Impact of aging on substrate metabolism by the human heart

被引:142
作者
Kates, AM
Herrero, P
Dence, C
Soto, P
Srinivasan, M
Delano, DG
Ehsani, A
Gropler, RJ
机构
[1] Edward Mallinckrodt Inst Radiol, Cardiovasc Imaging Lab, Div Radiol Sci, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Internal Med, Div Cardiovasc, St Louis, MO 63110 USA
关键词
D O I
10.1016/S0735-1097(02)02714-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Results of studies in experimental animals have shown that, with age, myocardial fatty acid metabolism decreases, and glucose metabolism increases. Whether similar changes occur in humans is unknown. Methods Seventeen healthy younger normal volunteers (six males, 26+/-5 years) and 19 healthy older volunteers (nine males, 67+/-5 years) underwent positron emission tomography (PET) under resting conditions in the fasted state. Myocardial blood flow (MBF), myocardial oxygen consumption (MVO2), myocardial fatty acid utilization (MFAU) and oxidation (MFAO), and myocardial glucose utilization (MGU) were quantified by PET with O-15-water, C-11-acetate, C-11-palmitate, and C-11-glucose, respectively. Results Although MBF was similar between the groups, MVO2 was higher in the older subjects (5.6+/-1.6 mumol/g/min) compared with younger subjects (4.6+/-1.0 mumol/g/min, p<0.04). Rates of MFAU and MFAO (corrected for MVO2) were significantly lower in older subjects than in younger subjects (MFAU/MVO2: 35 +/- 10 vs. 51 +/- 20 nmol free fatty acids (FFA)/nmol O(2)x10(-3), p<0.005, and MFAO/MVO2: 33+/-10 vs. 48+/-18 nmol FFA/nmol O(2)x10(-3), p<0.004). In contrast, the rates of MGU corrected for MVO2 did not differ between the groups. Conclusions With aging, humans exhibit a decline in MFAU and MFAO. Although absolute rates of MGU do not increase, by virtue of the decline in MFAU there is likely an increase in relative contribution of MGU to substrate metabolism. The clinical significance of this metabolic switch awaits further study.
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页码:293 / 299
页数:7
相关论文
共 34 条
[1]   FATTY-ACID OXIDATION BY ISOLATED PERFUSED WORKING HEARTS OF AGED RATS [J].
ABUERREISH, GM ;
NEELY, JR ;
WHITMER, JT ;
WHITMAN, V ;
SANADI, DR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1977, 232 (03) :E258-E262
[2]   NONINVASIVE QUANTITATION OF MYOCARDIAL BLOOD-FLOW IN HUMAN-SUBJECTS WITH OXYGEN-15-LABELED WATER AND POSITRON EMISSION TOMOGRAPHY [J].
BERGMANN, SR ;
HERRERO, P ;
MARKHAM, J ;
WEINHEIMER, CJ ;
WALSH, MN .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1989, 14 (03) :639-652
[3]  
Bergmann SR, 1996, J NUCL MED, V37, P1723
[4]  
BING RJ, 1955, HARVEY LECT, P27
[5]  
BUCK A, 1991, J NUCL MED, V32, P1950
[6]   MYOCARDIAL GLUT-4 GLUCOSE-TRANSPORTER PROTEIN-LEVELS OF RATS DECLINE WITH ADVANCING AGE [J].
CARTEE, GD .
JOURNALS OF GERONTOLOGY, 1993, 48 (04) :B168-B170
[7]   Aging-associated endothelial dysfunction in humans is reversed by L-arginine [J].
Chauhan, A ;
More, RS ;
Mullins, PA ;
Taylor, G ;
Petch, MC ;
Schofield, PM .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1996, 28 (07) :1796-1804
[8]   PREDICTORS OF MORTALITY FROM IDIOPATHIC DILATED CARDIOMYOPATHY IN 356,222 MEN SCREENED FOR THE MULTIPLE RISK FACTOR INTERVENTION TRIAL [J].
COUGHLIN, SS ;
NEATON, JD ;
SENGUPTA, A ;
KULLER, LH .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1994, 139 (02) :166-172
[9]  
CRASS MF, 1969, AM J PHYSIOL, V216, P1569
[10]  
Cupples LA, 1987, SOME RISK FACTORS RE