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Enhancement of brown fat thermogenesis using chenodeoxycholic acid in mice
JS. Teodoro, P. Zouhar, P. Flachs, K. Bardova, P. Janovska, AP. Gomes, FV. Duarte, AT. Varela, AP. Rolo, CM. Palmeira, J. Kopecký,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 2005 to 5 years ago
ProQuest Central
from 2005-01-01 to 1 year ago
Open Access Digital Library
from 1997-01-01
Medline Complete (EBSCOhost)
from 2005-01-01 to 2015-11-30
Health & Medicine (ProQuest)
from 2005-01-01 to 1 year ago
Psychology Database (ProQuest)
from 2005-01-01 to 1 year ago
Public Health Database (ProQuest)
from 2000-01-01 to 1 year ago
PubMed
24310401
DOI
10.1038/ijo.2013.230
Knihovny.cz E-resources
- MeSH
- Adipose Tissue, White metabolism MeSH
- Diet, High-Fat MeSH
- Energy Metabolism MeSH
- Adipose Tissue, Brown metabolism MeSH
- Ion Channels metabolism MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Chenodeoxycholic Acid metabolism MeSH
- Lipid Metabolism MeSH
- Mitochondrial Proteins metabolism MeSH
- Mice, Inbred C57BL MeSH
- Mice, Obese MeSH
- Mice MeSH
- Obesity metabolism MeSH
- Oxidative Stress MeSH
- Glucose Intolerance metabolism MeSH
- Signal Transduction MeSH
- Thermogenesis * MeSH
- Blotting, Western MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
OBJECTIVE: Besides their role in lipid absorption, bile acids (BAs) can act as signalling molecules. Cholic acid was shown to counteract obesity and associated metabolic disorders in high-fat-diet (cHF)-fed mice while enhancing energy expenditure through induction of mitochondrial uncoupling protein 1 (UCP1) and activation of non-shivering thermogenesis in brown adipose tissue (BAT). In this study, the effects of another natural BA, chenodeoxycholic acid (CDCA), on dietary obesity, UCP1 in both interscapular BAT and in white adipose tissue (brite cells in WAT), were characterized in dietary-obese mice. RESEARCH DESIGN: To induce obesity and associated metabolic disorders, male 2-month-old C57BL/6J mice were fed cHF (35% lipid wt wt(-1), mainly corn oil) for 4 months. Mice were then fed either (i) for 8 weeks with cHF or with cHF with two different doses (0.5%, 1%; wt wt(-1)) of CDCA (8-week reversion); or (ii) for 3 weeks with cHF or with cHF with 1% CDCA, or pair-fed (PF) to match calorie intake of the CDCA mice fed ad libitum; mice on standard chow diet were also used (3-week reversion). RESULTS: In the 8-week reversion, the CDCA intervention resulted in a dose-dependent reduction of obesity, dyslipidaemia and glucose intolerance, which could be largely explained by a transient decrease in food intake. The 3-week reversion revealed mild CDCA-dependent and food intake-independent induction of UCP1-mediated thermogenesis in interscapular BAT, negligible increase of UCP1 in subcutaneous WAT and a shift from carbohydrate to lipid oxidation. CONCLUSIONS: CDCA could reverse obesity in cHF-fed mice, mainly in response to the reduction in food intake, an effect probably occuring but neglected in previous studies using cholic acid. Nevertheless, CDCA-dependent and food intake-independent induction of UCP1 in BAT (but not in WAT) could contribute to the reduction in adiposity and to the stabilization of the lean phenotype.
References provided by Crossref.org
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