Splanchnic and Leg Glucagon Metabolism in Healthy Individuals and Those With Type 1 Diabetes: First-in-Human Study Using [13C9,15N1]Glucagon

This study was conducted to assess splanchnic and leg glucagon metabolism in humans using stable glucagon isotopes. We wanted to evaluate whether splanchnic and leg glucagon metabolism differed between participants with no diabetes (ND) and those with type 1 diabetes (T1D) at glucagon concentrations spanning the physiological range. Whereas splanchnic glucagon extraction did not differ between participants with ND and those with T1D, leg glucagon extraction fell in those with ND but did not change in those with T1D as glucagon concentrations increased. Net splanchnic glucagon production did not change with exogenous glucagon infusion. Our study has implications for dual hormone closed-loop control in T1D where glucagon is infused for prevention of hypoglycemia and for investigating the effects of emerging GLP-1, glucose-dependent insulinotropic polypeptide, and glucagon receptor agonists on endogenous glucagon secretion and clearance.

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Publication Details

Journal
Diabetes
Published
2025-05-30
DOI
https://doi.org/10.2337/db24-1064
Citations
2
Primary Topic
Pancreatic function and diabetes
Type
article
Field-Weighted Citation Impact
4.01

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article

Splanchnic and Leg Glucagon Metabolism in Healthy Individuals and Those With Type 1 Diabetes: First-in-Human Study Using [13C9,15N1]Glucagon

Ananda Basu, Yogesh Yadav, Akhilesh Pandey, Claudio Cobelli et al.
2 citations
Diabetes
Pancreatic function and diabetes
4.01
article

Splanchnic and Leg Glucagon Metabolism in Healthy Individuals and Those With Type 1 Diabetes: First-in-Human Study Using [13C9,15N1]Glucagon

Ananda Basu, Yogesh Yadav, Akhilesh Pandey, Claudio Cobelli, Luke R. Wilkins, Rita Basu, Michele Schiavon, FNU RUCHI, Chiara Dalla Man
article en
2 citations

Abstract

This study was conducted to assess splanchnic and leg glucagon metabolism in humans using stable glucagon isotopes. We wanted to evaluate whether splanchnic and leg glucagon metabolism differed between participants with no diabetes (ND) and those with type 1 diabetes (T1D) at glucagon concentrations spanning the physiological range. Whereas splanchnic glucagon extraction did not differ between participants with ND and those with T1D, leg glucagon extraction fell in those with ND but did not change in those with T1D as glucagon concentrations increased. Net splanchnic glucagon production did not change with exogenous glucagon infusion. Our study has implications for dual hormone closed-loop control in T1D where glucagon is infused for prevention of hypoglycemia and for investigating the effects of emerging GLP-1, glucose-dependent insulinotropic polypeptide, and glucagon receptor agonists on endogenous glucagon secretion and clearance.

DiabetesVol. 74(8)
Mayo Clinic (US), University of Padua (IT), University of Alabama at Birmingham (US), Mayo Clinic in Arizona (US), Mayo Clinic in Florida (US), University of Virginia (US)
Vanderbilt University, Vanderbilt University Medical Center, National Institutes of Health, Division of Diabetes, Endocrinology, and Metabolic Diseases
Good health and well-being
Openalex Percentile: Top 7%
Pancreatic function and diabetes
4.01
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