Division of Diabetes, Endocrinology and Metabolism, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Endocrinology. 2020 Aug 1;161(8). doi: 10.1210/endocr/bqaa080.
Selective inhibitors of sodium glucose cotransporter-2 (SGLT2) are widely used for the treatment of type 2 diabetes and act primarily to lower blood glucose by preventing glucose reabsorption in the kidney. However, it is controversial whether these agents also act on the pancreatic islet, specifically the α cell, to increase glucagon secretion. To determine the effects of SGLT2 on human islets, we analyzed SGLT2 expression and hormone secretion by human islets treated with the SGLT2 inhibitor dapagliflozin (DAPA) in vitro and in vivo. Compared to the human kidney, SLC5A2 transcript expression was 1600-fold lower in human islets and SGLT2 protein was not detected. In vitro, DAPA treatment had no effect on glucagon or insulin secretion by human islets at either high or low glucose concentrations. In mice bearing transplanted human islets, 1 and 4 weeks of DAPA treatment did not alter fasting blood glucose, human insulin, and total glucagon levels. Upon glucose stimulation, DAPA treatment led to lower blood glucose levels and proportionally lower human insulin levels, irrespective of treatment duration. In contrast, after glucose stimulation, total glucagon was increased after 1 week of DAPA treatment but normalized after 4 weeks of treatment. Furthermore, the human islet grafts showed no effects of DAPA treatment on hormone content, endocrine cell proliferation or apoptosis, or amyloid deposition. These data indicate that DAPA does not directly affect the human pancreatic islet, but rather suggest an indirect effect where lower blood glucose leads to reduced insulin secretion and a transient increase in glucagon secretion.
钠-葡萄糖协同转运蛋白 2(SGLT2)选择性抑制剂被广泛用于治疗 2 型糖尿病,主要通过阻止肾脏对葡萄糖的重吸收来降低血糖。然而,这些药物是否也作用于胰岛,特别是α细胞,以增加胰高血糖素分泌,这一点存在争议。为了确定 SGLT2 对人胰岛的作用,我们分析了体外和体内用人胰岛 SGLT2 抑制剂达格列净(DAPA)处理后 SGLT2 的表达和激素分泌情况。与人类肾脏相比,人胰岛中 SLC5A2 转录物的表达水平低 1600 倍,且未检测到 SGLT2 蛋白。在体外,DAPA 处理对高、低糖浓度下人胰岛的胰高血糖素或胰岛素分泌均无影响。在移植了人胰岛的小鼠中,1 周和 4 周的 DAPA 处理均未改变空腹血糖、人胰岛素和总胰高血糖素水平。在葡萄糖刺激下,DAPA 处理导致较低的血糖水平和相应较低的人胰岛素水平,无论治疗时间长短。相比之下,在葡萄糖刺激后,DAPA 处理 1 周后总胰高血糖素增加,但 4 周后恢复正常。此外,DAPA 处理对人胰岛移植物的激素含量、内分泌细胞增殖或凋亡或淀粉样蛋白沉积没有影响。这些数据表明,DAPA 不会直接影响人胰岛,而是表明间接作用,即较低的血糖导致胰岛素分泌减少和胰高血糖素分泌短暂增加。