학술논문

Diet high in linoleic acid dysregulates the intestinal endocannabinoid system and increases susceptibility to colitis in Mice.
Document Type
article
Source
Gut microbes. 15(1)
Subject
Animals
Humans
Mice
Colitis
Inflammatory Bowel Diseases
Soybean Oil
Linoleic Acid
Endocannabinoids
Diet
High-Fat
Gastrointestinal Microbiome
HNF4α
IBD
PUFAs
adherent invasive E.Coli
epithelial barrier function
gut microbiome
metabolomics
olive oil
oxylipins
soybean oil
Complementary and Integrative Health
Crohn's Disease
Inflammatory Bowel Disease
Prevention
Nutrition
Autoimmune Disease
Digestive Diseases
Aetiology
2.1 Biological and endogenous factors
Oral and gastrointestinal
adherent invasive
E .Coli
HNF4 alpha
Microbiology
Language
Abstract
Inflammatory bowel disease (IBD) is a multifactorial disease with increasing incidence in the U.S. suggesting that environmental factors, including diet, are involved. It has been suggested that excessive consumption of linoleic acid (LA, C18:2 omega-6), which must be obtained from the diet, may promote the development of IBD in humans. To demonstrate a causal link between LA and IBD, we show that a high fat diet (HFD) based on soybean oil (SO), which is comprised of ~55% LA, increases susceptibility to colitis in several models, including IBD-susceptible IL10 knockout mice. This effect was not observed with low-LA HFDs derived from genetically modified soybean oil or olive oil. The conventional SO HFD causes classical IBD symptoms including immune dysfunction, increased intestinal epithelial barrier permeability, and disruption of the balance of isoforms from the IBD susceptibility gene Hepatocyte Nuclear Factor 4α (HNF4α). The SO HFD causes gut dysbiosis, including increased abundance of an endogenous adherent invasive Escherichia coli (AIEC), which can use LA as a carbon source. Metabolomic analysis shows that in the mouse gut, even in the absence of bacteria, the presence of soybean oil increases levels of LA, oxylipins and prostaglandins. Many compounds in the endocannabinoid system, which are protective against IBD, are decreased by SO both in vivo and in vitro. These results indicate that a high LA diet increases susceptibility to colitis via microbial and host-initiated pathways involving alterations in the balance of bioactive metabolites of omega-6 and omega-3 polyunsaturated fatty acids, as well as HNF4α isoforms.