Stable isotope-labeled tracers for the investigation of fatty acid and triglyceride metabolism in humans in vivo

被引:37
作者
Magkos, Faidon [1 ,2 ]
Mittendorfer, Bettina [1 ]
机构
[1] Washington Univ, Sch Med, Div Geriatr & Nutr Sci, St Louis, MO 63110 USA
[2] Harokopio Univ, Dept Nutr & Dietet, Athens, Greece
关键词
adipose tissue; lipid metabolism; lipolysis; lipoprotein; liver; mass spectrometry; oxidation; LOW-DENSITY LIPOPROTEIN; HUMAN SKELETAL-MUSCLE; DE-NOVO LIPOGENESIS; SUBCUTANEOUS ADIPOSE-TISSUE; VLDL-TRIGLYCERIDE; PLASMA TRIGLYCERIDE; APOLIPOPROTEIN B-100; LIPID-METABOLISM; DIETARY-FAT; WHOLE-BODY;
D O I
10.2217/CLP.09.9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Understanding lipid metabolism and its regulation requires information concerning the rates at which lipids are produced within the body, absorbed (dietary lipids) into the body, transported within the body, and utilized by various tissues. This article focuses on the use of stable isotope-labeled tracers for the quantitative evaluation of major pathways of fatty acid and triglyceride metabolism in humans in vivo. Adipose tissue lipolysis and free fatty acid appearance in plasma, fatty acid tissue uptake and oxidation, and hepatic VLDL triglyceride secretion are among the metabolic pathways that can be studied by using stable isotope-labeled tracers, and will be discussed in detail. The methodology has been in use for many years and is constantly being refined. A variety of tracers and analytical approaches are available and can be used; knowing the advantages, assumptions and limitations of each is essential for the planning of studies and the interpretation of data, which may provide unique insights into human lipid metabolism.
引用
收藏
页码:215 / 230
页数:16
相关论文
共 128 条
[1]   Contributions of de novo synthesis of fatty acids to total VLDL-triglyceride secretion during prolonged hyperglycemia hyperinsulinemia in normal man [J].
Aarsland, A ;
Chinkes, D ;
Wolfe, RR .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (09) :2008-2017
[2]   Acute suppression of VLDL1 secretion rate by insulin is associated with hepatic fat content and insulin resistance [J].
Adiels, M. ;
Westerbacka, J. ;
Soro-Paavonen, A. ;
Haekkinen, A. M. ;
Vehkavaara, S. ;
Caslake, M. J. ;
Packard, C. ;
Olofsson, S. O. ;
Yki-Jaervinen, H. ;
Taskinen, M. R. ;
Boren, J. .
DIABETOLOGIA, 2007, 50 (11) :2356-2365
[3]   A new combined multicompartmental model for apolipoprotein B-100 and triglyceride metabolism in VLDL subfractions [J].
Adiels, M ;
Packard, C ;
Caslake, MJ ;
Stewart, P ;
Soro, A ;
Westerbacka, J ;
Wennberg, B ;
Olofsson, SO ;
Taskinen, MR ;
Borén, J .
JOURNAL OF LIPID RESEARCH, 2005, 46 (01) :58-67
[4]   Development of a novel method to determine very low density lipoprotein kinetics [J].
Al-Shayji, Iqbal A. R. ;
Gill, Jason M. R. ;
Cooney, Josephine ;
Siddiqui, Samira ;
Caslake, Muriel J. .
JOURNAL OF LIPID RESEARCH, 2007, 48 (09) :2086-2095
[5]   TRACER PRIMING BICARBONATE POOL [J].
ALLSOP, JR ;
WOLFE, RR ;
BURKE, JF .
JOURNAL OF APPLIED PHYSIOLOGY, 1978, 45 (01) :137-139
[6]   REGULATION OF PLASMA FREE FATTY ACID TURNOVER [J].
ARMSTRONG, D ;
STEELE, R ;
DEBODO, RC ;
DUNN, A ;
BISHOP, JS ;
ALTSZULER, N .
AMERICAN JOURNAL OF PHYSIOLOGY, 1961, 201 (01) :9-&
[7]   Human fat cell lipolysis: Biochemistry, regulation and clinical role [J].
Arner, P .
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 19 (04) :471-482
[8]   Contributions of different fatty acid sources to very low-density lipoprotein-triacylglycerol in the fasted and fed states [J].
Barrows, BR ;
Parks, EJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (04) :1446-1452
[9]  
BARTER PJ, 1972, J LIPID RES, V13, P483
[10]  
Betteridge DJ., 1999, LIPOPROTEINS HLTH DI