Department of Pharmacology, Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, J. Huttlera 4, 31000 Osijek, Croatia.
Department of Pharmacology and Biochemistry, Faculty of Dental Medicine and Health, Josip Juraj Strossmayer University of Osijek, Crkvena 21, 31000 Osijek, Croatia.
Int J Mol Sci. 2019 Nov 20;20(23):5831. doi: 10.3390/ijms20235831.
Diabetic nephropathy (DN) is one of the most perilous side effects of diabetes mellitus type 1 and type 2 (T1DM and T2DM).). It is known that sodium/glucose cotransporter 2 inhibitors (SGLT 2i) and glucagone like peptide-1 receptor agonists (GLP-1 RAs) have renoprotective effects, but the molecular mechanisms are still unknown. In clinical trials GLP-1 analogs exerted important impact on renal composite outcomes, primarily on macroalbuminuria, possibly through suppression of inflammation-related pathways, however enhancement of natriuresis and diuresis is also one of possible mechanisms of nephroprotection. Dapagliflozin, canagliflozin, and empagliflozin are SGLT2i drugs, useful in reducing hyperglycemia and in their potential renoprotective mechanisms, which include blood pressure control, body weight loss, intraglomerular pressure reduction, and a decrease in urinary proximal tubular injury biomarkers. In this review we have discussed the potential synergistic and/or additive effects of GLP 1 RA and SGLT2 inhibitors on the primary onset and progression of kidney disease, and the potential implications on current guidelines of diabetes type 2 management.
糖尿病肾病(DN)是 1 型和 2 型糖尿病(T1DM 和 T2DM)最危险的并发症之一。已知钠/葡萄糖共转运蛋白 2 抑制剂(SGLT2i)和胰高血糖素样肽-1 受体激动剂(GLP-1 RAs)具有肾脏保护作用,但分子机制尚不清楚。在临床试验中,GLP-1 类似物对肾脏复合结局产生了重要影响,主要是对大量白蛋白尿,可能通过抑制炎症相关途径,但增强利钠和利尿也是肾脏保护的可能机制之一。达格列净、卡格列净和恩格列净是 SGLT2i 药物,可有效降低高血糖,其潜在的肾脏保护机制包括控制血压、减轻体重、降低肾小球内压和减少尿近端肾小管损伤生物标志物。在这篇综述中,我们讨论了 GLP-1RA 和 SGLT2i 对肾脏疾病初发和进展的潜在协同和/或相加作用,以及对 2 型糖尿病管理现行指南的潜在影响。