Effect of xyloglucan associations with gelatin or gelose on Escherichia coli-derived lipopolysaccharide-induced enteritis in rats.

Q2 Pharmacology, Toxicology and Pharmaceutics Drugs in Context Pub Date : 2023-10-26 eCollection Date: 2023-01-01 DOI:10.7573/dic.2023-5-2
Vassilia Theodorou, Catherine Beaufrand, Hélène Eutamene
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Abstract

Background: Escherichia coli is the predominant non-pathogenic facultative microbe of the human intestine, although some strains are diarrhoeagenic in humans. E. coli-derived lipopolysaccharide (LPS) induces diarrhoea, intestinal barrier impairment, bacterial translocation and intestinal inflammation. Associations with the mucoprotectant xyloglucan exhibit antidiarrhoeal effects. This study evaluated and compared the effects of xyloglucan in combination with gelatin or gelose (agar-agar) on jejunal permeability and inflammation using an in vivo rat model of E. coli LPS-induced enteritis.

Methods: Xyloglucan (12.5 mg/kg) plus gelatin (250 mg/kg) or gelose (250 or 500 mg/kg) were administered orally 2 hours before intraperitoneal injection with E. coli LPS. Following euthanasia, jejunal segments were removed for intestinal permeability measurement in Ussing chambers and inflammatory tone evaluation by myeloperoxidase activity assay.

Results: LPS administration increased jejunal permeability and increased mucosal inflammation in male Wistar rats. Xyloglucan plus gelatin 250 mg/kg and xyloglucan plus gelose 500 mg/kg significantly attenuated LPS-induced jejunal hyperpermeability and myeloperoxidase activity.

Conclusion: Xyloglucan, a known mucosal barrier protector, in combination with gelatin or gelose, has beneficial and comparable effects on intestinal permeability and inflammation following E. coli LPS insult in male rats.

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木葡聚糖与明胶或凝胶糖结合对大肠杆菌脂多糖诱导的大鼠肠炎的影响。
背景:大肠杆菌是人类肠道中主要的非致病性兼性微生物,尽管有些菌株在人类中会引起腹泻。大肠杆菌衍生的脂多糖(LPS)可诱导腹泻、肠道屏障损伤、细菌移位和肠道炎症。和粘膜保护剂木葡聚糖的结合物具有抗腹泻作用。本研究使用大肠杆菌LPS诱导肠炎的体内大鼠模型,评估并比较了木葡聚糖与明胶或凝胶(琼脂)联合使用对空肠通透性和炎症的影响。方法:在腹腔注射大肠杆菌LPS前2小时,口服木葡糖(12.5 mg/kg)加明胶(250 mg/kg)或凝胶糖(250或500 mg/kg)。安乐死后,取下空肠段,在Using腔中测量肠道通透性,并通过髓过氧化物酶活性测定评估炎症反应。结果:LPS给药增加了雄性Wistar大鼠的空肠通透性,并增加了粘膜炎症。木葡糖加明胶250mg/kg和木葡聚糖加凝胶糖500mg/kg显著减弱LPS诱导的空肠高渗透性和髓过氧化物酶活性。结论:木葡甘是一种已知的粘膜屏障保护剂,与明胶或凝胶糖联合使用,对雄性大鼠大肠杆菌LPS损伤后的肠道通透性和炎症具有有益和可比的作用。
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来源期刊
Drugs in Context
Drugs in Context Medicine-Medicine (all)
CiteScore
5.90
自引率
0.00%
发文量
63
审稿时长
9 weeks
期刊介绍: Covers all phases of original research: laboratory, animal and human/clinical studies, health economics and outcomes research, and postmarketing studies. Original research that shows positive or negative results are welcomed. Invited review articles may cover single-drug reviews, drug class reviews, latest advances in drug therapy, therapeutic-area reviews, place-in-therapy reviews, new pathways and classes of drugs. In addition, systematic reviews and meta-analyses are welcomed and may be published as original research if performed per accepted guidelines. Editorials of key topics and issues in drugs and therapeutics are welcomed. The Editor-in-Chief will also consider manuscripts of interest in areas such as technologies that support diagnosis, assessment and treatment. EQUATOR Network reporting guidelines should be followed for each article type. GPP3 Guidelines should be followed for any industry-sponsored manuscripts. Other Editorial sections may include Editorial, Case Report, Conference Report, Letter-to-the-Editor, Educational Section.
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