Metabolic adaptation of the hypertrophied heart:: Role of the malate/aspartate and α-glycerophosphate shuttles

被引:29
作者
Rupert, BE [1 ]
Segar, JL [1 ]
Schutte, BC [1 ]
Scholz, TD [1 ]
机构
[1] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
关键词
energy metabolism; hypertrophy; mitochondria; nicotinamide adenine dinucleotide; NADH shuttles; oxoglutarate/malate carrier; aspartate/glutamate carrier;
D O I
10.1006/jmcc.2000.1257
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Activation of the malate/aspartate and alpha -glycerophosphate shuttles (the NADH shuttles) has been identified in glycolytically active newborn myocardium. The goal of this study was to determine if the NADH shuttles and their regulatory genes are activated in hypertrophied myocardium as substrate utilization shifts away from fatty acids and toward glucose and lactate. Capacity of the shuttles was determined in cardiac mitochondria isolated one week, one month, and three months following aortic banding or sham operation. Myocardial steady-state mRNA and protein levels of regulatory enzymes were also measured. Despite a significant increase in left ventricular mass and activation of the atrial natriuretic peptide gene, no change in malate/ aspartate nor alpha -glycerophosphate shuttle capacity was found at any of the three time points studied. Reactivation of the genes encoding the regulatory inner mitochondrial membrane proteins was not found in the hypertrophied myocardium, though these genes were down regulated one week following aortic-banding. These results suggest that sufficient malate/aspartate and alpha -glycerophosphate shuttle capacity exists in cardiac mitochondria to accommodate increased shuttle nux as hypertrophied myocardium becomes more grycolytically active. (C) 2000 Academic Press.
引用
收藏
页码:2287 / 2297
页数:11
相关论文
共 38 条
[1]   CONTRIBUTION OF OXIDATIVE-METABOLISM AND GLYCOLYSIS TO ATP PRODUCTION IN HYPERTROPHIED HEARTS [J].
ALLARD, MF ;
SCHONEKESS, BO ;
HENNING, SL ;
ENGLISH, DR ;
LOPASCHUK, GD .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (02) :H742-H750
[2]   QUANTITATIVE STRUCTURAL-ANALYSIS OF THE MYOCARDIUM DURING PHYSIOLOGICAL GROWTH AND INDUCED CARDIAC-HYPERTROPHY - A REVIEW [J].
ANVERSA, P ;
RICCI, R ;
OLIVETTI, G .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1986, 7 (05) :1140-1149
[3]  
ANVERSA P, 1976, LAB INVEST, V35, P475
[4]   Fatty acid utilization in the hypertrophied and failing heart: Molecular regulatory mechanisms [J].
Barger, PM ;
Kelly, DP .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1999, 318 (01) :36-42
[5]   Upregulated and downregulated transcription of myocardial genes after pulmonary artery banding in pigs [J].
Bauer, EP ;
Kuki, S ;
Zimmermann, R ;
Schaper, W .
ANNALS OF THORACIC SURGERY, 1998, 66 (02) :527-531
[6]   INCREASED GLYCOLYTIC METABOLISM IN CARDIAC HYPERTROPHY AND CONGESTIVE FAILURE [J].
BISHOP, SP ;
ALTSCHULD, RA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1970, 218 (01) :153-+
[7]  
Bonham MJ, 1996, BIOTECHNIQUES, V21, P57
[8]  
BROWN LJ, 1994, J BIOL CHEM, V269, P14363
[9]   REGULATION OF CARDIAC GENE-EXPRESSION DURING MYOCARDIAL GROWTH AND HYPERTROPHY - MOLECULAR STUDIES OF AN ADAPTIVE PHYSIOLOGICAL-RESPONSE [J].
CHIEN, KR ;
KNOWLTON, KU ;
ZHU, H ;
CHIEN, S .
FASEB JOURNAL, 1991, 5 (15) :3037-3046
[10]   ALTERED GLUCOSE AND FATTY-ACID OXIDATION IN HEARTS OF THE SPONTANEOUSLY HYPERTENSIVE RAT [J].
CHRISTE, ME ;
RODGERS, RL .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1994, 26 (10) :1371-1375