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Relationships of plasma adiponectin level and adiponectin receptors 1 and 2 gene expression to insulin sensitivity and glucose and fat metabolism in monozygotic and dizygotic twins.

机译:血浆脂联素水平和脂联素受体1和2基因表达与单卵和双卵双胞胎胰岛素敏感性和葡萄糖和脂肪代谢的关系。

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摘要

Context: Adiponectin is a key insulin-sensitizing adipokine acting on muscle metabolism via two specific receptors [adiponectin receptors 1 and 2 (AdipoR1 and AdipoR2, respectively)]. Objectives: The aim of the study was to investigate the genetic and nongenetic control of plasma adiponectin and muscle AdipoR1/R2 gene expression and the impact of these components on in vivo glucose and fat metabolism. Design and Participants: Plasma adiponectin and muscle gene expression of AdipoR1/R2 were measured before and during insulin infusion in 89 young and 69 elderly monozygotic and dizygotic twins. Insulin action, and glucose and fat oxidation rates were determined using hyperinsulinemic euglycemic clamps and indirect calorimetry. Results: We demonstrated a genetic component in the control of plasma adiponectin and AdipoR1/R2 gene expression. Furthermore, levels of adiponectin and AdipoR1/R2 were influenced by age, sex, abdominal obesity, and aerobic capacity. Intrapair correlations in monozygotic twins indicated a nongenetic influence of birth weight on plasma adiponectin and AdipoR2 expression. Nonoxidative glucose metabolism was associated with AdipoR1 and plasma adiponectin, in young and elderly twins, respectively. In addition, plasma adiponectin was related to glucose and fat oxidation in younger subjects. Conclusions: Plasma adiponectin and muscle gene expression of its specific receptors are controlled by genetic and several specific nongenetic factors. The data suggest that the "adiponectin axis" plays a role in in vivo insulin action and nonoxidative glucose metabolism.
机译:背景:脂联素是通过两个特定受体[脂联素受体1和2(分别为AdipoR1和AdipoR2)]作用于肌肉代谢的关键胰岛素敏感性脂肪因子。目的:本研究的目的是研究血浆脂联素和肌肉AdipoR1 / R2基因表达的遗传和非遗传控制,以及这些成分对体内葡萄糖和脂肪代谢的影响。设计和参与者:在89名年轻和69名老年人的单卵双胎和双卵双胎中,在输注胰岛素之前和期间测量了血浆脂联素和AdipoR1 / R2的肌肉基因表达。使用高胰岛素正常血糖钳和间接量热法测定胰岛素作用以及葡萄糖和脂肪的氧化率。结果:我们证明了遗传成分控制血浆脂联素和AdipoR1 / R2基因表达。此外,脂联素和AdipoR1 / R2的水平受年龄,性别,腹部肥胖和有氧运动能力的影响。单卵双胞胎中的配对对相关性表明出生体重对血浆脂联素和AdipoR2表达的非遗传影响。非氧化葡萄糖代谢分别与年轻和老年双胞胎中的AdipoR1和血浆脂联素有关。此外,血浆脂联素与年轻受试者的葡萄糖和脂肪氧化有关。结论:血浆脂联素及其特定受体的肌肉基因表达受遗传和一些特定的非遗传因素控制。数据表明“脂联素轴”在体内胰岛素作用和非氧化性葡萄糖代谢中起作用。

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