Human brain β-hydroxybutyrate and lactate increase in fasting-induced ketosis

被引:119
作者
Pan, JW
Rothman, DL
Behar, KL
Stein, DT
Hetherington, HP
机构
[1] Brookhaven Natl Lab, Dept Med, Upton, NY 11973 USA
[2] Yale Univ, Dept Radiol, New Haven, CT USA
[3] Yale Univ, Dept Neurol, New Haven, CT USA
[4] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
关键词
ketone body; brain metabolism; lactate; fasting; energetics;
D O I
10.1097/00004647-200010000-00012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ketones are known to constitute an important fraction of fuel for consumption by the brain, with brain ketone content generally thought to be low. However, the recent observation of 1-mmol/L levels of brain beta-hydroxybutyrate (BHB) in children on the ketogenic diet suggests otherwise. The authors report the measurement of brain BHB and lactate in the occipital lobe of healthy adults using high field (4-T) magnetic resonance spectroscopy, measured in the nonfasted state and after 2- and 3-day fasting-induced ketosis. A 9-mL voxel located in the calcarine Fissure was studied, detecting the BHB and lactate upfield resonances using a H-1 homonuclear editing sequence. Plasma BHB levels also were measured. The mean brain BHB concentration increased from a nonfasted level of 0.05 +/- 0.05 to 0.60 +/- 0.26 mmol/L (after second day of fasting), increasing further to 0.98 +/- 0.16 mmol/L (after the third day of fasting). The mean nonfasted brain lactate was 0.69 +/- 0.17 mmol/L, increasing to 1.47 +/- 0.22 mmol./L after the third day. The plasma and brain BHB levels correlated well (r = 0.86) with a brain-plasma slope of 0.26. These data show that brain BHB rises significantly with 2- and 3-day fasting-induced ketosis. The lactate increase likely results from ketones displacing lactate oxidation without altering glucose phosphorylation and glycolysis.
引用
收藏
页码:1502 / 1507
页数:6
相关论文
共 34 条
[1]   Diet-induced ketosis does not cause cerebral acidosis [J].
AlMudallal, AS ;
LaManna, JC ;
Lust, WD ;
Harik, SI .
EPILEPSIA, 1996, 37 (03) :258-261
[2]   KETONE-BODY PRODUCTION AND DISPOSAL - EFFECTS OF FASTING, DIABETES, AND EXERCISE [J].
BALASSE, EO ;
FERY, F .
DIABETES-METABOLISM REVIEWS, 1989, 5 (03) :247-270
[3]   USE OF R-BETA-[1-C-11]HYDROXYBUTYRATE IN PET STUDIES OF REGIONAL CEREBRAL UPTAKE OF KETONE-BODIES IN HUMANS [J].
BLOMQVIST, G ;
THORELL, JO ;
INGVAR, M ;
GRILL, V ;
WIDEN, L ;
STONEELANDER, S .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 269 (05) :E948-E959
[4]   NO EFFECT OF HYPERKETONEMIA ON LOCAL CEREBRAL GLUCOSE-UTILIZATION IN CONSCIOUS RATS [J].
CORDDRY, DH ;
RAPOPORT, SI ;
LONDON, ED .
JOURNAL OF NEUROCHEMISTRY, 1982, 38 (06) :1637-1641
[5]   INHIBITION, BY 2-OXO ACIDS THAT ACCUMULATE IN MAPLE-SYRUP-URINE DISEASE, OF LACTATE, PYRUVATE, AND 3-HYDROXYBUTYRATE TRANSPORT ACROSS THE BLOOD-BRAIN-BARRIER [J].
CREMER, JE ;
TEAL, HM ;
CUNNINGHAM, VJ .
JOURNAL OF NEUROCHEMISTRY, 1982, 39 (03) :674-677
[6]   CHRONIC KETOSIS AND CEREBRAL METABOLISM [J].
DEVIVO, DC ;
LECKIE, MP ;
FERRENDELLI, JS ;
MCDOUGAL, DB .
ANNALS OF NEUROLOGY, 1978, 3 (04) :331-337
[7]   INVIVO DETERMINATION OF CEREBRAL BLOOD-VOLUME WITH RADIOACTIVE OXYGEN-15 IN MONKEY [J].
EICHLING, JO ;
RAICHLE, ME ;
GRUBB, RL ;
LARSON, KB ;
TERPOGOSSIAN, MM .
CIRCULATION RESEARCH, 1975, 37 (06) :707-714
[8]   INDUCTION PROCESSES IN BLOOD-BRAIN TRANSFER OF KETONE-BODIES DURING STARVATION [J].
GJEDDE, A ;
CRONE, C .
AMERICAN JOURNAL OF PHYSIOLOGY, 1975, 229 (05) :1165-1169
[9]   SPATIALLY LOCALIZED H-1-NMR SPECTRA OF METABOLITES IN THE HUMAN-BRAIN [J].
HANSTOCK, CC ;
ROTHMAN, DL ;
PRICHARD, JW ;
JUE, T ;
SHULMAN, RG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (06) :1821-1825
[10]   BRAIN METABOLISM DURING SHORT-TERM STARVATION IN HUMANS [J].
HASSELBALCH, SG ;
KNUDSEN, GM ;
JAKOBSEN, J ;
HAGEMAN, LP ;
HOLM, S ;
PAULSON, OB .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1994, 14 (01) :125-131