Journal
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
Volume 287, Issue 3, Pages E537-E546Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpendo.00541.2003
Keywords
insulin resistance; free fatty acids; insulin signal transduction
Categories
Funding
- NCRR NIH HHS [M01-RR-01346] Funding Source: Medline
- NIDDK NIH HHS [R01-DK-24092, F32 DK061189] Funding Source: Medline
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Muscle insulin resistance develops when plasma free fatty acids (FFAs) are acutely increased to supraphysiological levels (similar to1,500 - 4,000 mumol/l). However, plasma FFA levels >1,000 mumol/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) (similar to600 - 800 mumol/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-H-3] glucose and indirect calorimetry was performed to assess glucose turnover, combined with vastus lateralis muscle biopsies to examine insulin signaling. LIP increased plasma FFA similar to 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 (R-d) 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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