2 mRNA expression. Conclusion: These findings suggest that VA exerts protective effects against ethanol-induced gastric injury in rats. It achieves this by augmenting gastric antioxidant capacity and mitigating oxidative, inflammatory, and apoptotic damage. (© 2024. The Author(s), under exclusive licence to Springer Nature B.V.) |
Databáze: | MEDLINE |
Externí odkaz: |