Al-Kut Hospital for Gynecology Obstetrics and Pediatrics, Ministry of Health, Baghdad, Iraq.
Department of Pharmacology and Toxicology, College of Pharmacy, University of Baghdad, Baghdad, Iraq.
J Med Life. 2023 May;16(5):712-718. doi: 10.25122/jml-2023-0052.
Intestinal mucositis (IM) is a common side effect of several anticancer medications, including 5-fluorouracil (5-FU), and can lead to treatment disruptions and compromised outcomes. IM has severe clinical effects such as diarrhea, erythematous mucosal lesions, and the development of ulcers accompanied by excruciating pain. This study aimed to evaluate the mucoprotective effects of ellagic acid on 5-FU-induced IM in mice. Mice were administered normal saline intraperitoneally for six days, followed by intraperitoneal injection of 5-FU for four days at a dose of 50 mg per kilogram. Ellagic acid was orally administered to the mice in groups III and IV in two doses (5 mg and 10 mg), with a one-hour time separation from 5-FU for ten days. At the end of the experiment, small intestine tissue was collected to measure the levels of antioxidant enzymes superoxide dismutase (SOD), glutathione (GSH), malondialdehyde (MDA), and inflammatory cytokines (IL-6, IL-B, TNF) using ELISA assay. Pre-treatment with ellagic acid led to a significant decrease in pro-inflammatory cytokines and improved antioxidant enzyme levels compared to the 5-FU group. Histopathological analysis demonstrated the mucoprotective effect of ellagic acid against 5-FU-induced intestinal changes, including villi atrophy, damage to stem cells, infiltration of inflammatory cells in the mucosal layer, edema, damage to muscular mucosa, and decreased oxidative stress production, such as MDA. These results suggest that ellagic acid may be a potential candidate for treating IM induced by antineoplastic drugs.
肠黏膜炎(IM)是多种抗癌药物的常见副作用,包括 5-氟尿嘧啶(5-FU),可导致治疗中断和结局受损。IM 具有严重的临床影响,如腹泻、红斑性黏膜损伤和溃疡形成,伴有剧痛。本研究旨在评估鞣花酸对 5-FU 诱导的小鼠 IM 的黏膜保护作用。小鼠连续 6 天腹腔注射生理盐水,然后连续 4 天腹腔注射 5-FU,剂量为 50mg/kg。鞣花酸在第 III 和第 IV 组中以两种剂量(5mg 和 10mg)口服给予小鼠,与 5-FU 相隔 1 小时,共 10 天。实验结束时,收集小肠组织,用 ELISA 法测定抗氧化酶超氧化物歧化酶(SOD)、谷胱甘肽(GSH)、丙二醛(MDA)和炎症细胞因子(IL-6、IL-B、TNF)的水平。与 5-FU 组相比,鞣花酸预处理可显著降低促炎细胞因子,提高抗氧化酶水平。组织病理学分析表明,鞣花酸对 5-FU 诱导的肠道变化具有黏膜保护作用,包括绒毛萎缩、干细胞损伤、黏膜层炎症细胞浸润、水肿、肌黏膜损伤以及 MDA 等氧化应激产物减少。这些结果表明,鞣花酸可能是治疗抗肿瘤药物诱导的 IM 的潜在候选药物。