High-fat/low-carbohydrate diet reduces insulin-stimulated carbohydrate oxidation but stimulates nonoxidative glucose disposal in humans: An important role for skeletal muscle pyruvate dehydrogenase kinase 4

被引:68
作者
Chokkalingam, K.
Jewell, K.
Norton, L.
Littlewood, J.
van Loon, L. J. C.
Mansell, P.
Macdonald, I. A.
Tsintzas, K. [1 ]
机构
[1] Univ Nottingham, Ctr Integrated Syst Biol & Med, Sch Biomed Sci, Inst Clin Res, Nottingham NG7 2UH, England
[2] Queens Med Ctr, Dept Endocrinol & Diabet, Nottingham NG7 2UH, England
[3] Maastricht Univ, Dept Movement Sci Nutr, NL-6200 MD Maastricht, Netherlands
[4] Maastricht Univ, Toxicol Res Inst Maastricht, NL-6200 MD Maastricht, Netherlands
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1210/jc.2006-1592
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Aim: The aim of this report was to study the effect of high-fat (HF)/low-carbohydrate (CHO) diet on regulation of substrate metabolism in humans. Methods: Ten healthy men consumed either a HF (75% energy as fat) or control (35%) diet for 6 d in random order. On d 7, blood glucose disappearance rate (R-d) was determined before and during a hyperinsulinemic euglycemic clamp. Substrate oxidation was determined by indirect calorimetry. Muscle biopsies were obtained prediet, postdiet, and postclamps. Results: Rd was similar under basal conditions but slightly elevated (similar to 10%, P < 0.05) during the last 30 min of the clamp after the HFdiet. HF diet reduced CHO oxidation under basal (by similar to 40%, P < 0.05) and clamp conditions (by similar to 20%, P < 0.05), increased insulin-mediated whole-body nonoxidative glucose disposal (by 30%, P < 0.05) and muscle glycogen storage (by similar to 25%, P < 0.05). Muscle pyruvate dehydrogenase complex activity was blunted under basal and clamp conditions after HF compared with control (P < 0.05) and was accompanied by an approximately 2-fold increase (P < 0.05) in pyruvate dehydrogenase kinase 4 (PDK4) mRNA and protein expression. Conclusion: Short-term HF/low-CHO dietary intake did not induce whole-body insulin resistance, but caused a shift in im glucose metabolism from oxidation to glycogen storage. Insulin-stimulated CHO oxidation and muscle pyruvate dehydrogenase complex activity were blunted after the HF diet. Up-regulation of muscle PDK4 expression was an early molecular adaptation to these changes, and we showed for the first time in healthy humans, unlike insulin-resistant individuals, that insulin can suppress PDK4 but not PDK2 gene expression in skeletal muscle.
引用
收藏
页码:284 / 292
页数:9
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