Renal Unit, Department of Health Sciences, "Magna Graecia" University, Catanzaro, Italy.
Department of Health Sciences, "Magna Graecia" University, Catanzaro, Italy.
Pharmacol Res. 2020 Sep;159:105019. doi: 10.1016/j.phrs.2020.105019. Epub 2020 Jun 15.
Diabetes Mellitus (DM) is a chronic and severe metabolic disease, characterized by chronic hyperglycemia due to insulin resistance and/or reduced insulin secretion. Concerning the non-insulin glucose-lowering therapy for diabetes, Dipeptidyl-peptidase-4 (DPP-4) inhibitors, members of the incretin family, represent new agents, capable of a glycemic control improvement with an advantageous safety profile, given the absence of weight gain, the low incidence of hypoglycemia and the good renal tolerance in patients suffering from chronic renal failure. In addition to demonstrating efficacy in glycemic control through inhibition of GLP-1 degradation, DPP-4 inhibitors (DPP-4is) seem to demonstrate pleiotropic effects, which also make them interesting in both diabetic and non-diabetic nephropathies, especially for their capacity of reducing proteinuria. Several studies about diabetic nephropathy on patients' cohorts and murine models have demonstrated a solid direct relationship between DPP-4 activity and urinary albumin excretion (UAE), thus confirming the capacity of DPP-4is to reduce proteinuria; the mechanism responsible for that effect was studied to assess if it was the result of a direct action on renal impairment or a secondary consequence of the better glycemic control related to these agents. As a result of these more in-depth studies, DPP-4is have demonstrated an improvement of renal inflammation markers and consequent proteinuria reduction, regardless of glucose concentrations. Considering the nephroprotective effects of DPP-4is might be glycemic independent, several studies were conducted to prove the validity of the same effects in non-diabetic nephropathies. Among these studies, DPP-4is demonstrated an improvement of various renal inflammatory markers on several models of non-diabetes dependent renal impairment, confirming their capacity to reduce proteinuria, independently from the action on glucose metabolism. The objective of this review is to present and discuss the so far demonstrated antiproteinuric effect of DPP-4is and their effects on diabetic and non-diabetic nephropathies.
糖尿病(DM)是一种慢性且严重的代谢性疾病,其特征为慢性高血糖症,是由于胰岛素抵抗和/或胰岛素分泌减少所致。对于糖尿病的非胰岛素降血糖治疗,二肽基肽酶-4(DPP-4)抑制剂,是肠促胰岛素家族的成员,代表了一类新的药物,它们能够改善血糖控制,同时具有良好的安全性,因为它们不会导致体重增加、低血糖的发生率低,且在患有慢性肾衰竭的患者中具有良好的肾脏耐受性。除了通过抑制 GLP-1 降解来证明在血糖控制方面的疗效外,DPP-4 抑制剂(DPP-4is)似乎还具有多种作用,这也使它们在糖尿病和非糖尿病肾病中都具有吸引力,尤其是因为它们具有降低蛋白尿的能力。关于 DPP-4 抑制剂在糖尿病肾病患者队列和小鼠模型中的多项研究已经证实了 DPP-4 活性与尿白蛋白排泄(UAE)之间存在直接的关系,从而证实了 DPP-4is 降低蛋白尿的能力;为了评估这种作用是否是对肾脏损害的直接作用的结果,还是与这些药物相关的更好血糖控制的次要后果,对其作用机制进行了研究。由于这些更深入的研究,DPP-4is 已被证明可以改善肾脏炎症标志物,从而降低蛋白尿,而与血糖浓度无关。由于 DPP-4is 的肾脏保护作用可能与血糖无关,因此进行了多项研究以证明这些作用在非糖尿病肾病中的有效性。在这些研究中,DPP-4is 在几种非糖尿病依赖的肾功能不全模型中,证明了各种肾脏炎症标志物的改善,证实了它们能够降低蛋白尿,而与葡萄糖代谢的作用无关。本综述的目的是介绍和讨论迄今为止证明的 DPP-4is 的抗蛋白尿作用及其对糖尿病和非糖尿病肾病的作用。