Source:http://linkedlifedata.com/resource/pubmed/id/21332399
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2011-2-21
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pubmed:abstractText |
This study evaluated the anti-obesity effects of Phellinus baumii extract (PBE) in high-fat diet (HFD)-fed mice. Male 8-week-old C57BL/6 mice were randomly divided into four groups: control, normal chow diet plus vehicle; HFD-control, high-fat plus vehicle; HFD plus orlistat (Xenical(®), Roche, Basel, Switzerland) (50?mg/kg); and HFD plus PBE (500?mg/kg). PBE was administered daily by oral gavage for 12 weeks. Oral administration of PBE (500?mg/kg) significantly reduced body weight gain, hepatic lipid concentrations, and fat accumulation in epididymal adipocytes compared with mice fed HFD alone (P?<?.05). mRNA expression of genes related to triglyceride (TG) synthesis was suppressed in the PBE groups, and fatty acid synthase activity was also significantly inhibited (P?<?.05). Furthermore, we evaluated the effect of PBE on TG absorption and detected marked reduction in TG absorption in Xenical- and PBE-treated mice compared with the control group (P?<?.05). To determine the active compound of PBE, fractionation was conducted, and interfungin A, davallialactone, and hypholomine B were identified as the main compounds. Among the three identified compounds, as a representative compound, davallialactone was also shown to suppress fat accumulation in an in vitro model system. These anti-obesity and hypolipidemic effects appear to be partly mediated by suppressing plasma and hepatic fat accumulation through the inhibition of enzymes associated with hepatic and intestinal lipid absorption and synthesis.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Obesity Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Biological Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Dietary Fats,
http://linkedlifedata.com/resource/pubmed/chemical/Fatty Acid Synthetase Complex,
http://linkedlifedata.com/resource/pubmed/chemical/Lactones,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides,
http://linkedlifedata.com/resource/pubmed/chemical/orlistat
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1557-7600
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
209-18
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:21332399-Adipocytes,
pubmed-meshheading:21332399-Adipose Tissue,
pubmed-meshheading:21332399-Animals,
pubmed-meshheading:21332399-Anti-Obesity Agents,
pubmed-meshheading:21332399-Basidiomycota,
pubmed-meshheading:21332399-Biological Agents,
pubmed-meshheading:21332399-Dietary Fats,
pubmed-meshheading:21332399-Epididymis,
pubmed-meshheading:21332399-Fatty Acid Synthetase Complex,
pubmed-meshheading:21332399-Intestinal Absorption,
pubmed-meshheading:21332399-Lactones,
pubmed-meshheading:21332399-Lipid Metabolism,
pubmed-meshheading:21332399-Liver,
pubmed-meshheading:21332399-Male,
pubmed-meshheading:21332399-Mice,
pubmed-meshheading:21332399-Mice, Inbred C57BL,
pubmed-meshheading:21332399-Obesity,
pubmed-meshheading:21332399-Phytotherapy,
pubmed-meshheading:21332399-RNA, Messenger,
pubmed-meshheading:21332399-Random Allocation,
pubmed-meshheading:21332399-Triglycerides,
pubmed-meshheading:21332399-Weight Gain
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pubmed:year |
2011
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pubmed:articleTitle |
A Phellinus baumii extract reduces obesity in high-fat diet-fed mice and absorption of triglyceride in lipid-loaded mice.
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pubmed:affiliation |
Animal Model Center, Korea Research Institute of Bioscience and Biotechnology, Iksan, Jeonbuk, Republic of Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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