Medicine and Medicine Sub-Specialties Department, Cardio Renal Program, UOC Nephrology, Dialysis and Adult Renal Transplant Program, IRCCS Ca' Granda Foundation, Ospedale Maggiore Policlinico, 20122 Milano, Italy.
U.O. Rehabilitative Cardiology Sacra Famiglia Hospital Fatebenefratelli, 22036 Erba, Italy.
Int J Mol Sci. 2022 Oct 9;23(19):11987. doi: 10.3390/ijms231911987.
In the essential homeostatic role of kidney, two intrarenal mechanisms are prominent: the glomerulotubular balance driving the process of Na and water reabsorption in the proximal tubule, and the tubuloglomerular feedback which senses the Na concentration in the filtrate by the juxtaglomerular apparatus to provide negative feedback on the glomerular filtration rate. In essence, the two mechanisms regulate renal oxygen consumption. The renal hyperfiltration driven by increased glomerular filtration pressure and by glucose diuresis can affect renal O consumption that unleashes detrimental sympathetic activation. The sodium-glucose co-transporters inhibitors (SGLTi) can rebalance the reabsorption of Na coupled with glucose and can restore renal O demand, diminishing neuroendocrine activation. Large randomized controlled studies performed in diabetic subjects, in heart failure, and in populations with chronic kidney disease with and without diabetes, concordantly address effective action on heart failure exacerbations and renal adverse outcomes.
在肾脏的基本稳态作用中,两个肾内机制较为突出:肾小球-小管平衡促使近端小管中钠和水的重吸收过程,以及管球反馈通过肾小球旁器感知滤液中的钠浓度,对肾小球滤过率提供负反馈。从本质上讲,这两个机制调节肾脏的耗氧量。由肾小球滤过压升高和葡萄糖利尿驱动的肾高滤过会影响肾脏的耗氧量,从而引发有害的交感神经激活。钠-葡萄糖协同转运蛋白抑制剂(SGLTi)可以重新平衡与葡萄糖耦联的钠重吸收,并恢复肾脏的耗氧量需求,减少神经内分泌激活。在糖尿病患者、心力衰竭患者以及伴有或不伴有糖尿病的慢性肾脏病患者中进行的大型随机对照研究一致表明,它们对心力衰竭恶化和肾脏不良结局具有有效作用。