SGLT2 inhibition - a novel strategy for diabetes treatment

被引:630
作者
Chao, Edward C. [1 ]
Henry, Robert R.
机构
[1] VA San Diego Healthcare Syst, Sect Endocrinol Metab & Diabet, La Jolla, CA 92161 USA
关键词
GLUCOSE COTRANSPORTER SGLT2; RECESSIVE RENAL GLUCOSURIA; BETA-CELL FAILURE; GLYCEMIC CONTROL; DAPAGLIFLOZIN; MELLITUS; INSULIN; RATS; HYPERGLYCEMIA; TRANSPORTERS;
D O I
10.1038/nrd3180
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Inhibiting sodium-glucose co-transporters (SGLTs), which have a key role in the reabsorption of glucose in the kidney, has been proposed as a novel therapeutic strategy for diabetes. Genetic mutations in the kidney-specific SGLT2 isoform that result in benign renal glycosuria, as well as preclinical and clinical studies with SGLT2 inhibitors in type 2 diabetes, support the potential of this approach. These investigations indicate that elevating renal glucose excretion by suppressing SGLT2 can reduce plasma glucose levels, as well as decrease weight. Although data from ongoing Phase III trials of these agents are needed to more fully assess safety, results suggest that the beneficial effects of SGLT2 inhibition might be achieved without exerting significant side effects-an advantage over many current diabetes medications. This article discusses the role of SGLT2 in glucose homeostasis and the evidence available so far on the therapeutic potential of blocking these transporters in the treatment of diabetes.
引用
收藏
页码:551 / 559
页数:9
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