The Effects of Ellagic Acid on Experimental Corrosive Esophageal Burn Injury

• Published in: Current Issues in Molecular Biology Vol. 46; no. 2; pp. 1579 - 1592
• Main Authors: Keşim, Dilek Aygün, Aşır, Fırat, Ayaz, Hayat, Korak, Tuğcan
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.02.2024
• Subjects: anti-inflammatory; antioxidant; Antioxidants; Burns and scalds; Care and treatment; Collagen; corrosive substance; Ellagic acid; Epidermal growth factor; NaOH; Wounds and injuries; NaOH; anti-inflammatory; antioxidant; corrosive substance; ellagic acid
• ISSN: 1467-3045; 1467-3037; 1467-3045
• DOI: 10.3390/cimb46020102

This study aimed to investigate the antioxidant effect of Ellagic acid (EA) on wound healing in sodium hydroxide (NaOH)-induced corrosive esophageal burn injury. The interaction networks and functional annotations were conducted using Cytoscape software. A total of 24 Wistar albino rats were divided into control, corrosive esophageal burn (CEB) and CEB + EA groups. Burn injury was created by 20% NaOH and 30 mg/kg EA was per oral administered to rats. At the end of the 28-day experimental period, Malondialdehyde (MDA) content was measured. Esophageal tissue samples were processed for histological staining. The EA-target interaction network was revealed to be involved in regulating crucial cellular mechanisms for burn wound healing, with epidermal growth factor (EGF) identified as a central mediator. An increase in animal weight in the CEB + EA group was observed in the EA-treated group after CEB injury. Burn injury increased MDA content, but EA treatment decreased its level after CEB injury. Stenosis index, collagen degeneration, inflammation, fibrosis and necrosis levels were increased after CEB injury. EA treatment improved histopathology in the CEB + EA group compared to the CEB group. The expression of EGF was decreased in the CEB group but upregulated in the EA-treated group, suggesting a potential involvement of EA in cellular processes and tissue regeneration. EA, through its antioxidative and tissue regenerative properties, significantly contributes to alleviating the adverse effects of CEB injury, promoting wound healing.