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协同共生元含有低聚果糖和德氏乳杆菌 CIDCA 133 可缓解小鼠化疗诱导的肠道黏膜炎。

Synergistic synbiotic containing fructooligosaccharides and Lactobacillus delbrueckii CIDCA 133 alleviates chemotherapy-induced intestinal mucositis in mice.

机构信息

Department of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.

Federal Center for Technological Education of Minas Gerais, Department of Biological Sciences, Belo Horizonte, Brazil.

出版信息

World J Microbiol Biotechnol. 2023 Jun 27;39(9):235. doi: 10.1007/s11274-023-03679-0.

Abstract

Intestinal mucositis is a commonly reported side effect in oncology patients undergoing chemotherapy and radiotherapy. Probiotics, prebiotics, and synbiotics have been investigated as alternative therapeutic approaches against intestinal mucositis due to their well-known anti-inflammatory properties and health benefits to the host. Previous studies showed that the potential probiotic Lactobacillus delbrueckii CIDCA 133 and the prebiotic Fructooligosaccharides (FOS) alleviated the 5-Fluorouracil (5-FU) chemotherapy-induced intestinal mucosa damage. Based on these previous beneficial effects, this work evaluated the anti-inflammatory property of the synbiotic formulation containing L. delbrueckii CIDCA 133 and FOS in mice intestinal mucosa inflammation induced by 5-FU. This work showed that the synbiotic formulation was able to modulate inflammatory parameters, including reduction of cellular inflammatory infiltration, gene expression downregulation of Tlr2, Nfkb1, and Tnf, and upregulation of the immunoregulatory Il10 cytokine, thus protecting the intestinal mucosa from epithelial damage caused by the 5-FU. The synbiotic also improved the epithelial barrier function by upregulating mRNA transcript levels of the short chain fatty acid (SCFA)-associated GPR43 receptor and the occludin tight junction protein, with the subsequent reduction of paracellular intestinal permeability. The data obtained showed that this synbiotic formulation could be a promising adjuvant treatment to be explored against inflammatory damage caused by 5-FU chemotherapy.

摘要

肠道黏膜炎是肿瘤患者在接受化疗和放疗时常见的副作用。由于益生菌具有众所周知的抗炎特性和对宿主的健康益处,因此益生菌、益生元和合生菌已被研究作为对抗肠道黏膜炎的替代治疗方法。先前的研究表明,潜在的益生菌德氏乳杆菌 CIDCA 133 和低聚果糖(FOS)减轻了 5-氟尿嘧啶(5-FU)化疗引起的肠道黏膜损伤。基于这些先前的有益效果,本工作评估了含有德氏乳杆菌 CIDCA 133 和 FOS 的合生制剂在 5-FU 诱导的小鼠肠道黏膜炎症中的抗炎特性。本工作表明,合生制剂能够调节炎症参数,包括减少细胞炎症浸润、Tlr2、Nfkb1 和 Tnf 的基因表达下调以及免疫调节 Il10 细胞因子的上调,从而保护肠道黏膜免受 5-FU 引起的上皮损伤。该合生制剂还通过上调与短链脂肪酸(SCFA)相关的 GPR43 受体和紧密连接蛋白 occludin 的 mRNA 转录水平,改善了上皮屏障功能,随后减少了肠道通透性的增加。获得的数据表明,这种合生制剂可能是一种有前途的辅助治疗方法,可用于探索对抗 5-FU 化疗引起的炎症损伤。

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