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一种新型化疗诱导口腔和肠道黏膜炎的双重小鼠模型的特征描述。

Characterization of a novel dual murine model of chemotherapy-induced oral and intestinal mucositis.

机构信息

Melbourne Dental School, The University of Melbourne, 720 Swanston Street, Carlton, VIC, 3053, Australia.

College of Dentistry, The University of Tikrit, Tikrit, Iraq.

出版信息

Sci Rep. 2023 Jan 25;13(1):1396. doi: 10.1038/s41598-023-28486-3.

Abstract

Oral and intestinal mucositis are debilitating inflammatory diseases observed in cancer patients undergoing chemo-radiotherapy. These are devastating clinical conditions which often lead to treatment disruption affecting underlying malignancy management. Although alimentary tract mucositis involves the entire gastrointestinal tract, oral and intestinal mucositis are often studied independently utilizing distinct organ-specific pre-clinical models. This approach has however hindered the development of potentially effective whole-patient treatment strategies. We now characterize a murine model of alimentary tract mucositis using 5-Fluorouracil (5-FU). Mice were given 5-FU intravenously (50 mg/kg) or saline every 48 h for 2 weeks. Post initial injection, mice were monitored clinically for weight loss and diarrhea. The incidence and extent of oral mucositis was assessed macroscopically. Microscopical and histomorphometric analyses of the tongue and intestinal tissues were conducted at 3 interim time points during the experimental period. Repeated 5-FU treatment caused severe oral and intestinal atrophy, including morphological damage, accompanied by body weight loss and mild to moderate diarrhea in up to 77.8% of mice. Oral mucositis was clinically evident throughout the observation period in 88.98% of mice. Toluidine blue staining of the tongue revealed that the ulcer size peaked at day-14. In summary, we have developed a model reproducing the clinical and histologic features of both oral and intestinal mucositis, which may represent a useful in vivo pre-clinical model for the study of chemotherapy-induced alimentary tract mucositis and the development of preventative therapies.

摘要

口腔和肠道黏膜炎是癌症患者接受放化疗时出现的一种使人虚弱的炎症性疾病。这些都是破坏性的临床病症,常导致治疗中断,影响恶性肿瘤的基础治疗。尽管消化道黏膜炎涉及整个胃肠道,但口腔和肠道黏膜炎通常使用独特的器官特异性临床前模型分别进行研究。这种方法阻碍了潜在有效全患者治疗策略的发展。我们现在使用氟尿嘧啶(5-FU)描述一种消化道黏膜炎的小鼠模型。小鼠每 48 小时静脉内(50mg/kg)或生理盐水(saline)注射一次,共 2 周。初次注射后,监测小鼠的体重减轻和腹泻情况。宏观上评估口腔黏膜炎的发生率和严重程度。在实验期间的 3 个中间时间点,对舌和肠道组织进行显微镜和组织形态计量学分析。重复 5-FU 处理导致严重的口腔和肠道萎缩,包括形态损伤,伴体重减轻和高达 77.8%的小鼠出现轻度至中度腹泻。在 88.98%的小鼠中,口腔黏膜炎在整个观察期间均有临床症状。舌部甲苯胺蓝染色显示溃疡大小在第 14 天达到峰值。总之,我们已经开发出一种可复制口腔和肠道黏膜炎的临床和组织学特征的模型,这可能代表一种用于研究化疗引起的消化道黏膜炎和预防性治疗的有用的体内临床前模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bf4/9876945/7ecf102e047b/41598_2023_28486_Fig1_HTML.jpg

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