Nonalcoholic fatty liver disease: Roles of the gut and the liver and metabolic modulation by some dietary factors and especially long‐chain n‐3 PUFA

Nonalcoholic fatty liver disease (NAFLD), including nonalcoholic steatohepatitis (NASH), is the leading cause of chronic liver disease in Western countries. NASH increases the risk for fibrosis, cirrhosis, and hepatocellular carcinoma. The mechanisms underlying the steatosis to NASH transition remai...

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Veröffentlicht in:Molecular nutrition & food research 2016-01, Vol.60 (1), p.147-159
Hauptverfasser: Delarue, Jacques, Lallès, Jean‐Paul
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description Nonalcoholic fatty liver disease (NAFLD), including nonalcoholic steatohepatitis (NASH), is the leading cause of chronic liver disease in Western countries. NASH increases the risk for fibrosis, cirrhosis, and hepatocellular carcinoma. The mechanisms underlying the steatosis to NASH transition remain incompletely understood despite recent progress in cellular and molecular aspects. Our primary aim is to analyze recent advances in understanding deviations in hepatic fat metabolism and the implication of gut physiology and microbiota in this transition. Our second aim is to gather experimental and clinical data on the capability of long‐chain n‐3 PUFA (LC n‐3 PUFA), including docosahexaenoic (DHA) and eicosapentaenoic (EPA) acids to prevent or alleviate NAFLD. Our main conclusions are: (i) increasing data support a pivotal role for the gut toward NASH development; (ii) LC n‐3 PUFA have often proven preventive or therapeutic effect toward NASH development in rodent models. In patients with NASH they appear to have no therapeutic effects, but they could have preventive effects, which require to define better the specific roles, modes of action, and doses of DHA and EPA.
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Nutr. Food Res</addtitle><description>Nonalcoholic fatty liver disease (NAFLD), including nonalcoholic steatohepatitis (NASH), is the leading cause of chronic liver disease in Western countries. NASH increases the risk for fibrosis, cirrhosis, and hepatocellular carcinoma. The mechanisms underlying the steatosis to NASH transition remain incompletely understood despite recent progress in cellular and molecular aspects. Our primary aim is to analyze recent advances in understanding deviations in hepatic fat metabolism and the implication of gut physiology and microbiota in this transition. Our second aim is to gather experimental and clinical data on the capability of long‐chain n‐3 PUFA (LC n‐3 PUFA), including docosahexaenoic (DHA) and eicosapentaenoic (EPA) acids to prevent or alleviate NAFLD. 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Lallès, Jean‐Paul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5724-9aaa34503a1a0b9d33bfa7a75835d554e97c65731db5223d5450e716119f33e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>animal models</topic><topic>Animals</topic><topic>diet</topic><topic>Disease Models, Animal</topic><topic>docosahexaenoic acid</topic><topic>eicosapentaenoic acid</topic><topic>Fatty Acids, Omega-3 - pharmacology</topic><topic>fatty liver</topic><topic>fibrosis</topic><topic>Gastrointestinal Microbiome</topic><topic>Gastrointestinal Tract - drug effects</topic><topic>Gastrointestinal Tract - metabolism</topic><topic>Gastrointestinal Tract - microbiology</topic><topic>Gut</topic><topic>hepatoma</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>lipid metabolism</topic><topic>Liver</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Long-chain n-3 PUFA</topic><topic>mechanism of action</topic><topic>Microbiota</topic><topic>microorganisms</topic><topic>Non-alcoholic Fatty Liver Disease - drug therapy</topic><topic>Nonalcoholic fatty liver disease</topic><topic>omega-3 fatty acids</topic><topic>patients</topic><topic>risk</topic><topic>therapeutics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Delarue, Jacques</creatorcontrib><creatorcontrib>Lallès, Jean‐Paul</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Molecular nutrition &amp; 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subjects animal models
Animals
diet
Disease Models, Animal
docosahexaenoic acid
eicosapentaenoic acid
Fatty Acids, Omega-3 - pharmacology
fatty liver
fibrosis
Gastrointestinal Microbiome
Gastrointestinal Tract - drug effects
Gastrointestinal Tract - metabolism
Gastrointestinal Tract - microbiology
Gut
hepatoma
Humans
Life Sciences
lipid metabolism
Liver
Liver - drug effects
Liver - metabolism
Long-chain n-3 PUFA
mechanism of action
Microbiota
microorganisms
Non-alcoholic Fatty Liver Disease - drug therapy
Nonalcoholic fatty liver disease
omega-3 fatty acids
patients
risk
therapeutics
title Nonalcoholic fatty liver disease: Roles of the gut and the liver and metabolic modulation by some dietary factors and especially long‐chain n‐3 PUFA
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