4.6 Article

Use of 2H2O for estimating rates of gluconeogenesis: determination and correction of error due to transaldolase exchange

Journal

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpendo.00306.2012

Keywords

deuterated water; transaldolase; stable isotope; gluconeogenesis; glycogenolysis

Funding

  1. Clinical and Translational Science Award at UT Southwestern [UL1 RR-024982]
  2. Task Force for Obesity Research (TORS) at UT Southwestern [UL1 DE-019584]
  3. TORS Human Biology Core [PL1 DK-081183]
  4. TORS Molecular and Metabolic Mouse Phenotyping Core [PL1 DK-081182]
  5. NIH [RL1 DK-081187, K23 DK-074396, R01 DK-087977, RR-02584, R01 DK-078184]
  6. American Diabetes Association [7-09-BS-24]

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Browning JD, Burgess SC. Use of (H2O)-H-2 for estimating rates of gluconeogenesis: determination and correction of error due to transaldolase exchange. Am J Physiol Endocrinol Metab 303: E1304-E1312, 2012. First published October 17, 2012; doi: 10.1152/ajpendo.00306.2012.-The use of deuterated water as a method to measure gluconeogenesis has previously been well validated and is reflective of normal human physiology. However, there has been concern since the method was first introduced that transaldolase exchange may lead to the overestimation of gluconeogenesis. We examined the impact of transaldolase exchange on the estimation of gluconenogenesis using the deuterated water method under a variety of physiological conditions in humans by using the gluconeogenic tracer [U-C-13] propionate, (H2O)-H-2, and H-2/C-13 nuclear magnetic resonance (NMR) spectroscopy. When [U-C-13] propionate was used, C-13 labeling inequality occurred between the top and bottom halves of glucose in individuals fasted for 12-24 h who were weight stable (n = 18) or had lost weight via calorie restriction (n = 7), consistent with transaldolase exchange. Similar analysis of glucose standards revealed no significant difference in the total C-13 enrichment between the top and bottom halves of glucose, indicating that the differences detected were biological, not analytical, in origin. This labeling inequality was attenuated by extending the fasting period to 48 h (n = 12) as well as by dietary carbohydrate restriction (n = 7), both conditions associated with decreased glycogenolysis. These findings were consistent with a transaldolase effect; however, the resultant overestimation of gluconeogenesis in the overnight-fasted state was modest (7-12%), leading to an error of 14-24% that was easily correctable by using either a simultaneous C-13 gluconeogenic tracer or a correction nomogram generated from data in the present study.

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