4.7 Article

Blend of organic acids and medium chain fatty acids prevents the inflammatory response and intestinal barrier dysfunction in mice challenged with enterohemorrhagic Escherichia coli O157:H7

期刊

INTERNATIONAL IMMUNOPHARMACOLOGY
卷 58, 期 -, 页码 64-71

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.intimp.2018.03.014

关键词

Tight junction; Medium chain fatty acids; Organic acids; Intestinal permeability

资金

  1. National Natural Science Foundation of China [31472075]
  2. National Key Research and Development project of China [2017YFD0502004]
  3. China Agriculture Research System [CARS36]
  4. Special fund project for Technology Innovation of Hubei Province [2016ABA113]
  5. Hubei Provincial Creative Team Project of Agricultural Science and Technology [2007620]
  6. Fundamental Research Funds for the Central Universities of China [2662017PY017]

向作者/读者索取更多资源

Impaired epithelial barrier function disrupts immune homeostasis and increases inflammation in intestines, leading to many intestinal diseases. The blend of organic acids (OAs) and medium chain fatty acids (MCFAs) has been shown to have synergistic bactericidal effect. In this study, we demonstrated that two blends of OAs and MCFAs (OM1 and OM2) could prevent the inflammatory response and intestinal barrier dysfunction in enterohemorrhagic Escherichia coli (EHEC)-infected mice. Treatments of OM1 and OM2 significantly reduced the body weight loss and production of IL-6 and TNF-alpha induced by EHEC. Mice treated with OM1 and OM2 showed decrease in serum D-lactic concentration, DAO activity and bacterial transfer to liver and spleen. Furthermore, OM1 and OM2 increased the expression of tight junction proteins occludin and ZO-1, mucus protein MUC-2, and host defense peptides mBD1, mBD2 and mBD3. Finally, OM1 and OM2 increased the population of Lactobacillus spp. and Bifidobacterium spp., but decreased that of E. colt in the cecum. These findings indicate that OM1 and OM2 may be used to develop a prophylactic agent for intestinal inflammation and injury in enteric pathogen infection.

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