Comparison of [3,4-13C2]glucose to [6,6-2H2]glucose as a tracer for glucose turnover by nuclear magnetic resonance

被引:19
作者
Jin, ES
Jones, JG
Burgess, SC
Merritt, ME
Sherry, AD
Malloy, CR
机构
[1] Univ Texas, SW Med Ctr, Mary Nell & Ralph B Rogers Magnet Resonance Ctr, Dept Radiol, Dallas, TX 75235 USA
[2] Univ Coimbra, Ctr Neurosci & Cell Biol, P-3000 Coimbra, Portugal
[3] Univ Coimbra, Dept Biochem, P-3000 Coimbra, Portugal
[4] Univ Texas, Dept Chem, Richardson, TX USA
[5] VA N Texas Healthcare Syst, Dallas, TX USA
关键词
stable isotope tracers; C-13; H-2; NMR; glucose turnover;
D O I
10.1002/mrm.20496
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
A recently introduced tracer, [3,4-C-13(2)]glucose, was compared to the widely used tracer, [6,6-H-2(2)]glucose, for measurement of whole-body glucose turnover. The rate of glucose production (GP) was measured in rats after primed infusions of [3,4-(13)C2]glucose, [6,6-(2)H2]glucose, or both tracers simultaneously followed by a constant infusion of tracer(s) over 90 min. Blood glucose was purified and converted into monoacetone glucose for analysis by (CNMR)-C-13 (for [3,4-C-13(2)]glucose) or H-1 and H-2 NMR (for [6,6-(2)H2]glucose). The values of GP measured during infusion of each single tracer were not significantly different. In rats infused with both tracers simultaneously, GP was identical as reported by each tracer, 42 +/- 4 mu mol/kg/min. Since H-2 and C-13 enrichment in glucose is typically much less than 2% for in vivo studies, [3,4-C-13(2)]glucose does not interfere with measurements of C-13 or H-2 enrichment patterns and therefore is valuable when multiple metabolic pathways are being evaluated simultaneously. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:1479 / 1483
页数:5
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