达帕格列嗪
肾葡萄糖重吸收
内分泌学
内科学
医学
2型糖尿病
重吸收
血糖性
糖尿病
排泄
肾
作者
Ralph A. DeFronzo,Marcus Hompesch,Sreeneeranj Kasichayanula,Xiaoni Liu,Ying Hong,Marc Pfister,Linda Morrow,Bruce R. Leslie,David W. Boulton,Agatha Ching,Frank P. LaCreta,Steven C. Griffen
出处
期刊:Diabetes Care
[American Diabetes Association]
日期:2013-06-05
卷期号:36 (10): 3169-3176
被引量:293
摘要
OBJECTIVE: To examine the effect of dapagliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, on the major components of renal glucose reabsorption (decreased maximum renal glucose reabsorptive capacity [TmG], increased splay, and reduced threshold), using the pancreatic/stepped hyperglycemic clamp (SHC) technique. RESEARCH DESIGN AND METHODS: Subjects with type 2 diabetes (n=12) and matched healthy subjects (n=12) underwent pancreatic/SHC (plasma glucose range 5.5-30.5 mmol/L) at baseline and after 7 days of dapagliflozin treatment. A pharmacodynamic model was developed to describe the major components of renal glucose reabsorption for both groups and then used to estimate these parameters from individual glucose titration curves. RESULTS: At baseline, type 2 diabetic subjects had elevated TmG, splay, and threshold compared with controls. Dapagliflozin treatment reduced the TmG and splay in both groups. However, the most significant effect of dapagliflozin was a reduction of the renal threshold for glucose excretion in type 2 diabetic and control subjects. CONCLUSIONS: The SGLT2 inhibitor dapagliflozin improves glycemic control in diabetic patients by reducing the TmG and threshold at which glucose is excreted in the urine.
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