Source:http://linkedlifedata.com/resource/pubmed/id/20435456
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2011-1-17
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pubmed:abstractText |
Serum adiponectin has been reported to inversely correlate with the degree of adiposity in children. However, the relative contribution of adiponectin-dependent signaling to the development of metabolic syndrome in childhood obesity is unclear. We overfed prepubertal, male Sprague-Dawley rats a high-fat diet via total enteral nutrition. Excessive caloric intake led to obesity, increased body weight and fat mass; dyslipidemia; ectopic fat deposition; and hyperinsulinemia (P<.05). Expression of fatty acid transporter FAT/CD36 was elevated in both liver and skeletal muscle (P<.05). Hepatic Akt phosphorylation was elevated (P<.05) and FoxO1 protein in hepatic nuclear extracts was reduced (P<.05) in the face of hyperinsulinemia, whereas no increase in Akt phosphorylation or decrease in nuclear FoxO1 was observed in skeletal muscle. Overfeeding increased serum adiponectin concentration from 24.6±1.9 ?g/ml to 46.3±5.9 ?g/ml (P<.004), and positively correlated with increased adipose tissue mass. The expression of the inflammatory cytokine tumor necrosis factor ? in the adipose tissue was unchanged. Adiponectin-mediated adenosine monophosphate (AMP) kinase phosphorylation, peroxisome proliferator-activator receptor-? expression and the expression of genes involved in fatty acid oxidation were elevated in both liver and muscle (P<.05). These data (1) demonstrate that excessive intake of a high-fat diet in young rats results in "adiponectin-independent" increases in ectopic fat deposition and hyperinsulinemia, (2) suggest that fatty acid transport is a major mechanism underlying ectopic fat deposition, (3) demonstrate tissue-specific differences in the response of Akt-FoxO signaling to hyperinsulinemia following the development of pediatric obesity and (4) suggest age-related differences in the role of adiponectin in pathological responses associated with obesity.
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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 |
1873-4847
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011 Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
142-52
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pubmed:meshHeading |
pubmed-meshheading:20435456-Adiponectin,
pubmed-meshheading:20435456-Adipose Tissue,
pubmed-meshheading:20435456-Adiposity,
pubmed-meshheading:20435456-Age Factors,
pubmed-meshheading:20435456-Animals,
pubmed-meshheading:20435456-Antigens, CD36,
pubmed-meshheading:20435456-Enteral Nutrition,
pubmed-meshheading:20435456-Fatty Liver,
pubmed-meshheading:20435456-Hyperinsulinism,
pubmed-meshheading:20435456-Lipid Metabolism,
pubmed-meshheading:20435456-Male,
pubmed-meshheading:20435456-Obesity,
pubmed-meshheading:20435456-Overnutrition,
pubmed-meshheading:20435456-Rats,
pubmed-meshheading:20435456-Rats, Sprague-Dawley,
pubmed-meshheading:20435456-Weight Gain
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pubmed:year |
2011
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pubmed:articleTitle |
Hyperinsulinemia and ectopic fat deposition can develop in the face of hyperadiponectinemia in young obese rats.
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pubmed:affiliation |
Arkansas Children's Nutrition Center, Little Rock, AR 72202, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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