Insulin secretion and action and the response of endogenous glucose production to a lack of glucagon suppression in nondiabetic subjects
Open accessAbstract
In prediabetes, anthropometric characteristics as well as insulin action do not alter the hepatic response to glucagon. The postprandial suppression or lack of suppression of glucagon secretion is an important factor governing postprandial glucose tolerance independent of insulin secretion.
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An experiment like the ideal glucagon-isolation experiment was performed in a prior study to examine the effect of impaired glucagon suppression on glucose at different degrees of insulin secretory impairment.
“An experiment like this was performed in [16] with the purpose of examining the effect of impaired glucagon suppression on glucose at different degrees of insulin secretory impairment.”
From Modeling the effect of glucagon on endogenous glucose production in healthy individuals under meal-like conditions (2025) · cites this paper as [16]
In the prior experiment, estimated endogenous glucose production profiles showed that the glucagon stimulatory effect on endogenous glucose production is not constant but wanes after a few hours.
“There, the estimated EGP profiles clearly showed that the glucagon stimulatory effect on EGP is not constant but wanes after a few hours.”
From Modeling the effect of glucagon on endogenous glucose production in healthy individuals under meal-like conditions (2025) · cites this paper as [16]
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Self-citation
- Authors
- Adams, J. D., Egan, A. M., Laurenti, M. C., Schembri Wismayer, D., Bailey, K. R., Cobelli, C., Dalla Man, C., & Vella, A.
- Affiliations
- Mayo Clinic (US)
- Division of Endocrinology, Diabetes & Metabolism, Mayo Clinic College of Medicine, Rochester, Minnesota
- University of Padua (IT)
- Department of Information Engineering, University of Padova, Padova, Italy
- Corresponding author
- Vella, Adrian
- ORCID
- Venue
- American Journal of Physiology-Endocrinology and Metabolism
- Publisher
- American Physiological Society
- Published
- 2021-11-01
- Volume
- 321
- Issue
- 5
- Pages
- E728-E736
- ISSN
- 0193-1849 (ISSN-L)
- 1522-1555
- PMC
- PMC8782666
- OpenAlex
- W3206412396
- Cited by
- 10
- References
- 32
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 3 · 2023: 2 · 2022: 2
- FWCI
- 1.64
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Padua Research Archive (University of Padova) (submittedVersion)
- Funders
- HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (DK78646, DK116231, DK126206)
- Mayo Clinic General Clinical Research Center (DK TR000135)
- Topics
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Keywords
- insulin secretion, insulin action, glucagon, hepatic glucose production, glucagon suppression, prediabetes, non-diabetic patients, anthropometric characteristics
- MeSH terms
- Insulin Secretion, Blood Glucose, Female, Glucagon, Glucose, Glucose Tolerance Test, Humans, Insulin, Islets of Langerhans, Male, Middle Aged, Somatostatin, Postprandial Period, Healthy Volunteers
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