Source:http://linkedlifedata.com/resource/pubmed/id/15126243
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2004-8-13
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pubmed:abstractText |
Muscle insulin resistance develops when plasma free fatty acids (FFAs) are acutely increased to supraphysiological levels (approximately 1,500-4,000 micromol/l). However, plasma FFA levels >1,000 micromol/l are rarely observed in humans under usual living conditions, and it is unknown whether insulin action may be impaired during a sustained but physiological FFA increase to levels seen in obesity and type 2 diabetes mellitus (T2DM) (approximately 600-800 micromol/l). It is also unclear whether normal glucose-tolerant subjects with a strong family history of T2DM (FH+) would respond to a low-dose lipid infusion as individuals without any family history of T2DM (CON). To examine these questions, we studied 7 FH+ and 10 CON subjects in whom we infused saline (SAL) or low-dose Liposyn (LIP) for 4 days. On day 4, a euglycemic insulin clamp with [3-3H]glucose and indirect calorimetry was performed to assess glucose turnover, combined with vastus lateralis muscle biopsies to examine insulin signaling. LIP increased plasma FFA approximately 1.5-fold, to levels seen in T2DM. Compared with CON, FH+ were markedly insulin resistant and had severely impaired insulin signaling in response to insulin stimulation. LIP in CON reduced insulin-stimulated glucose disposal (Rd) by 25%, insulin-stimulated insulin receptor tyrosine phosphorylation by 17%, phosphatidylinositol 3-kinase activity associated with insulin receptor substrate-1 by 20%, and insulin-stimulated glycogen synthase fractional velocity over baseline (44 vs. 15%; all P < 0.05). In contrast to CON, a physiological elevation in plasma FFA in FH+ led to no further deterioration in Rd or to any additional impairment of insulin signaling. In conclusion, a 4-day physiological increase in plasma FFA to levels seen in obesity and T2DM impairs insulin action/insulin signaling in CON but does not worsen insulin resistance in FH+. Whether this lack of additional deterioration in insulin signaling in FH+ is due to already well-established lipotoxicity, or to other molecular mechanisms related to insulin resistance that are nearly maximally expressed early in life, remains to be determined.
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pubmed:grant | |
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/C-Peptide,
http://linkedlifedata.com/resource/pubmed/chemical/Fatty Acids, Nonesterified,
http://linkedlifedata.com/resource/pubmed/chemical/Hormones,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0193-1849
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pubmed:author |
pubmed-author:BajajMandeepM,
pubmed-author:BarrentineAndreaA,
pubmed-author:BelfortRenataR,
pubmed-author:BerriaRacheleR,
pubmed-author:CusiKennethK,
pubmed-author:DeFronzoRalphR,
pubmed-author:FinlaysonJeanJ,
pubmed-author:KashyapSangeeta RSR,
pubmed-author:MandarinoLawrenceL,
pubmed-author:PratipranawatrThongchaiT,
pubmed-author:SuraamornkulSwangjitS
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pubmed:issnType |
Print
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pubmed:volume |
287
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
E537-46
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:15126243-Adult,
pubmed-meshheading:15126243-Blood Glucose,
pubmed-meshheading:15126243-C-Peptide,
pubmed-meshheading:15126243-Diabetes Mellitus, Type 2,
pubmed-meshheading:15126243-Fasting,
pubmed-meshheading:15126243-Fatty Acids, Nonesterified,
pubmed-meshheading:15126243-Female,
pubmed-meshheading:15126243-Hormones,
pubmed-meshheading:15126243-Humans,
pubmed-meshheading:15126243-Insulin,
pubmed-meshheading:15126243-Male,
pubmed-meshheading:15126243-Middle Aged,
pubmed-meshheading:15126243-Osmolar Concentration,
pubmed-meshheading:15126243-Reference Values,
pubmed-meshheading:15126243-Signal Transduction,
pubmed-meshheading:15126243-Time Factors
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pubmed:year |
2004
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pubmed:articleTitle |
Discordant effects of a chronic physiological increase in plasma FFA on insulin signaling in healthy subjects with or without a family history of type 2 diabetes.
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pubmed:affiliation |
Diabetes Division, Department of Medicine, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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