Department of Medicine, Division of Cardiovascular Medicine, Henry Ford Hospital, Detroit, Michigan.
Department of Medicine, Division of Cardiovascular Medicine, Henry Ford Hospital, Detroit, Michigan.
J Card Fail. 2020 Nov;26(11):987-997. doi: 10.1016/j.cardfail.2020.08.009. Epub 2020 Aug 22.
Sacubitril/valsartan (Sac/Val), a combined angiotensin-II receptor blocker (Val) and neprilysin inhibitor (Sac) in a 1:1 molar ratio, was shown to decrease the risk of cardiovascular death or heart failure (HF) hospitalization in patients with HF and reduced left ventricular (LV) ejection fraction. This study examined the effects of Sac/Val on LV structure, function, and bioenergetics, and on biomarkers of kidney injury and kidney function in dogs with experimental cardiorenal syndrome.
Fourteen dogs with cardiorenal syndrome (coronary microembolization-induced HF and renal dysfunction) were randomized to 3 months Sac/Val therapy (100 mg once daily, n = 7) or no therapy (control, n = 7). LV ejection fraction and troponin-I, as well as biomarkers of kidney injury/function including serum creatinine and urinary kidney injury molecule-1 were measured before and at end of therapy and the change (treatment effect change) calculated. Mitochondrial function measures, including the maximum rate of adenosine triphosphate synthesis, were measured in isolated cardiomyocytes at end of therapy. In Sac/Val dogs, the change in ejection fraction increased compared with controls, 6.9 ± 1.4 vs 0.7 ± 0.6%, P < .002, whereas change in troponin I decreased, -0.16 ± 0.03 vs -0.03 ± 0.02 ng/mL, P < .001. Urinary change in kidney injury molecule 1 decreased in Sac/Val-treated dogs compared with controls, -17.2 ± 7.9 vs 7.7 ± 3.0 mg/mL, P < .007, whereas the change in serum creatinine was not significantly different. Treatment with Sac/Val increased adenosine triphosphate synthesis compared with controls, 3240 ± 121 vs 986 ± 84 RLU/µg protein, P < .05.
In dogs with cardiorenal syndrome, Sac/Val improves LV systolic function, improves mitochondrial function and decreases biomarkers of heart and kidney injury. The results offer mechanistic insights into the benefits of Sac/Val in HF with compromised renal function.
沙库巴曲缬沙坦(Sac/Val),一种血管紧张素受体拮抗剂(缬沙坦,Val)和 Neprilysin 抑制剂(沙库巴曲,Sac)以 1:1 摩尔比结合而成,可降低射血分数降低的心力衰竭(HF)患者的心血管死亡或心力衰竭(HF)住院风险。本研究探讨了沙库巴曲缬沙坦对患有实验性心肾综合征的犬左心室(LV)结构、功能和生物能量以及肾脏损伤和肾功能生物标志物的影响。
14 只患有心肾综合征的犬(冠状动脉微栓塞诱导的 HF 和肾功能障碍)被随机分为 3 个月的沙库巴曲缬沙坦治疗组(每天 100 毫克,n=7)或无治疗组(对照组,n=7)。在治疗前和治疗结束时测量 LV 射血分数和肌钙蛋白 I,以及包括血清肌酐和尿肾损伤分子 1 在内的肾脏损伤/功能生物标志物,并计算变化(治疗效果变化)。在治疗结束时,还测量了分离的心肌细胞中的线粒体功能测量值,包括三磷酸腺苷合成的最大速率。与对照组相比,沙库巴曲缬沙坦组的射血分数变化增加,6.9±1.4%对 0.7±0.6%,P<.002,而肌钙蛋白 I 的变化减少,-0.16±0.03 对-0.03±0.02ng/ml,P<.001。与对照组相比,沙库巴曲缬沙坦治疗组犬的尿肾损伤分子 1 变化减少,-17.2±7.9 对 7.7±3.0mg/ml,P<.007,而血清肌酐的变化无显著差异。与对照组相比,沙库巴曲缬沙坦治疗组的三磷酸腺苷合成增加,3240±121 对 986±84RLU/μg 蛋白,P<.05。
在患有心肾综合征的犬中,沙库巴曲缬沙坦改善 LV 收缩功能,改善线粒体功能,并降低心脏和肾脏损伤的生物标志物。这些结果为沙库巴曲缬沙坦在肾功能受损的心力衰竭中的益处提供了机制见解。