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Heart Failure With Preserved Ejection Fraction: A Comprehensive Review and Update of Diagnosis, Pathophysiology, Treatment, and Perioperative Implications.射血分数保留的心力衰竭:诊断、病理生理学、治疗和围手术期影响的全面综述和更新。
J Cardiothorac Vasc Anesth. 2021 Jun;35(6):1839-1859. doi: 10.1053/j.jvca.2020.07.016. Epub 2020 Jul 9.
2
Heart failure with preserved ejection fraction diagnosis and treatment: An updated review of the evidence.射血分数保留的心力衰竭的诊断与治疗:证据的最新综述。
Prog Cardiovasc Dis. 2020 Sep-Oct;63(5):570-584. doi: 10.1016/j.pcad.2020.04.011. Epub 2020 May 5.
3
A comparison of the metabolic effects of treadmill and wheel running exercise in mouse model.小鼠模型中跑步机运动和轮转运动的代谢效应比较。
Lab Anim Res. 2020 Feb 7;36:3. doi: 10.1186/s42826-019-0035-8. eCollection 2020.
4
Diagnosis and treatment of heart failure with preserved left ventricular ejection fraction.射血分数保留的心力衰竭的诊断与治疗
World J Cardiol. 2020 Jan 26;12(1):7-25. doi: 10.4330/wjc.v12.i1.7.
5
Heart Rate and Heart Failure With Preserved Ejection Fraction: Time to Slow β-Blocker Use?心率与射血分数保留的心力衰竭:是时候减少β受体阻滞剂的使用了吗?
Circ Heart Fail. 2019 Aug;12(8):e006213. doi: 10.1161/CIRCHEARTFAILURE.119.006213. Epub 2019 Aug 1.
6
Angiotensin-Neprilysin Inhibition in Heart Failure with Preserved Ejection Fraction.血管紧张素-脑啡肽酶抑制剂在射血分数保留的心力衰竭中的应用。
N Engl J Med. 2019 Oct 24;381(17):1609-1620. doi: 10.1056/NEJMoa1908655. Epub 2019 Sep 1.
7
A preclinical model for phenogroup 3 HFpEF.3型射血分数保留的心力衰竭(HFpEF)的临床前模型。
Aging (Albany NY). 2019 Jul 15;11(13):4305-4307. doi: 10.18632/aging.102102.
8
Exercise in Heart Failure-What Is the Optimal Dose to Improve Pathophysiology and Exercise Capacity?心力衰竭中的运动——改善病理生理学和运动能力的最佳剂量是多少?
Curr Heart Fail Rep. 2019 Aug;16(4):98-107. doi: 10.1007/s11897-019-00428-z.
9
Osteopontin Promotes Left Ventricular Diastolic Dysfunction Through a Mitochondrial Pathway.骨桥蛋白通过线粒体途径促进左心室舒张功能障碍。
J Am Coll Cardiol. 2019 Jun 4;73(21):2705-2718. doi: 10.1016/j.jacc.2019.02.074.
10
Carvedilol (CAR) combined with carnosic acid (CAA) attenuates doxorubicin-induced cardiotoxicity by suppressing excessive oxidative stress, inflammation, apoptosis and autophagy.卡维地洛(CAR)与熊果酸(CAA)联合应用可通过抑制过度氧化应激、炎症、细胞凋亡和自噬来减轻阿霉素诱导的心脏毒性。
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卡维地洛与运动联合治疗可改善 Alport 小鼠的收缩功能,但不能改善舒张功能,并降低血浆骨桥蛋白水平。

Carvedilol and exercise combination therapy improves systolic but not diastolic function and reduces plasma osteopontin in Alport mice.

机构信息

Interdisciplinary Stem Cell Institute, University of Miami Leonard M. Miller School of Medicine, Miami, Florida.

Division of Cardiology, Department of Medicine, University of Miami Leonard M. Miller School of Medicine, Miami, Florida.

出版信息

Am J Physiol Heart Circ Physiol. 2021 May 1;320(5):H1862-H1872. doi: 10.1152/ajpheart.00535.2020. Epub 2021 Mar 26.

DOI:10.1152/ajpheart.00535.2020
PMID:33769915
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8163658/
Abstract

There are currently no Food and Drug Administration-approved treatments for heart failure with preserved ejection fraction (HFpEF). Here we compared the effects of exercise with and without α/β-adrenergic blockade with carvedilol in Alport mice, a model of the phenogroup 3 subclass of HFpEF with underlying renal dysfunction. Alport mice were assigned to the following groups: no treatment control ( = 29), carvedilol ( = 11), voluntary exercise ( = 9), and combination carvedilol and exercise ( = 8). Cardiac function was assessed by echocardiography after 4-wk treatments. Running activity of Alport mice was similar to wild types at 1 mo of age but markedly reduced at 2 mo (1.3 ± 0.40 vs. 4.5 ± 1.02 km/day, < 0.05). There was a nonsignificant trend for increased running activity at 2 mo by carvedilol in the combination treatment group. Combination treatments conferred increased body weight of mice (22.0 ± 1.18 vs. 17.8 ± 0.29 g in untreated mice, < 0.01), suggesting improved physiology, and heart rates declined by similar increments in all carvedilol-treatment groups. The combination treatment improved systolic parameters; stroke volume (30.5 ± 1.99 vs. 17.8 ± 0.77 μL, < 0.0001) as well as ejection fraction and global longitudinal strain compared with controls. Myocardial performance index was normalized by all interventions ( < 0.0001). Elevated osteopontin plasma levels in control Alport mice were significantly lowered only by combination treatment, and renal function of the Alport group assessed by urine albumin creatinine ratio was significantly improved by all treatments. The results support synergistic roles for exercise and carvedilol to augment cardiac systolic function of Alport mice with moderately improved renal functions but no change in diastole. In an Alport mouse model of heart failure with preserved ejection fraction (HFpEF), exercise and carvedilol synergistically improved systolic function without affecting diastole. Carvedilol alone or in combination with exercise also improved kidney function. Molecular analyses indicate that the observed improvements in cardiorenal functions were mediated at least in part by effects on serum osteopontin and related inflammatory cytokine cascades. The work presents new potential therapeutic targets and approaches for HFpEF.

摘要

目前,针对射血分数保留的心力衰竭(HFpEF),还没有获得美国食品药品监督管理局(FDA)批准的治疗方法。在这里,我们比较了在 Alport 小鼠中使用和不使用卡维地洛的 α/β-肾上腺素能阻断的运动效果,Alport 小鼠是 HFpEF 表型 3 亚类的模型,其潜在的肾功能障碍。Alport 小鼠被分为以下几组:无治疗对照组( = 29)、卡维地洛组( = 11)、自愿运动组( = 9)和卡维地洛与运动联合组( = 8)。在 4 周的治疗后,通过超声心动图评估心脏功能。1 个月大时,Alport 小鼠的跑步活动与野生型相似,但在 2 个月时明显减少(1.3±0.40 与 4.5±1.02 km/天,<0.05)。在联合治疗组中,卡维地洛有增加跑步活动的趋势,但无统计学意义。联合治疗使小鼠体重增加(22.0±1.18 与未治疗小鼠的 17.8±0.29 相比,<0.01),表明生理状况得到改善,而所有卡维地洛治疗组的心率均有相似程度的下降。联合治疗改善了收缩参数;与对照组相比,心搏量(30.5±1.99 与 17.8±0.77 μL,<0.0001)以及射血分数和整体纵向应变都有所改善。所有干预措施都使心肌做功指数正常化(<0.0001)。仅联合治疗可显著降低对照 Alport 小鼠的骨桥蛋白血浆水平,而所有治疗均可显著改善 Alport 组的尿白蛋白/肌酐比评估的肾功能。结果支持运动和卡维地洛协同作用,增强具有中度改善肾功能的 Alport 小鼠的心脏收缩功能,但不影响舒张功能。在射血分数保留的心力衰竭(HFpEF)的 Alport 小鼠模型中,运动和卡维地洛协同作用改善了收缩功能,而不影响舒张功能。卡维地洛单独或与运动联合使用也改善了肾功能。分子分析表明,心脏和肾脏功能的观察到的改善至少部分是通过对血清骨桥蛋白和相关炎症细胞因子级联的影响介导的。该工作为 HFpEF 提供了新的潜在治疗靶点和方法。