Sen Taha, Heerspink Hiddo J L
Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands; The George Institute for Global Health, Sydney, Australia.
Cell Metab. 2021 Apr 6;33(4):732-739. doi: 10.1016/j.cmet.2021.02.016. Epub 2021 Mar 9.
Sodium glucose co-transporter (SGLT) 2 inhibitors reduce the risk of kidney failure in patients with and without type 2 diabetes (T2D). Although the precise underlying mechanisms for these nephroprotective effects are incompletely understood, various hypotheses have been proposed including reductions in intraglomerular pressure through restoration of tubuloglomerular feedback, blood pressure reduction and favorable effects on vascular function, reduction in tubular workload and hypoxia, and metabolic effects resulting in increased autophagy. Here, we review these mechanisms, which may also explain the beneficial effects of SGLT2 inhibitors on kidney function in patients without T2D.
钠-葡萄糖协同转运蛋白(SGLT)2抑制剂可降低2型糖尿病(T2D)患者和非T2D患者肾衰竭的风险。尽管这些肾脏保护作用的确切潜在机制尚未完全明确,但已提出了各种假说,包括通过恢复球管反馈降低肾小球内压力、降低血压以及对血管功能的有利影响、减少肾小管工作负荷和缺氧,以及产生自噬增加的代谢效应。在此,我们综述这些机制,它们或许也能解释SGLT2抑制剂对非T2D患者肾功能的有益作用。