Norepinephrine spillover from human adipose tissue before and after a 72-hour fast

被引:37
作者
Patel, JN
Coppack, SW
Goldstein, DS
Miles, JM
Eisenhofer, G
机构
[1] Natl Inst Neurol Disorders & Stroke, NIH, Clin Neurocardiol Sect, Bethesda, MD 20892 USA
[2] St Bartholomews & Royal London Sch Med, London E1 1BB, England
[3] Mayo Clin, Endocrine Res Unit, Rochester, MN 55905 USA
关键词
D O I
10.1210/jc.87.7.3373
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adipose tissue lipolysis is at least in part stimulated by the sympathetic nervous system (SNS). Although there is a generalized decrease in SNS activity with fasting, the rate of lipolysis during fasting increases. The aim of this study was to determine whether there is an association between activation of sympathetic nerves innervating adipose tissue and the increase in lipolysis seen during fasting in humans. We used the isotope dilution technique to measure regional norepinephrine spillover from abdominal se adipose tissue from seven healthy subjects before and after a 72-h fast. Our results showed a significant increase in adipose tissue spillover of norepinephrine (mean +/- SEM, 0.40 +/- 0.09 vs. 1.08 +/- 0.18 pmol (.)100 g(-1.)min(-1), P < 0.05) and arterial norepinephrine concentrations (0.92 +/- 0.10 vs. 1.23 +/- 0.08 nmol-liter(-1), P < 0.05) after the fast with no significant change in total body norepinephrine spillover, forearm norepinephrine spillover, epinephrine concentrations, or energy expenditure. We show for the first time, in humans, a selective regional increase in adipose tissue norepinephrine spillover in response to a 72-h fast and suggest that the SNS may play a greater role in the regulation of lipid metabolism during fasting than previously thought.
引用
收藏
页码:3373 / 3377
页数:5
相关论文
共 34 条
[1]   IMPEDANCE PLETHYSMOGRAPHY - CAN IT MEASURE CHANGES IN LIMB BLOOD-FLOW [J].
BROWN, BH ;
PRYCE, WIJ ;
BAUMBER, D ;
CLARKE, RG .
MEDICAL & BIOLOGICAL ENGINEERING, 1975, 13 (05) :674-682
[2]  
Bülow J, 2000, METH MOL B, V155, P281
[3]   HORMONE-FUEL INTERRELATIONSHIPS DURING FASTING [J].
CAHILL, GF ;
HERRERA, MG ;
MORGAN, AP ;
SOELDNER, JS ;
STEINKE, J ;
LEVY, PL ;
REICHARD, GA ;
KIPINS, DM .
JOURNAL OF CLINICAL INVESTIGATION, 1966, 45 (11) :1751-+
[4]   Lipolytic effects of β1-, β2-, and β3-adrenergic agonists in white adipose tissue of mammals [J].
Carpéné, C ;
Bousquet-Mélou, A ;
Galitzky, J ;
Berlan, M ;
Lafontan, M .
TRENDS IN COMPARATIVE ENDOCRINOLOGY AND NEUROBIOLOGY: FROM MOLECULAR TO INTEGRATIVE BIOLOGY, 1998, 839 :186-189
[5]   The β-adrenergic receptors and the control of adipose tissue metabolism and thermogenesis [J].
Collins, S ;
Surwit, RS .
RECENT PROGRESS IN HORMONE RESEARCH, VOL 56, 2001, 56 :309-328
[6]   Glycerol and nonesterified fatty acid metabolism in human muscle and adipose tissue in vivo [J].
Coppack, SW ;
Persson, M ;
Judd, RL ;
Miles, JM .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1999, 276 (02) :E233-E240
[7]   ADIPOSE-TISSUE METABOLISM IN OBESITY - LIPASE ACTION INVIVO BEFORE AND AFTER A MIXED MEAL [J].
COPPACK, SW ;
EVANS, RD ;
FISHER, RM ;
FRAYN, KN ;
GIBBONS, GF ;
HUMPHREYS, SM ;
KIRK, ML ;
POTTS, JL ;
HOCKADAY, TDR .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1992, 41 (03) :264-272
[8]  
COPPACK SW, 1994, J LIPID RES, V35, P177
[9]  
CRYER PE, 1980, NEW ENGL J MED, V303, P436
[10]  
EISENHOFER G, 1986, CLIN CHEM, V32, P2030