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Glycemic Control Determines Hepatic and Peripheral Glucose Effectiveness in Type 2 Diabetic Subjects

机译:血糖控制确定2型糖尿病受试者的肝和外周葡萄糖有效性

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Glucose effectiveness is impaired in type 2 diabetes. We hypothesize that chronic hyperglycemia and hyperlipid-emia contribute importantly to this defect. To test this hypothesis, we compared the effect of acute hyperglycemia on glucose turnover in type 2 diabetic subjects in good control (GC) (n = 14, age 51.7 +- 3.7 years, BMI 28.4 +- 1.0 kg/m~2, HbA_(1c) 5.9 +- 0.2%) and poor control (PC) (n = 10, age 50.0 +- 2.5 years, BMI 27.9 +- 1.5 kg/m~2, HbA_(1c) 9.9 +- 0.6%) with age- and weight-matched nondiabetic subjects (ND) (n = 11, age 47.0 +- 4.4 years, BMI 28.5 +- 1.0 kg/m~2, HbA_(1c) 5.1 +- 0.2%). Fixed hormonal conditions were attained by infusing somatostatin for 6 h with replacement of basal insulin, glucagon, and growth hormone. Glucose fluxes ([3-~3H]glucose) were compared during euglycemic (5 mmol/l, t = 180-240 min) and hyperglycemic (Hy) (10 mmol/1, t = 300-360 min, variable glucose infusion) clamp intervals. Acute hyperglycemia suppressed hepatic glucose production (GP) by 43% and increased peripheral glucose uptake (GU) by 86% in the ND subjects. Conversely, GP failed to suppress ( - 7% ) and GU was suboptimally increased (+34%) in response to Hy in the PC group. However, optimal glycemic control was associated with normal glucose effectiveness in GC subjects (GP -38%, GU +72%; P > 0.05 for GC vs. ND). To determine whether short-term correction of hyperglycemia and/or hyperlip-idemia is sufficient to reverse the impairment in glucose effectiveness, five PC subjects were restudied after 72 h of normoglycemia (~100 mg/dl; variable insulin infusions). These subjects regained normal effectiveness of glucose to suppress GP and stimulate GU and in response to Hy (GP -47%, GU +71%; P > 0.05 vs. baseline studies). Thus, chronic hyperglycemia and/or hyperlip-idemia contribute to impaired effectiveness of glucose in regulating glucose fluxes in type 2 diabetes and hence to worsening of the overall metabolic condition. Short-term normalization of plasma glucose might break the vicious cycle of impaired glucose effectiveness in type 2 diabetes.
机译:在2型糖尿病中,葡萄糖功效受损。我们假设慢性高血糖和高血脂症是造成这一缺陷的重要原因。为了验证这一假设,我们比较了良好控制(GC)中2型糖尿病受试者急性高血糖对血糖转换的影响(n = 14,年龄51.7±3.7岁,BMI 28.4±1.0 kg / m〜2,HbA_ (1c)5.9±-0.2%)和控制不佳(PC)(n = 10,年龄50.0±2.5岁,BMI 27.9±1.5 kg / m〜2,HbA_(1c)9.9±0.6%) -和体重匹配的非糖尿病受试者(ND)(n = 11,年龄47.0 +-4.4岁,BMI 28.5 +-1.0 kg / m〜2,HbA_(1c)5.1 +-0.2%)。通过补充生长激素抑制素6小时并补充基础胰岛素,胰高血糖素和生长激素,可达到固定的荷尔蒙状况。在正常血糖(5 mmol / l,t = 180-240分钟)和高血糖(Hy)(10 mmol / 1,t = 300-360 min,可变葡萄糖输注)期间比较了葡萄糖通量([3-〜3H]葡萄糖)夹紧间隔。急性高血糖症使ND受试者的肝葡萄糖生成(GP)降低了43%,外周葡萄糖摄取(GU)升高了86%。相反,在PC组中,GP不能抑制(-7%),GU对Hy的响应最佳次增高(+ 34%)。但是,最佳的血糖控制与GC受试者的正常血糖有效性相关(GP -38%,GU + 72%; GC vs. ND P> 0.05)。为了确定短期纠正高血糖和/或高脂血症是否足以逆转葡萄糖功效的损害,对正常血糖72小时(约100 mg / dl;可变胰岛素输注)后的5名PC受试者进行了重新研究。这些受试者恢复了葡萄糖抑制GP和刺激GU以及对Hy的反应的正常有效性(GP -47%,GU + 71%; P> 0.05,相对于基线研究)。因此,慢性高血糖症和/或高脂血症导致葡萄糖在调节2型糖尿病中的葡萄糖通量方面的功效受损,并因此导致总体代谢状况的恶化。血浆葡萄糖的短期正常化可能会打破2型糖尿病患者葡萄糖功效受损的恶性循环。

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