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Evidence Against an Important Role of Plasma Insulin and Glucagon Concentrations in the Increase in EGP Caused by SGLT2 Inhibitors

机译:血浆胰岛素和胰高血糖素浓度在SGLT2抑制剂引起的血浆胰岛素和胰高血糖素浓度增加中的重要作用

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摘要

Sodium–glucose cotransport 2 inhibitors (SGLT2i) lower plasma glucose but stimulate endogenous glucose production (EGP). The current study examined the effect of dapagliflozin on EGP while clamping plasma glucose, insulin, and glucagon concentrations at their fasting level. Thirty-eight patients with type 2 diabetes received an 8-h measurement of EGP ([3-3H]-glucose) on three occasions. After a 3-h tracer equilibration, subjects received 1) dapagliflozin 10 mg (n = 26) or placebo (n = 12); 2) repeat EGP measurement with the plasma glucose concentration clamped at the fasting level; and 3) repeat EGP measurement with inhibition of insulin and glucagon secretion with somatostatin infusion and replacement of basal plasma insulin and glucagon concentrations. In study 1, the change in EGP (baseline to last hour of EGP measurement) in subjects receiving dapagliflozin was 22% greater (+0.66 ± 0.11 mg/kg/min, P < 0.05) than in subjects receiving placebo, and it was associated with a significant increase in plasma glucagon and a decrease in the plasma insulin concentration compared with placebo. Under glucose clamp conditions (study 2), the change in plasma insulin and glucagon concentrations was comparable in subjects receiving dapagliflozin and placebo, yet the difference in EGP between dapagliflozin and placebo persisted (+0.71 ± 0.13 mg/kg/min, P < 0.01). Under pancreatic clamp conditions (study 3), dapagliflozin produced an initial large decrease in EGP (8% below placebo), followed by a progressive increase in EGP that was 10.6% greater than placebo during the last hour. Collectively, these results indicate that 1) the changes in plasma insulin and glucagon concentration after SGLT2i administration are secondary to the decrease in plasma glucose concentration, and 2) the dapagliflozin-induced increase in EGP cannot be explained by the increase in plasma glucagon or decrease in plasma insulin or glucose concentrations.
机译:钠 - 葡萄糖协同转运2抑制剂(SGLT2i)降低血浆葡萄糖但刺激内源性葡萄糖产生(EGP)。目前的研究审查达格列净的效果上EGP,而在他们的空腹水平夹紧血浆葡萄糖,胰岛素,胰高血糖素的浓度。 38例2型糖尿病三次接收EGP([3-3H] - 葡萄糖)的8小时测量。一个3-H示踪平衡后,受试者接受1)达格列10毫克(N = 26)或安慰剂(n = 12); 2)重复测量EGP与在空腹水平夹持的血浆葡萄糖浓度;和3)重复EGP测量与胰岛素和胰高血糖分泌的抑制生长抑素输注和更换基础血浆胰岛素和胰高血糖素浓度的。在研究1中,在接收达格列净受试者EGP(基线至EGP测量的最后一小时)的变化率为22%以上(0.66±0.11毫克/千克/分钟,P <0.05)比在接受安慰剂的受试者,并将其相关联的与血浆胰高血糖素显著增加,与安慰剂相比在血浆胰岛素浓度的降低。下葡萄糖钳夹条件(研究2)中,血浆胰岛素和胰高血糖浓度的变化为在达帕格列净和安慰剂之间接收达格列和安慰剂,然而差异EGP受试者可比持续(0.71±0.13毫克/千克/分钟,P <0.01 )。下胰钳条件(研究3),达格列净产于EGP的初始大降低(低于安慰剂8%),随后在EGP逐渐增加,这是在最后一小时期间比安慰剂10.6%以上。总的来说,这些结果表明,1)的变化的血浆胰岛素和胰高血糖素浓度SGLT2i给药后是继发于血浆葡萄糖浓度的降低,以及2)在EGP的达帕格列净诱导的增加不能由在等离子体胰高血糖素或减少增加来解释血浆胰岛素或葡萄糖浓度。

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