Antunes Maísa Mota, Leocádio Paola Caroline Lacerda, Teixeira Lílian Gonçalves, Leonel Alda Jusceline, Cara Denise Carmona, Menezes Gustavo Batista, Generoso Simone de Vasconcelos, Cardoso Valbert Nascimento, Alvarez-Leite Jacqueline Isaura, Correia Maria Isabel Toulson Davisson
Departamento de Ciência de Alimentos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil
Departamento de Ciência de Alimentos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.
JPEN J Parenter Enteral Nutr. 2016 Feb;40(2):279-86. doi: 10.1177/0148607114567508. Epub 2015 Jan 8.
Mucositis is a common complication in patients undergoing radiotherapy and chemotherapy. It is associated with pain, poor quality of life, and malnutrition, leading to an increased number of hospital admissions and prolonged hospitalization. The use of immunonutrients may be an alternative treatment option, which may help to improve patient outcome.
Here we assessed the impact of L-citrulline (CIT) on a murine model of 5-fluorouracil (5FU)-induced mucositis.
Swiss male mice were randomized into 4 groups: control, CIT, 5FU, and 5FU+CIT. Mice were fed with commercial chow and supplemented with an oral solution of alanine (control and 5FU groups) or CIT (CIT and 5FU+CIT groups). On the seventh day, mice received intraperitoneal phosphate-buffered saline or 5FU (200 mg/kg, single dose) to induce mucositis. On the 10th day, mice were euthanized, and the blood and small intestines were harvested. Body weight, morphology, histopathology score (hematoxylin and eosin) of the small intestine (from 0-12), myeloperoxidase activity, oxidative stress level, and intestinal permeability were assessed.
We observed significant weight loss after the administration of 5FU in both treated and control animals. CIT administration contributed to a partial recovery of the mucosal architecture as well as an intermediate reduction of the histopathologic score, and functional intestinal permeability was partially rescued.
CIT administration attenuated 5FU-mediated damage to the mucosal architecture of the small intestine, decreasing the size of the injured areas and promoting decreased intestinal permeability.
粘膜炎是接受放疗和化疗患者的常见并发症。它与疼痛、生活质量差和营养不良相关,导致住院次数增加和住院时间延长。使用免疫营养物质可能是一种替代治疗选择,有助于改善患者预后。
在此,我们评估了L-瓜氨酸(CIT)对5-氟尿嘧啶(5FU)诱导的小鼠粘膜炎模型的影响。
将瑞士雄性小鼠随机分为4组:对照组、CIT组、5FU组和5FU + CIT组。小鼠喂食商业饲料,并补充丙氨酸口服溶液(对照组和5FU组)或CIT(CIT组和5FU + CIT组)。在第7天,小鼠腹腔注射磷酸盐缓冲盐水或5FU(200 mg/kg,单剂量)以诱导粘膜炎。在第10天,对小鼠实施安乐死,并采集血液和小肠。评估体重、形态、小肠组织病理学评分(苏木精和伊红染色,0 - 12分)、髓过氧化物酶活性、氧化应激水平和肠道通透性。
我们观察到,在接受治疗和未接受治疗的动物中,给予5FU后体重均显著下降。给予CIT有助于粘膜结构部分恢复,组织病理学评分中度降低,并且部分挽救了肠道功能通透性。
给予CIT减轻了5FU介导的小肠粘膜结构损伤,减小了损伤区域的大小,并促进肠道通透性降低。