Application of Isotopic Techniques Using Constant Specific Activity or Enrichment to the Study of Carbohydrate Metabolism
Open accessAbstract
Tracer techniques have become an establishedpart of metabolic research and indeed are afundamental part of our understanding of carbo-hydrate metabolism in humans. This review is meant to provide a basic overview of the problems and potential pitfalls associated with these techniques in the hope that they are reliably applied to newer areas of research. A quantitative measurement of the substrate fluxes that determine fasting or postprandial glucose concentrations is central to the determination of the pathophysiology of disease states and of measuring the effect of therapeutic interventions on the disease state. During the fasting state, glucose concentrations are dependent on the rate of endogenous glucose production (EGP) relative to the rate of glucose disappearance; measurement using tracer tech-niques is quite straightforward. The situation is more complex in the postprandial state, where gastric emptying,
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Tracee infusion that mimics glucose appearance in blood to maintain a constant tracer-to-tracee ratio ensures accurate measures of glucose fluxes.
“Tracee infusion that mimics glucose appearance in blood to maintain a constant tracer-to-tracee ratio ensures accurate measures of glucose fluxes [24].”
From Modeling the effect of glucagon on endogenous glucose production in healthy individuals under meal-like conditions (2025) · cites this paper as [24]
The sections “Measurement of glucose turnover using a clamp” and “Glucose turnover in meal studies: triple-tracer methodology” (page numbers unavailable) say that maintaining a relatively constant tracer-to-tracee ratio enables accurate glucose-turnover measurements. But the infusion adjusted to mimic glucose appearance is a tracer infusion, not a tracee infusion as the claim states. (LLM, conf=0.86)
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References 42 · Cited by 67
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- Authors
- Vella, A., & Rizza, R. A.
- Affiliations
- Mayo Clinic (US)
- Corresponding author
- Vella, Adrian
- ORCID
- Vella, Adrian
- Venue
- Diabetes
- Publisher
- American Diabetes Association
- Published
- 2009-10-01
- Volume
- 58
- Issue
- 10
- Pages
- 2168-2174
- ISSN
- 0012-1797 (ISSN-L)
- 1939-327X
- PMC
- PMC2750215
- OpenAlex
- W2102006343
- Cited by
- 67
- References
- 42
- Citations by year
- 2025: 5 · 2024: 1 · 2023: 4 · 2022: 6 · 2021: 3 · 2020: 1 · 2019: 5 · 2018: 12 · 2017: 2 · 2016: 7 · 2015: 6 · 2014: 7 · 2013: 3 · 2012: 3
- FWCI
- 1.21
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Diabetes (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- Mayo Clinic (UL1 RR024150, RR024150)
- Università degli Studi di Padova
- National Institutes of Health (RR024150, UL1-RR-024150-01, RR024150-01)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK029953, DK 29953, R01DK082396, DK078646, R37DK029953, R01DK078646)
- National Center for Research Resources (RR-024150, RR‐024150‐01, UL1RR024150)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Keywords
- isotope tracers, carbohydrate metabolism, tracer techniques, endogenous glucose production, glucose disappearance, postprandial blood glucose, fasting blood glucose, gastric emptying
- MeSH terms
- Blood Glucose, Carbohydrates, Dietary Carbohydrates, Glucose, Humans, Infusions, Intravenous, Isotope Labeling, Isotopes, Kinetics, Models, Biological, Neutrons, Radioisotopes, Scintillation Counting, Sensitivity and Specificity, Splanchnic Circulation
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