Source:http://linkedlifedata.com/resource/pubmed/id/15736115
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2005-2-28
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pubmed:abstractText |
The metabolic syndrome is characterized by a blunted insulin-mediated glucose uptake in various cell types. We compared the glucose uptake characteristics of Epstein-Barr virus (EBV)-transformed lymphoblasts obtained from young men with vs without metabolic and cardiovascular evidence of metabolic syndrome. From a population of 218 men, 20- to 25-year-old, 10 men with a systolic blood pressure (BP) > or =130 mm Hg and family history of hypertension were assigned to a high BP (HBP) group, and 10 with a BP < or =110 mm Hg, and no family history of hypertension was assigned to a low BP (LBP) group. Multiple clinical and metabolic characteristics were examined in both groups and compared. Peripheral lymphocytes from HBP and LBP subjects were EBV-transformed, and the glucose transporter (Glut)-mediated glucose uptake from each group was compared in lymphoblasts. Body mass index, fasting glucose, immunoreactive insulin, insulin resistance index based on a homeostasis model assessment (HOMA-R), and total and low-density lipoprotein cholesterol were significantly higher in the HBP than the LBP subgroup (whole-body insulin resistance). Baseline Glut-mediated and Glut-mediated insulin-stimulated glucose uptake by lymphoblasts from the HBP group were significantly lower than by lymphoblasts from the LBP group (cellular insulin resistance). The net increment in Glut-mediated glucose uptake by insulin was inversely correlated with HOMA-R. In conclusion, cellular insulin resistance in EBV-transformed lymphoblasts is associated with young Japanese subjects with HBP. The net increment in Glut-mediated glucose uptake by insulin in lymphoblasts may be a useful intermediate phenotype to study genetic aspects of the metabolic syndrome.
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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/Blood Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol,
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol, LDL,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxyglucose,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin,
http://linkedlifedata.com/resource/pubmed/chemical/Monosaccharide Transport Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0026-0495
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pubmed:author |
pubmed-author:EguchiTakashiT,
pubmed-author:HayashiMatsuhikoM,
pubmed-author:HiraoKeiichiK,
pubmed-author:HiroseHiroshiH,
pubmed-author:KannoYoshihikoY,
pubmed-author:KawabeHiroshiH,
pubmed-author:MaruyamaTatsuyaT,
pubmed-author:MoriiToshiyukiT,
pubmed-author:OgataTsutomuT,
pubmed-author:OhnoYoichiY,
pubmed-author:SaitoIkuoI,
pubmed-author:SarutaTakaoT
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pubmed:issnType |
Print
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pubmed:volume |
54
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
370-5
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:15736115-Adult,
pubmed-meshheading:15736115-Blood Glucose,
pubmed-meshheading:15736115-Body Mass Index,
pubmed-meshheading:15736115-Cell Division,
pubmed-meshheading:15736115-Cell Line, Transformed,
pubmed-meshheading:15736115-Cholesterol,
pubmed-meshheading:15736115-Cholesterol, LDL,
pubmed-meshheading:15736115-Deoxyglucose,
pubmed-meshheading:15736115-Herpesvirus 4, Human,
pubmed-meshheading:15736115-Homeostasis,
pubmed-meshheading:15736115-Humans,
pubmed-meshheading:15736115-Hypertension,
pubmed-meshheading:15736115-Insulin,
pubmed-meshheading:15736115-Insulin Resistance,
pubmed-meshheading:15736115-Lymphocytes,
pubmed-meshheading:15736115-Male,
pubmed-meshheading:15736115-Monosaccharide Transport Proteins
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pubmed:year |
2005
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pubmed:articleTitle |
Cellular insulin resistance in Epstein-Barr virus-transformed lymphoblasts from young insulin-resistant Japanese men.
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pubmed:affiliation |
Department of Internal Medicine, Keio University School of Medicine, Tokyo 160-8582, Japan. tmorii@sc.itc.keio.ac.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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