GLUCOSE ISOTOPE, CARBON RECYCLING, AND GLUCONEOGENESIS USING [U-C-13]GLUCOSE AND MASS ISOTOPOMER ANALYSIS

被引:23
作者
LEE, WNP
SOROU, S
BERGNER, EA
机构
[1] Department of Pediatrics, Harbor-UCLA Medical Center, Torrance, CA 90509
来源
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY | 1991年 / 45卷 / 03期
关键词
D O I
10.1016/0885-4505(91)90034-I
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
Experimental determinations of glucose carbon recycling using 14C or 13C glucose tracer often underestimate true Cori cycle activity because of dilution and exchange of isotope tracer through the tricarboxylic acid (TCA) cycle. The term glucose isotope recycling therefore is used to distinguish recycling of isotope from recycling of glucose carbon, the actual quantity of circulating glucose recycled. Recently, per-labeled glucose ([U-13C6]glucose) has been used to estimate glucose appearance rate and glucose isotope recycling. Chemical structural information determined by mass isotopomer analysis has been used to correct for dilution of isotope through the TCA cycle. In this report, we present experiments in the study of glucose turnover and recycling using [U-13C6]glucose. Methods of single injection and continuous infusion of [U-13C]glucose are compared. A formula for the calculation of a dilution factor using TCA cycle parameters is derived. In this study of six rabbits, glucose turnover rate ranged from 3.4 to 8.8 mg/kg/min, and glucose m + 3 mass isotopomer recycling from 7 to 12%. The rate of pyruvate carboxylation (Y) was comparable to that of citrate synthetase, having an average relative flux of 0.89. Applying the correction factor for tracer dilution to the observed mass isotopomer recycling, we determined glucose carbon recycling (or Cori cycle activity) to be 22-35% of hepatic glucose output. © 1991.
引用
收藏
页码:298 / 309
页数:12
相关论文
共 17 条
[1]   MEASUREMENT OF TRUE GLUCOSE PRODUCTION-RATES IN INFANCY AND CHILDHOOD WITH 6,6-DIDEUTEROGLUCOSE [J].
BIER, DM ;
LEAKE, RD ;
HAYMOND, MW ;
ARNOLD, KJ ;
GRUENKE, LD ;
SPERLING, MA ;
KIPNIS, DM .
DIABETES, 1977, 26 (11) :1016-1023
[2]   LEAST SQUARES ANALYSIS AND SIMPLIFICATION OF MULTI-ISOTOPE MASS SPECTRA [J].
BRAUMAN, JI .
ANALYTICAL CHEMISTRY, 1966, 38 (04) :607-&
[3]   MODELS TO INTERPRET KINETIC DATA IN STABLE ISOTOPE TRACER STUDIES [J].
COBELLI, C ;
TOFFOLO, G ;
BIER, DM ;
NOSADINI, R .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (05) :E551-E564
[4]   GLUCOSE CARBON RECYCLING AND OXIDATION IN HUMAN NEWBORNS [J].
DENNE, SC ;
KALHAN, SC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (01) :E71-E77
[5]   HEPATIC CARBON FLUX AFTER REFEEDING IN THE GLYCOGEN-STORAGE-DISEASE (GSD GSD) RAT [J].
HOLNESS, MJ ;
PALMER, TN ;
WORRALL, EB ;
SUGDEN, MC .
BIOCHEMICAL JOURNAL, 1987, 248 (03) :969-972
[6]   METABOLIC PATHWAYS LEADING TO LIVER-GLYCOGEN REPLETION INVIVO, STUDIED BY GC-MS AND NMR [J].
KALDERON, B ;
GOPHER, A ;
LAPIDOT, A .
FEBS LETTERS, 1986, 204 (01) :29-32
[7]   GLUCOSE RECYCLING AND PRODUCTION IN GLYCOGENOSIS TYPE-I AND TYPE-III - STABLE ISOTOPE TECHNIQUE STUDY [J].
KALDERON, B ;
KORMAN, SH ;
GUTMAN, A ;
LAPIDOT, A .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (03) :E346-E353
[8]   ESTIMATION OF GLUCOSE-TURNOVER AND C-13 RECYCLING IN THE HUMAN NEWBORN BY SIMULTANEOUS [1-C-13-LABELED] GLUCOSE AND [6,6-H-2(2)]-LABELED GLUCOSE TRACERS [J].
KALHAN, SC ;
BIER, DM ;
SAVIN, SM ;
ADAM, PAJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1980, 50 (03) :456-460
[9]   DETERMINATION OF SYNTHESIS, RECYCLING AND BODY MASS OF GLUCOSE IN RATS AND RABBITS INVIVO WITH H-3-LABELED AND C-14-LABELED GLUCOSE [J].
KATZ, J ;
DUNN, A ;
CHENOWETH, M ;
GOLDEN, S .
BIOCHEMICAL JOURNAL, 1974, 142 (01) :171-183
[10]  
KATZ J, 1989, J BIOL CHEM, V264, P12994