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Diurnal variation in skeletal muscle and liver glycogen in humans with normal health and Type 2 diabetes

机译:健康状况正常且患有2型糖尿病的人的骨骼肌和肝糖原的昼夜变化

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In health, food carbohydrate is stored as glycogen in muscle and liver, preventing a deleterious rise in osmotically active plasma glucose after eating. Glycogen concentrations increase sequentially after each meal to peak in the evening, and fall to fasting levels thereafter. Skeletal muscle accounts for the larger part of this diurnal buffering capacity with liver also contributing. The effectiveness of this diurnal mechanism has not been previously studied in Type 2 diabetes. We have quantified the changes in muscle and liver glycogen concentration with C-13 magnetic resonance spectroscopy at 3.0 T before and after three meals consumed at 4 h intervals. We studied 40 (25 males; 15 females) well-controlled Type 2 diabetes subjects on metformin only (HbA1c (glycated haemoglobin) 6.4 +/- 0.07% or 47 +/- 0.8 mmol/mol) and 14 (8 males; 6 females) glucose-tolerant controls matched for age, weight and body mass index (BMI). Muscle glycogen concentration increased by 17% after day-long eating in the control group (68.1 +/- 4.8 to 79.7 +/- 4.2 mmol/l; P=0.006), and this change inversely correlated with homoeostatic model assessment of insulin resistance [HOMA-IR] (r=-0.56; P=0.02). There was no change in muscle glycogen in the Type 2 diabetes group after day-long eating (68.3 +/- 2.6 to 67.1 +/- 2.0 mmol/mol; P=0.62). Liver glycogen rose similarly in normal control (325.9 +/- 25.0 to 388.1 +/- 30.3 mmol/l; P=0.005) and Type 2 diabetes groups (296.1 +/- 16.0 to 350.5 +/- 6.7 mmol/l; P<0.0001). In early Type 2 diabetes, the major physiological mechanism for skeletal muscle postprandial glycogen storage is completely inactive. This is directly related to insulin resistance, although liver glycogen storage is normal.
机译:在健康方面,食物中的碳水化合物以糖原的形式储存在肌肉和肝脏中,防止进食后渗透活性血浆葡萄糖的有害增加。每次用餐后糖原浓度依次增加,到晚上达到峰值,此后降至空腹水平。骨骼肌在昼夜缓冲能力中占很大比例,肝脏也起着重要作用。以前尚未在2型糖尿病中研究这种昼夜机理的有效性。我们用C-13磁共振波谱在3.0 T下以4小时间隔食用三餐前后量化了肌肉和肝糖原浓度的变化。我们仅对二甲双胍(糖化血红蛋白(HbA1c(糖化血红蛋白)6.4 +/- 0.07%或47 +/- 0.8 mmol / mol))研究了40名(25名男性; 15名女性)控制良好的2型糖尿病受试者,以及14名(8名男性; 6名女性) )的葡萄糖耐量对照品符合年龄,体重和体重指数(BMI)。对照组的全天进食后,肌肉糖原浓度增加了17%(68.1 +/- 4.8至79.7 +/- 4.2 mmol / l; P = 0.006),并且该变化与胰岛素抵抗的同质模型评估呈负相关[ HOMA-1R](r = -0.56; P = 0.02)。在一天的进食后,2型糖尿病组的肌肉糖原没有变化(68.3 +/- 2.6至67.1 +/- 2.0 mmol / mol; P = 0.62)。正常对照组(325.9 +/- 25.0至388.1 +/- 30.3 mmol / l; P = 0.005)和2型糖尿病组(296.1 +/- 16.0至350.5 +/- 6.7 mmol / l)中肝糖原的升高相似0.0001)。在早期的2型糖尿病中,骨骼肌餐后糖原存储的主要生理机制是完全无效的。尽管肝糖原存储正常,但这与胰岛素抵抗直接相关。

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