Suppr超能文献

钠/钙交换体抑制剂 ORM-11035 可改善射血分数保留心力衰竭模型的心脏功能和重构,而不降低血压。

Long-term effects of Na /Ca exchanger inhibition with ORM-11035 improves cardiac function and remodelling without lowering blood pressure in a model of heart failure with preserved ejection fraction.

机构信息

Department of Internal Medicine and Cardiology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Berlin, Germany.

Department of Cardiology, Medical University of Graz, Graz, Austria.

出版信息

Eur J Heart Fail. 2019 Dec;21(12):1543-1552. doi: 10.1002/ejhf.1619. Epub 2019 Nov 24.

Abstract

AIMS

Heart failure with preserved ejection fraction (HFpEF) is increasingly common but there is currently no established pharmacological therapy. We hypothesized that ORM-11035, a novel specific Na /Ca exchanger (NCX) inhibitor, improves cardiac function and remodelling independent of effects on arterial blood pressure in a model of cardiorenal HFpEF.

METHODS AND RESULTS

Rats were subjected to subtotal nephrectomy (NXT) or sham operation. Eight weeks after intervention, treatment for 16 weeks with ORM-11035 (1 mg/kg body weight) or vehicle was initiated. At 24 weeks, blood pressure measurements, echocardiography and pressure-volume loops were performed. Contractile function, Ca transients and NCX-mediated Ca extrusion were measured in isolated ventricular cardiomyocytes. NXT rats (untreated) showed a HFpEF phenotype with left ventricular (LV) hypertrophy, LV end-diastolic pressure (LVEDP) elevation, increased brain natriuretic peptide (BNP) levels, preserved ejection fraction and pulmonary congestion. In cardiomyocytes from untreated NXT rats, early relaxation was prolonged and NCX-mediated Ca extrusion was decreased. Chronic treatment with ORM-11035 significantly reduced LV hypertrophy and cardiac remodelling without lowering systolic blood pressure. LVEDP [14 ± 3 vs. 9 ± 2 mmHg; NXT (n = 12) vs. NXT + ORM (n = 12); P = 0.0002] and BNP levels [71 ± 12 vs. 49 ± 11 pg/mL; NXT (n = 12) vs. NXT + ORM (n = 12); P < 0.0001] were reduced after ORM treatment. LV cardiomyocytes from ORM-treated rats showed improved active relaxation and diastolic cytosolic Ca decay as well as restored NCX-mediated Ca removal, indicating NCX modulation with ORM-11035 as a promising target in the treatment of HFpEF.

CONCLUSION

Chronic inhibition of NCX with ORM-11035 significantly attenuated cardiac remodelling and diastolic dysfunction without lowering systemic blood pressure in this model of HFpEF. Therefore, long-term treatment with selective NCX inhibitors such as ORM-11035 should be evaluated further in the treatment of heart failure.

摘要

目的

射血分数保留型心力衰竭(HFpEF)日益常见,但目前尚无确立的药物治疗方法。我们假设,新型特异的钠/钙交换体(NCX)抑制剂 ORM-11035,可在 HFpEF 的心脏-肾脏模型中独立于对动脉血压的影响,改善心功能和重塑。

方法和结果

大鼠接受部分肾切除术(NXT)或假手术。干预 8 周后,开始用 ORM-11035(1mg/kg 体重)或载体治疗 16 周。在 24 周时,进行血压测量、超声心动图和压力-容积环检查。在分离的心室心肌细胞中测量收缩功能、Ca 瞬变和 NCX 介导的 Ca 外排。未经治疗的 NXT 大鼠表现出 HFpEF 表型,伴有左心室(LV)肥厚、LV 舒张末期压(LVEDP)升高、脑钠肽(BNP)水平升高、射血分数保留和肺充血。未经治疗的 NXT 大鼠的心肌细胞中,早期松弛延长,NCX 介导的 Ca 外排减少。慢性 ORM-11035 治疗显著降低 LV 肥厚和心脏重塑,而不降低收缩压。LVEDP[14±3 对 9±2mmHg;NXT(n=12)对 NXT+ORM(n=12);P=0.0002]和 BNP 水平[71±12 对 49±11pg/mL;NXT(n=12)对 NXT+ORM(n=12);P<0.0001]在 ORM 治疗后降低。来自 ORM 治疗大鼠的 LV 心肌细胞表现出改善的主动松弛和舒张细胞浆 Ca 衰减,以及恢复的 NCX 介导的 Ca 清除,表明 ORM-11035 对 NCX 的调节是 HFpEF 治疗的一个有希望的靶点。

结论

在 HFpEF 的这种模型中,慢性抑制 NCX 用 ORM-11035 可显著减轻心脏重塑和舒张功能障碍,而不降低全身血压。因此,应进一步评估选择性 NCX 抑制剂(如 ORM-11035)的长期治疗,以治疗心力衰竭。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验