Joshua W-H Chang, Siyi Chen, Charlotte Hamilton, Julia Shanks, Mridula Pachen, Audrys Pauza, Bindu George, Rohit Ramchandra
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The hypertensive HFpEF sheep were characterized by (i) echocardiographic evidence of diastolic dysfunction (lateral e' = 0.11±0.02 vs 0.14±0.04 m/s, <i>P</i> = 0.011; lateral E/e' = 4.25±0.77 vs 3.63±0.54, <i>P</i> = 0.028) and concentric left ventricular hypertrophy without overt systolic impairment, (ii) elevated directly measured left ventricular end-diastolic pressure (13±5 vs 0.5±1 mmHg, <i>P</i> = 2.1x10<sup>-6</sup>), and (iii) normal directly measured cardiac output. Crucially, these hypertensive HFpEF sheep had impaired exercise capacity as demonstrated by their (i) attenuated cardiac output (<i>P</i> = 0.001), (ii) augmented pulmonary capillary wedge pressure (<i>P</i> = 0.026), and (iii) attenuated hindlimb blood flow (<i>P</i> = 3.4x10<sup>-4</sup>) responses, during graded treadmill exercise testing. In addition, exercise renal blood flow responses were also altered. Collectively, our data indicates that this novel ovine model of HFpEF may be a useful translational research tool since it exhibits similar and clinically relevant impairments as that of HFpEF patients.</p>","PeriodicalId":7692,"journal":{"name":"American journal of physiology. 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引用次数: 0
摘要
缺乏能准确代表射血分数保留型心力衰竭(HFpEF)的动物模型,一直是人们从机理上理解这种以多系统损伤为特征的普遍衰弱综合征并开发有效疗法的主要障碍。在本文中,我们描述了一种新型大型高频肾衰竭动物模型的开发和特征描述,该模型以患有慢性双肾一夹高血压的老年雌性绵羊为研究对象。在单侧肾动脉剪切后六周,高血压 HFpEF 羊的平均动脉压高于未剪切单侧肾动脉的同龄母羊(平均动脉压 = 112.7±15.9 vs 76.0±10.1 mmHg,P < 0.0001)。高血压 HFpEF 羊的特点是:(i) 超声心动图显示舒张功能障碍(侧位 e' = 0.11±0.02 vs 0.14±0.04 m/s,P = 0.011;侧位 E/e' = 4.25±0.77 vs 3.63±0.54,P = 0.(ii)直接测量的左心室舒张末压升高(13±5 vs 0.5±1 mmHg,P = 2.1x10-6),(iii)直接测量的心输出量正常。重要的是,这些高血压 HFpEF 羊的运动能力受损,表现在它们在分级跑步机运动测试中:(i) 心输出量降低(P = 0.001);(ii) 肺毛细血管楔压升高(P = 0.026);(iii) 后肢血流量降低(P = 3.4x10-4)。此外,运动肾血流反应也发生了改变。总之,我们的数据表明,这种新型高频肾衰竭绵羊模型可能是一种有用的转化研究工具,因为它表现出与高频肾衰竭患者相似且与临床相关的损伤。
Characterization of a novel ovine model of hypertensive heart failure with preserved ejection fraction.
The lack of animal models which accurately represent heart failure with preserved ejection fraction (HFpEF) has been a major barrier to the mechanistic understanding and development of effective therapies for this prevalent and debilitating syndrome characterized by multisystem impairments. Herein, we describe the development and characterization of a novel large animal model of HFpEF in older, female sheep with chronic 2-kidney, 1-clip hypertension. At six weeks post-unilateral renal artery clipping, hypertensive HFpEF sheep had higher mean arterial pressure compared to similarly aged ewes without unilateral renal artery clipping (mean arterial pressure = 112.7±15.9 vs 76.0±10.1 mmHg, P < 0.0001). The hypertensive HFpEF sheep were characterized by (i) echocardiographic evidence of diastolic dysfunction (lateral e' = 0.11±0.02 vs 0.14±0.04 m/s, P = 0.011; lateral E/e' = 4.25±0.77 vs 3.63±0.54, P = 0.028) and concentric left ventricular hypertrophy without overt systolic impairment, (ii) elevated directly measured left ventricular end-diastolic pressure (13±5 vs 0.5±1 mmHg, P = 2.1x10-6), and (iii) normal directly measured cardiac output. Crucially, these hypertensive HFpEF sheep had impaired exercise capacity as demonstrated by their (i) attenuated cardiac output (P = 0.001), (ii) augmented pulmonary capillary wedge pressure (P = 0.026), and (iii) attenuated hindlimb blood flow (P = 3.4x10-4) responses, during graded treadmill exercise testing. In addition, exercise renal blood flow responses were also altered. Collectively, our data indicates that this novel ovine model of HFpEF may be a useful translational research tool since it exhibits similar and clinically relevant impairments as that of HFpEF patients.
期刊介绍:
The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.