Freshly isolated mitochondria from failing human hearts exhibit preserved respiratory function

被引:38
作者
Cordero-Reyes, Andrea M. [1 ]
Gupte, Anisha A. [2 ]
Youker, Keith A. [1 ]
Loebe, Matthias [1 ]
Hsueh, Willa A. [3 ,4 ]
Torre-Amione, Guillermo [1 ,5 ]
Taegtmeyer, Heinrich [6 ]
Hamilton, Dale J. [2 ,4 ]
机构
[1] Weill Cornell Med Coll, Methodist DeBakey Heart & Vasc Inst, New York, NY USA
[2] Weill Cornell Med Coll, Bioenerget Program, Houston Methodist Res Inst, New York, NY USA
[3] Weill Cornell Med Coll, Methodist Diabet & Metab Inst, Houston Methodist Res Inst, New York, NY USA
[4] Weill Cornell Med Coll, Houston Methodist Hosp, Dept Med, New York, NY USA
[5] Tecnol Monteney, Catedra Cardiol & Med Vasc, Nuevo Leon, Mexico
[6] Univ Texas Med Sch Houston, Dept Internal Med, Houston, TX USA
关键词
Human heart failure; Mitochondrial function; Oxidative phosphorylation; Electron transport chain; OXIDATIVE-PHOSPHORYLATION; MOUSE MODEL; FAILURE; CAPACITY; CHAIN; HYPERTROPHY; DYSFUNCTION; MYOCARDIUM; ENERGETICS; MUSCLE;
D O I
10.1016/j.yjmcc.2013.12.029
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In heart failure mitochondria] dysfunction is thought to be responsible for energy depletion and contractile dysfunction. The difficulties in procuring fresh left ventricular (LV) myocardium from humans for assessment of mitochondrial function have resulted in the reliance on surrogate markers of mitochondrial function and limited our understanding of cardiac energetics. We isolated mitochondria from fresh LV wall tissue of patients with heart failure and reduced systolic function undergoing heart transplant or left ventricular assist device placement, and compared their function to mitochondria isolated from the non-failing LV (NFLV) wall tissue with normal systolic function from patients with pulmonary hypertension undergoing heart-lung transplant. We performed detailed mitochondrial functional analyses using 4 substrates: glutamate-malate (GM), pyruvate-malate (PM) palmitoyl camitine-malate (PC) and succinate. NFLV mitochondria showed preserved respiratory control ratios and electron chain integrity with only few differences for the 4 substrates. In contrast, HF mitochondria had greater respiration with GM, PM and PC substrates and higher electron chain capacity for PM than for PC. Surprisingly, HF mitochondria had greater respiratory control ratios and lower ADP-independent state 4 rates than NFLV mitochondria for GM, PM and PC substrates demonstrating that HF mitochondria are capable of coupled respiration ex vivo. Gene expression studies revealed decreased expression of key genes in pathways for oxidation of both fatty acids and glucose. Our results suggest that mitochondria from the failing LV myocardium are capable of tightly coupled respiration when isolated and supplied with ample substrates. Thus energy starvation in the failing heart may be the result of dysregulation of metabolic pathways, impaired substrate supply or reduced mitochondrial number but not the result of reduced mitochondrial electron transport capacity. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:98 / 105
页数:8
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