Progressive loss of myocardial ATP due to a loss of total purines during the development of heart failure in dogs - A compensatory role for the parallel loss of creatine

被引:139
作者
Shen, WQ
Asai, K
Uechi, M
Mathier, MA
Shannon, RP
Vatner, SF
Ingwall, JS
机构
[1] Brigham & Womens Hosp, Dept Med, Div Cardiovasc, Physiol Chem Lab,NMR, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Allegheny Univ Hlth Sci, Cardiovasc & Pulm Res Inst, Pittsburgh, PA USA
[4] Penn State Univ, Coll Med, Weis Ctr Res, Hershey, PA 17033 USA
关键词
adenosine triphosphate; purine; creatine; oxygen; heart failure;
D O I
10.1161/01.CIR.100.20.2113
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Whether myocardial ATP content falls in heart failure is a long-standing and controversial issue. The mechanism(s) to explain any decrease in ATP content during heart failure have not been identified. Methods and Results-Cardiac dysfunction, heart failure, and a prolonged steady state of heart failure were induced by chronic right ventricular pacing for 1 to 2 weeks, 3 to 4 weeks, and 7 to 9 weeks in dogs. Cardiac function and myocardial O-2 consumption (MVo(2)) were measured with the dogs in the conscious state. ATP, total purine, and creatine were measured in biopsy specimens obtained at each stage. ATP and the total purine pool progressively fell at rates of 0.12 and 0.15 nmol mg protein(-1).d(-1), despite an increase in MVo(2). The rate of loss of creatine was 1.06 nmol mg protein(-1).d(-1), 7 times faster than the depletion of total purine. Conclusions-(1) ATP contents progressively decreased during heart failure as a result of a loss of the total purine pool. The loss of purines may be due to inhibition of de novo purine synthesis, (2) Loss of creatine is an early marker of heart failure and mmay serve as a compensatory mechanism minimizing the reduction of the total purine pool in the failing heart.
引用
收藏
页码:2113 / 2118
页数:6
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