Source:http://linkedlifedata.com/resource/pubmed/id/19250609
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2009-3-2
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pubmed:abstractText |
Peroxisome proliferator-activated receptor alpha and estrogen are believed to be involved in metabolic changes leading to obesity. To test this relationship, we divided female wildtype and PPAR alpha-deficient mice fed on a high fat diet into the following groups: mock-operated, ovariectomized (OVX), and E(2)-treated. The visceral white adipose tissue and plasma cholesterol levels were increased significantly in wild type OVX and decreased in the E(2)-treated group, but interestingly not in PPAR alpha-deficient mice. The mRNA levels of lipoprotein lipase in adipose tissue were also increased in only wild type OVX and decreased significantly in E(2)-treated mice. These novel results suggest the possibility of signaling crosstalk between PPAR alpha and E2, causing obesity in vivo.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1976-6696
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
28
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
91-5
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pubmed:dateRevised |
2009-4-27
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pubmed:meshHeading |
pubmed-meshheading:19250609-Adipose Tissue,
pubmed-meshheading:19250609-Animals,
pubmed-meshheading:19250609-Dietary Fats,
pubmed-meshheading:19250609-Estrogens,
pubmed-meshheading:19250609-Female,
pubmed-meshheading:19250609-Lipoprotein Lipase,
pubmed-meshheading:19250609-Mice,
pubmed-meshheading:19250609-Mice, Inbred C57BL,
pubmed-meshheading:19250609-Mice, Knockout,
pubmed-meshheading:19250609-Obesity,
pubmed-meshheading:19250609-Ovariectomy,
pubmed-meshheading:19250609-PPAR alpha,
pubmed-meshheading:19250609-Signal Transduction
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pubmed:year |
2009
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pubmed:articleTitle |
Signal crosstalk between estrogen and peroxisome proliferator-activated receptor alpha on adiposity.
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pubmed:affiliation |
Department of Toxicology, National Institute of Toxicological Research, Korea Food and Drug Administration, Seoul, Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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