Gluconeogenesis and the Cori cycle in 12-, 20-, and 40-h-fasted humans

被引:81
作者
Katz, J [1 ]
Tayek, JA [1 ]
机构
[1] Univ Calif Los Angeles, Harbor Med Ctr, Dept Internal Med, Torrance, CA 90502 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1998年 / 275卷 / 03期
关键词
glucose production; glucose recycling; free fatty acids; insulin; glycogenolysis; glycogen;
D O I
10.1152/ajpendo.1998.275.3.E537
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Six subjects were infused with [U-C-13]glucose (0.03-0.05 mg kg-l min-l) starting 8-9 h after a meal, and the production of glucose, the recycling of glucose (the Cori cycle), the dilution of glucose by unlabeled carbon into the hepatic lactate-pyruvate pool, and gluconeogenesis were determined in these fasted volunteers by use of mass isotopomer analysis and equations previously described [J. A. Tayek and J. Katz. Am. J. Physiol. 272 (Endocrinol. Metab. 35): E476-E484, 1997]. A primed continuous Il-h infusion was started at 6:00 AM, and the above parameters were calculated after 3 h (for the 12-h fast) and at the end of the infusion (for the 20-h fast). Another group of five subjects was fasted for 40 h, and the above parameters were calculated as before. At 12, 20, and 40 h of fasting, respectively, blood glucose was 93 +/- 2, 83 +/- 2, and 71 +/- 2 (SE) mg/dl; glucose production was 2.3, 1.8, and 1.77 mg . kg(-1) min(-1); the recycling of labeled carbon was 8, 15, and 15%, and that of glucose molecules (Cori cycle) was 18, 35, and 36%; the contribution of gluconeogenesis to glucose production was 41, 71, and 92% or 0.96, 1.29, and 1.64 mg . kg(-1) . min(-1); and the contribution of other sources to glucose production was 1.37, 0.53, and 0.15 mg kg(-1) . min(-1). The recycling of glucose is important in prolonged fasting for the maintenance of plasma glucose concentration. We demonstrate here that gluconeogenesis can be easily measured and that it accounts for similar to 90% of glucose production after a 40-h fast.
引用
收藏
页码:E537 / E542
页数:6
相关论文
共 26 条
  • [1] GLYCOGEN TURNOVER DURING REFEEDING IN THE POSTABSORPTIVE DOG - IMPLICATIONS FOR THE ESTIMATION OF GLYCOGEN FORMATION USING TRACER METHODS
    BARRETT, EJ
    BEVILACQUA, S
    DEFRONZO, RA
    FERRANNINI, E
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1994, 43 (03): : 285 - 292
  • [2] Quantifying gluconeogenesis during fasting
    Chandramouli, V
    Ekberg, K
    Schumann, WC
    Kalhan, SC
    Wahren, J
    Landau, BR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 273 (06): : E1209 - E1215
  • [3] CLINE GL, 1994, J CLIN INVEST, P269
  • [4] CORI LF, 1981, CURRENT TOPICS CELL, V5, P372
  • [5] SIMULTANEOUS SYNTHESIS AND DEGRADATION OF RAT-LIVER GLYCOGEN - AN INVIVO NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPIC STUDY
    DAVID, M
    PETIT, WA
    LAUGHLIN, MR
    SHULMAN, RG
    KING, JE
    BARRETT, EJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (02) : 612 - 617
  • [6] HELLERSTEIN M, 1995, DIABETES S, V44, P153
  • [7] Hepatic gluconeogenic fluxes and glycogen turnover during fasting in humans - A stable isotope study
    Hellerstein, MK
    Neese, RA
    Linfoot, P
    Christiansen, M
    Turner, S
    Letscher, A
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (05) : 1305 - 1319
  • [8] KALDERON B, 1989, AM J PHYSIOL, V257, P346
  • [9] Contributions of gluconeogenesis to glucose production in the fasted state
    Landau, BR
    Wahren, J
    Chandramouli, V
    Schumann, WC
    Ekberg, K
    Kalhan, SC
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (02) : 378 - 385
  • [10] LEE WP, 1994, CLIN RES, V42, pA28