ENERGY RESERVES AND UTILIZATION RATES IN DEVELOPING BRAIN MEASURED INVIVO BY P-31 AND H-1 NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY

被引:24
作者
CORBETT, RJT [1 ]
LAPTOOK, AR [1 ]
GARCIA, D [1 ]
RULEY, JI [1 ]
机构
[1] UNIV TEXAS,SW MED CTR,DEPT PEDIAT,DALLAS,TX 75235
关键词
BRAIN DEVELOPMENT; ENERGY METABOLISM; GLUCOSE; ISCHEMIA; NEONATAL BRAIN PH; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
D O I
10.1038/jcbfm.1993.29
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Age-related changes in cerebral energy utilization were examined in swine, a species whose maximal rate of development is known to occur in the perinatal period. Interleaved in vivo P-31 and H-1 nuclear magnetic resonance spectroscopy was used to measure the rates of change in cerebral concentrations of phosphocreatine (PCr), nucleoside triphosphates, and lactate following complete ischemia, induced via cardiac arrest, in a total of 19 newborn, 10-day-old, and 1-month-old piglets. Preischemic concentrations of these three metabolites plus glucose and glycogen were determined in a separate experiment on 12 piglets whose brains were funnel-frozen in situ. The rate constants for the PCr and ATP decline and lactate increase were determined by nonlinear regression tits to the experimental data, assuming first-order kinetics. The rate constants and preischemic metabolite concentrations were used to calculate the initial flux of high-energy phosphate equivalents (approximately P), which was used as an estimate of cerebral energy utilization at the point when ischemia was initiated. Cerebral energy utilization equaled 6.5 +/- 1.9, 9.5 +/- 3.2, and 15.1 +/- 3.2 mumol approximately P/g/min in newborn, 10-day-old, and 1-month-old piglets, respectively. Within each age group the energy utilization rate was not altered by hyperglycemia-induced increases in cerebral energy reserves, but during hypoglycemia cerebral energy utilization rates decrease. The slope of approximately P versus time decreased with the duration of ischemia, indicating that cerebral energy utilization rates decrease after the first few minutes of ischemia. Newborn piglets had higher cerebral energy utilization rates compared with literature values for newborn rats and mice. This is consistent with the concept that newborns from a species with a perinatal stage of maximal growth and development will have higher cerebral energy demands compared with newborns from a species such as rodents, whose maximal growth occurs postnatally. However, this conclusion remains tentative because literature cerebral utilization rates estimated from the initial slope of approximately P-versus-time plots tend to underestimate the true rate, since the assumption of continued linearity may not be valid for the interval chosen.
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收藏
页码:235 / 246
页数:12
相关论文
共 31 条
[21]   BLOOD-VOLUME IN NEWBORN PIGLETS - EFFECTS OF TIME OF NATURAL CORD RUPTURE, INTRAUTERINE GROWTH-RETARDATION, ASPHYXIA, AND PROSTAGLANDIN-INDUCED PREMATURITY [J].
LINDERKAMP, O ;
BETKE, K ;
GUNTNER, M ;
JAP, GH ;
RIEGEL, KP ;
WALSER, K .
PEDIATRIC RESEARCH, 1981, 15 (01) :53-57
[22]  
Lowry O.H., 1972, FLEXIBLE SYSTEM ENZY
[23]  
LOWRY OH, 1964, J BIOL CHEM, V239, P18
[24]  
PETROFF OAC, 1988, NEUROLOGY, V38, P1569
[25]   OPTIMAL FREEZING CONDITIONS FOR CEREBRAL METABOLITES IN RATS [J].
PONTEN, U ;
RATCHESON, RA ;
SALFORD, LG ;
SIESJO, BK .
JOURNAL OF NEUROCHEMISTRY, 1973, 21 (05) :1127-1138
[26]   EFFECT OF HYPOXIA ON CEREBRAL METABOLITES MEASURED BY PROTON NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY IN RATS [J].
ROSENBERG, GA ;
WHITE, J ;
GASPAROVIC, C ;
CRISOSTOMO, EA ;
GRIFFEY, RH .
STROKE, 1991, 22 (01) :73-79
[27]  
SIMONS GF, 1974, DIFF EQUAT, P35
[28]   SOFTWARE FOR QUANTITATIVE-ANALYSIS BY C-13 FOURIER-TRANSFORM NUCLEAR MAGNETIC-RESONANCE SPECTROMETRY [J].
SOTAK, CH ;
DUMOULIN, CL ;
LEVY, GC .
ANALYTICAL CHEMISTRY, 1983, 55 (04) :782-787
[29]   PRESENCE OF BIOLOGICALLY LABILE COMPOUNDS DURING ISCHEMIA AND THEIR RELATIONSHIP TO EEG IN RAT CEREBRAL-CORTEX AND HYPOTHALAMUS [J].
SWAAB, DF ;
BOER, K .
JOURNAL OF NEUROCHEMISTRY, 1972, 19 (12) :2843-+
[30]   EFFECT OF ISCHEMIA ON METABOLISM OF BRAIN OF NEWBORN MOUSE [J].
THURSTON, JH ;
MCDOUGAL, DB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1969, 216 (02) :348-+