Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan;
TMK Project, Medical Innovation Center, Kyoto University, Kyoto, Japan; and.
Am J Physiol Renal Physiol. 2014 Dec 15;307(12):F1313-22. doi: 10.1152/ajprenal.00521.2014. Epub 2014 Oct 15.
An inhibition in the renin-angiotensin system (RAS) is one of the most widely used therapies to treat chronic kidney disease. However, its effect is occasionally not sufficient and additional treatments may be required. Recently, we reported that nicorandil exhibited renoprotective effects in a mouse model of diabetic nephropathy. Here we examined if nicorandil can provide an additive protection on enalapril in chronic kidney disease. Single treatment with either enalapril or nicorandil significantly ameliorated glomerular and tubulointerstitial injury in the rat remnant kidney while the combination of these two compounds provided additive effects. In addition, an increase in oxidative stress in remnant kidney was also blocked by either enalapril or nicorandil while the combination of the drugs was more potent. A mechanism was likely due for nicorandil to preventing manganase superoxide dismutase (MnSOD) and sirtuin (Sirt)3 from being reduced in injured kidneys. A study with cultured podocytes indicated that the antioxidative effect could be mediated through sulfonylurea receptor (SUR) in the mitochondrial KATP channel since blocking SUR with glibenclamide reduced MnSOD and Sirt3 expression in podocytes. In conclusion, nicorandil may synergize with enalapril to provide superior protection in chronic kidney disease.
肾素-血管紧张素系统(RAS)的抑制是治疗慢性肾脏病最广泛使用的治疗方法之一。然而,其效果偶尔并不充分,可能需要额外的治疗。最近,我们报道了尼可地尔在糖尿病肾病的小鼠模型中具有肾保护作用。在这里,我们研究了尼可地尔是否可以在慢性肾脏病中与依那普利提供额外的保护。依那普利或尼可地尔的单一治疗显著改善了大鼠残肾中的肾小球和肾小管间质损伤,而这两种化合物的联合使用则具有相加作用。此外,残肾中的氧化应激增加也被依那普利或尼可地尔阻断,而药物联合使用的效果更强。一种机制可能是尼可地尔阻止锰超氧化物歧化酶(MnSOD)和沉默调节蛋白(Sirt)3在受损肾脏中被还原。一项对培养的足细胞的研究表明,这种抗氧化作用可能是通过线粒体 KATP 通道中的磺酰脲受体(SUR)介导的,因为用格列本脲阻断 SUR 会降低足细胞中的 MnSOD 和 Sirt3 表达。总之,尼可地尔可能与依那普利协同作用,为慢性肾脏病提供更好的保护。