Increase in Plasma Endotoxin Concentrations and the Expression of Toll-like Receptors and Suppressor of Cytokine Signaling-3 in Mononuclear Cells After a High-Fat, High-Carbohydrate Meal Implications for insulin resistance

被引:403
作者
Ghanim, Husam [1 ,2 ]
Abuaysheh, Sanaa [1 ,2 ]
Sia, Ching Ling [1 ,2 ]
Korzeniewski, Kelly [1 ,2 ]
Chaudhuri, Ajay [3 ]
Fernandez-Real, Jose Manuel [1 ,2 ]
Dandona, Paresh [1 ,2 ]
机构
[1] SUNY Buffalo, Div Endocrinol Diabet & Metab, Buffalo, NY 14260 USA
[2] Kaleida Hlth, Buffalo, NY USA
[3] Minist Sci, CIBERobn Fisiopatol Obesidad & Nutr, Hosp Girona, Biomed Res Inst Girona, Girona, Spain
关键词
FACTOR-KAPPA-B; PROINFLAMMATORY STATE; METABOLIC SYNDROME; ADIPOSE-TISSUE; OBESE SUBJECTS; INFLAMMATION; ACTIVATION; SENSITIVITY; MONOCYTES; MICE;
D O I
10.2337/dc09-0979
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - To compare the effect of a high-fat, high-carbohydrate meal (HFHC) with that of a high-fiber and fruit meal on the concentrations of endotoxin (lipopolysaccharide vertical bar LPS vertical bar), LPS-binding protein (LBP), the expression of toll-like receptors (TLRs), and the Suppressor of cytokine signaling-3 (SOCS-3) in mononuclear cells. RESEARCH DESIGN AND METHODS - Healthy lean subjects were given 9 10 calories Of either an HFHC meal (n = 10) or an American Heart Association (AHA)-recommended meal rich in fiber and fruit (n = 10) after an overnight fast. Blood was collected before and at 1, 2, and 3 h after the meal. Cellular indexes of oxidative and inflammatory stress; the expression of SOCS-3, TLR2, and TLR4 in mononuclear cells; and plasma concentrations of LPS and LBP were measured. RESULTS - HFHC meal intake induced an increase in plasma LPS concentration and the expression of SOCS-3, TLR2, and TLR4 protein, reactive oxygen species generation, and nuclear factor-kappa B binding activity (P < 0.05 for all). These increases were totally absent after the AHA meal rich in fiber and fruit. CONCLUSIONS - The novel changes described after the HFHC meal elucidate further the mechanisms underlying postprandial inflammation and also provide the first evidence explaining the pathogenesis of insulin and leptin resistance mediated by SOCS-3 after such meals. In contrast, an AHA meal does not induce these effects.
引用
收藏
页码:2281 / 2287
页数:7
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