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J Nutr Biochem ; 94: 108751, 2021 08.
Article in English | MEDLINE | ID: mdl-33915261

ABSTRACT

Diets rich in mono or polyunsaturated fats have been associated with a healthy phenotype, but there is controversial evidence about coconut oil (CO), which is rich in saturated medium-chain fatty acids. Therefore, the purpose of the present work was to study whether different types of oils rich in polyunsaturated (soybean oil, SO), monounsaturated (olive oil, OO), or saturated fatty acids (coconut oil, CO) can regulate the gut microbiota, insulin sensitivity, inflammation, mitochondrial function in wild type and PPARα KO mice. The group that received SO showed the highest microbial diversity, increase in Akkermansia muciniphila, high insulin sensitivity and low grade inflammation, The OO group showed similar insulin sensitivity and insulin signaling than SO, increase in Bifidobacterium, increase in fatty acid oxidation and low grade inflammation. The CO consumption led to the lowest bacterial diversity, a 9-fold increase in the LPS concentration leading to metabolic endotoxemia, hepatic steatosis, increased lipogenesis, highest LDL-cholesterol concentration and the lowest respiratory capacity and fatty acid oxidation in the mitochondria. The absence of PPARα decreased alpha diversity and increased LPS concentration particularly in the CO group, and increased insulin sensitivity in the groups fed SO or OO. These results indicate that consuming mono or polyunsaturated fatty acids produced health benefits at the recommended intake but a high concentration of oils (three times the recommended oil intake in rodents) significantly decreased the microbial alpha-diversity independent of the type of oil.


Subject(s)
Coconut Oil/pharmacology , Gastrointestinal Microbiome/drug effects , Non-alcoholic Fatty Liver Disease/prevention & control , Olive Oil/pharmacology , PPAR alpha/metabolism , Soybean Oil/pharmacology , Animals , Bacteria/classification , Bacteria/genetics , Cells, Cultured , Computational Biology , DNA, Bacterial/genetics , Feces/chemistry , Gene Expression Regulation/drug effects , Genotype , Glucose Intolerance , Hepatocytes/drug effects , Insulin Resistance , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , NF-kappa B/genetics , NF-kappa B/metabolism , Oxygen Consumption/drug effects , PPAR alpha/genetics , RNA, Bacterial/genetics , RNA, Ribosomal, 16S , Random Allocation , Toll-Like Receptor 4/genetics , Toll-Like Receptor 4/metabolism
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