粘膜炎
医学
褪黑素
丙二醛
口服
牙周炎
药理学
氧化应激
尼奥体
抗氧化剂
促炎细胞因子
氟辛醇酮
胃肠病学
炎症
内科学
消炎药
脂质过氧化
牙龈炎
口炎
生物利用度
肿瘤坏死因子α
细胞因子
作者
Prangtip Uthaiwat,Jureerut Daduang,Aroonsri Priprem,Chatri Settasatian,Sirinart Chio‐Srichan,Yao-Chang Lee,Pramote Mahakunakorn,Patcharee Boonsiri
标识
DOI:10.2174/1567201817666200525151848
摘要
Background: Oral mucositis, one of the most common complications of 5-Fluorouracil (5-FU) treatment, leads to several problems, including pain, diarrhea and malnutrition, and reduces the quality of life and subsequent treatments. Melatonin, a neurohormone with anti-inflammatory and antioxidant activities, was encapsulated in niosomes and embedded in a mucoadhesive gel formulation as a Melatonin Niosome Gel (MNG) to perform oral mucositis treatment. Objective: This study aimed to investigate the effectiveness of MNG for the treatment of 5-FU-induced oral mucositis in mice. Methods: Oral mucositis was induced in ICR mice by 5-FU and randomly assigned to receive daily applications of the topical oral MNG, a fluocinolone acetonide gel, a blank niosome gel, or no treatment for 5 days in comparison with a normal group. Average body weights, food consumption, and behaviors of the mice as well as microscopic histopathology, Fourier-Transform Infrared Spectroscopy (FTIR) analysis, proinflammatory cytokine levels, and oxidative stress markers of the tongues were monitored and collected after sacrifice. Results: In comparison to the normal group, the average body weights of the 5-FU-MNG mice did not deviate from that of the normal group, nor was there a significant difference in the time to sleep or licking ( p >0.05 for both parameters). In addition, the mice treated with MNG and fluocinolone acetonide did not show significantly different histopathological, FTIR, interleukin-1β or malondialdehyde (MDA) results in the tongues used as the oral tissue samples. Conclusion: Topical MNG potentially inhibits inflammation and lipid oxidative stress in 5-FU-induced oral mucositis.
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