Limitations in the use of [U-13C6]glucose to estimate gluconeogenesis
Author:
Affiliation:
1. Department of Medicine and Biochemistry, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106-4951
Publisher
American Physiological Society
Subject
Physiology (medical),Physiology,Endocrinology, Diabetes and Metabolism
Link
https://www.physiology.org/doi/pdf/10.1152/ajpendo.1999.277.3.E408
Reference29 articles.
1. Limitations in the Use of [2-14C]Acetate for Measuring Gluconeogenesis In Vivo
2. Determination of Krebs cycle metabolic carbon exchange in vivo and its use to estimate the individual contributions of gluconeogenesis and glycogenolysis to overall glucose output in man.
3. Contributions by kidney and liver to glucose production in the postabsorptive state and after 60 h of fasting.
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2. Regulation of hepatic glucose production and the role of gluconeogenesis in humans: is the rate of gluconeogenesis constant?;Diabetes/Metabolism Research and Reviews;2008-09
3. Glucose metabolism during lactation in a fasting animal, the northern elephant seal;American Journal of Physiology-Regulatory, Integrative and Comparative Physiology;2006-10
4. Peroxisome Proliferator-activated Receptor α (PPARα) Influences Substrate Utilization for Hepatic Glucose Production;Journal of Biological Chemistry;2002-12
5. Underestimation of gluconeogenesis by the [U-13C6]glucose method: effect of lack of isotope equilibrium;American Journal of Physiology-Endocrinology and Metabolism;2002-02-01
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