Open Access Green as soon as Postprint is submitted to ZB.
Mitochondrial adaptation in steatotic mice.
Mitochondrion, DOI: 10.1016/j.mito.2017.08.015 (2018)
Western lifestyle-associated malnutrition causes steatosis that may progress to liver inflammation and mitochondrial dysfunction has been suggested as a key factor in promoting this disease. Here we have molecularly, biochemically and biophysically analyzed mitochondria from steatotic wild type and immune-compromised mice fed a Western diet (WD) - enriched in saturated fatty acids (SFAs). WD-mitochondria demonstrated lipidomic changes, a decreased mitochondrial ATP production capacity and a significant sensitivity to calcium. These changes preceded hepatocyte damage and were not associated with enhanced ROS production. Thus, WD-mitochondria do not promote steatohepatitis per se, but demonstrate bioenergetic deficits and increased sensitivity to stress signals.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
Scopus
Cited By
Cited By
Altmetric
3.226
0.977
1
41
Annotations
Special Publikation
Hide on homepage
Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Mitochondria ; Nafld ; Steatosis ; Western Diet
Language
english
Publication Year
2018
Prepublished in Year
2017
HGF-reported in Year
2017
ISSN (print) / ISBN
1567-7249
e-ISSN
1872-8278
Journal
Mitochondrion
Publisher
Elsevier
Reviewing status
Peer reviewed
Institute(s)
Institute of Molecular Toxicology and Pharmacology (TOX)
CF Metabolomics & Proteomics (CF-MPC)
Institute of Diabetes and Obesity (IDO)
CF Metabolomics & Proteomics (CF-MPC)
Institute of Diabetes and Obesity (IDO)
POF-Topic(s)
30203 - Molecular Targets and Therapies
30201 - Metabolic Health
90000 - German Center for Diabetes Research
30201 - Metabolic Health
90000 - German Center for Diabetes Research
Research field(s)
Enabling and Novel Technologies
Helmholtz Diabetes Center
Helmholtz Diabetes Center
PSP Element(s)
G-505200-003
G-505700-001
G-502200-001
G-501900-221
G-505700-001
G-502200-001
G-501900-221
Scopus ID
85030089564
PubMed ID
28935446
Erfassungsdatum
2017-09-28