Institute for Nutritional Science, University of Potsdam, Center for Cardiovascular Research, Charité, Berlin, Germany.
J Hypertens. 2010 Aug;28(8):1666-75. doi: 10.1097/HJH.0b013e32833b558c.
The nitric oxide-soluble guanylate cyclase (sGC)-cGMP signal transduction pathway is impaired in different cardiovascular diseases, including pulmonary hypertension, heart failure and arterial hypertension. Riociguat is a novel stimulator of soluble guanylate cyclase (sGC). However, little is known about the effects of sGC stimulators in experimental models of hypertension. We thus investigated the cardio-renal protective effects of riociguat in low-renin and high-renin rat models of hypertension.
The vasorelaxant effect of riociguat was tested in vitro on isolated saphenous artery rings of normal and nitrate tolerant rabbits. The cardiovascular in-vivo effects of sGC stimulation were evaluated in hypertensive renin-transgenic rats treated with the nitric oxide-synthase inhibitor N-nitro-L-arginine methyl ester (L-NAME) (high-renin model) and in rats with 5/6 nephrectomy (low-renin model).
In both animal models, riociguat treatment improved survival and normalized blood pressure. Moreover, in the L-NAME study part, riociguat reduced cardiac target organ damage as indicated by lower plasma ANP, lower relative left ventricular weight and lower cardiac interstitial fibrosis, and reduced renal target organ damage as indicated by lower plasma creatinine and urea, less glomerulosclerosis and less renal interstitial fibrosis. In the 5/6 nephrectomy study part, riociguat reduced cardiac target organ damage as indicated by lower plasma ANP, lower relative left ventricular weight, lower myocyte diameter and lower arterial media/lumen ratio, and reduced renal target organ damage as indicated by improved creatinine clearance and less renal interstitial fibrosis.
We demonstrate for the first time that the novel sGC stimulator riociguat shows in two independent models of hypertension a potent protection against cardiac and renal target organ damage.
一氧化氮-可溶性鸟苷酸环化酶(sGC)-环鸟苷酸(cGMP)信号转导通路在多种心血管疾病中受损,包括肺动脉高压、心力衰竭和动脉高血压。利奥西呱是一种新型可溶性鸟苷酸环化酶(sGC)刺激剂。然而,关于 sGC 刺激剂在高血压实验模型中的作用知之甚少。因此,我们研究了利奥西呱在低肾素和高肾素高血压大鼠模型中的心脏肾脏保护作用。
在正常和硝酸酯耐受的兔离体隐静脉环上检测利奥西呱的血管舒张作用。在接受一氧化氮合酶抑制剂 N-硝基-L-精氨酸甲酯(L-NAME)处理的高血压肾素转基因大鼠(高肾素模型)和 5/6 肾切除术大鼠(低肾素模型)中评估 sGC 刺激的心血管体内作用。
在两种动物模型中,利奥西呱治疗均提高了存活率并使血压正常化。此外,在 L-NAME 研究部分,利奥西呱减少了心脏靶器官损伤,表现为血浆 ANP 降低、左心室相对重量降低和心肌间质纤维化减少,以及肾脏靶器官损伤,表现为血浆肌酐和尿素降低、肾小球硬化减少和肾间质纤维化减少。在 5/6 肾切除术研究部分,利奥西呱减少了心脏靶器官损伤,表现为血浆 ANP 降低、左心室相对重量降低、心肌细胞直径降低和动脉中膜/腔比降低,以及肾脏靶器官损伤,表现为肌酐清除率改善和肾间质纤维化减少。
我们首次证明,新型 sGC 刺激剂利奥西呱在两种独立的高血压模型中均表现出对心脏和肾脏靶器官损伤的强大保护作用。