About: Elevated hepatic DPP4 activity promotes insulin resistance and non-alcoholic fatty liver disease

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Elevated hepatic DPP4 activity promotes insulin resistance and non-alcoholic fatty liver disease Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Elevated hepatic DPP4 activity promotes insulin resistance and non-alcoholic fatty liver disease
Creator	Baumeier, Christian Fritsche, Andreas Fritsche, Louise Häring, Hans-Ulrich Laeger, Thomas Rödiger, Maria Saussenthaler, Sophie Schlüter, Luisa Schürmann, Annette Stefan, Norbert Alaze, Stella Schwenk, Robert
Source	Elsevier; Medline; PMC
abstract	OBJECTIVE: Increased hepatic expression of dipeptidyl peptidase 4 (DPP4) is associated with non-alcoholic fatty liver disease (NAFLD). Whether this is causative for the development of NAFLD is not yet clarified. Here we investigate the effect of hepatic DPP4 overexpression on the development of liver steatosis in a mouse model of diet-induced obesity. METHODS: Plasma DPP4 activity of subjects with or without NAFLD was analyzed. Wild-type (WT) and liver-specific Dpp4 transgenic mice (Dpp4-Liv-Tg) were fed a high-fat diet and characterized for body weight, body composition, hepatic fat content and insulin sensitivity. In vitro experiments on HepG2 cells and primary mouse hepatocytes were conducted to validate cell autonomous effects of DPP4 on lipid storage and insulin sensitivity. RESULTS: Subjects suffering from insulin resistance and NAFLD show an increased plasma DPP4 activity when compared to healthy controls. Analysis of Dpp4-Liv-Tg mice revealed elevated systemic DPP4 activity and diminished active GLP-1 levels. They furthermore show increased body weight, fat mass, adipose tissue inflammation, hepatic steatosis, liver damage and hypercholesterolemia. These effects were accompanied by increased expression of PPARγ and CD36 as well as severe insulin resistance in the liver. In agreement, treatment of HepG2 cells and primary hepatocytes with physiological concentrations of DPP4 resulted in impaired insulin sensitivity independent of lipid content. CONCLUSIONS: Our results give evidence that elevated expression of DPP4 in the liver promotes NAFLD and insulin resistance. This is linked to reduced levels of active GLP-1, but also to auto- and paracrine effects of DPP4 on hepatic insulin signaling.
has issue date	2017-08-04(xsd:dateTime)
bibo:doi	10.1016/j.molmet.2017.07.016
bibo:pmid	29031724
has license	cc-by-nc-nd
sha1sum (hex)	15b009c611ca19c1c8eac1a7f686e03fe2b4e8ee
schema:url	https://doi.org/10.1016/j.molmet.2017.07.016
resource representing a document's title	Elevated hepatic DPP4 activity promotes insulin resistance and non-alcoholic fatty liver disease
has PubMed Central identifier	PMC5641684
has PubMed identifier	29031724
schema:publication	Mol Metab
resource representing a document's body	covid:15b009c611ca19c1c8eac1a7f686e03fe2b4e8ee#body_text
is schema:about of	named entity 'suffering' named entity 'elevated' named entity 'primary' named entity 'insulin' named entity 'activity' named entity 'expression' named entity 'mice' named entity 'liver' named entity 'insulin resistance' named entity 'NAFLD' named entity 'Dpp4' named entity 'effects' covid:arg/15b009c611ca19c1c8eac1a7f686e03fe2b4e8ee named entity 'steatosis' named entity 'DPP4' named entity 'activity' named entity 'PPARg' named entity 'DPP4' named entity 'reduced levels' named entity 'clarified' named entity 'NAFLD' named entity 'elevated' named entity 'experiments' named entity 'non-alcoholic fatty liver disease' named entity 'PPARg' named entity 'liver' named entity 'hepatocytes' named entity 'mice' named entity 'dipeptidyl peptidase 4' named entity 'Plasma' named entity 'Wild-type' named entity 'DPP4' named entity 'NAFLD' named entity 'NAFLD' named entity 'fat' named entity 'liver' named entity 'DPP4' named entity 'body composition' named entity 'hepatic' named entity 'DPP4' named entity 'insulin sensitivity' named entity 'Dpp4' named entity 'NAFLD' named entity 'apical surface' named entity 'steatosis' named entity 'insulin resistance' named entity 'Western diet' named entity 'Hprt' named entity 'hepatic' named entity 'glycine' named entity 'microarray analysis' named entity 'alanine aminotransferase' named entity 'standard curve' named entity 'biomarker' named entity 'mice' named entity 'vena cava' named entity 'penicillin' named entity 'wild-type' named entity 'Plasma' named entity 'liver injury' named entity 'PPARg' named entity 'plasma' named entity 'isoflurane' named entity 'assay' named entity 'Western blotting' named entity 'hepatic' named entity 'Hepatocyte' named entity 'triglyceride' named entity 'triglyceride' named entity 'peroxisome proliferator'

Faceted Search & Find service v1.13.91 as of Mar 24 2020

Alternative Linked Data Documents: Sponger | ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3229 as of Jul 10 2020, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (94 GB total memory)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software