Glucose-Dependent Insulinotropic Polypeptide Is Involved in Postprandial Regulation of Splanchnic Blood Supply

Administration of the gut hormone glucose-dependent insulinotropic polypeptide (GIP) increases splanchnic blood flow. We investigated the role of endogenous GIP in splanchnic blood flow regulation using a receptor antagonist in humans. Oral glucose ingestion increased blood flow in the superior mesenteric artery by ∼70%, and the increase was significantly lower during concurrent infusion of the GIP receptor antagonist. Thus, endogenous GIP contributed ∼22% of the postprandial increase in superior mesenteric artery blood flow. We have identified a novel physiological aspect of vascular biology related to the GIP receptor in humans. Treatments targeting the GIP receptors are likely to affect splanchnic blood flow.

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Publication Details

Journal
Diabetes
Published
2025-05-30
DOI
https://doi.org/10.2337/db25-0149
Citations
3
Primary Topic
Cardiovascular Function and Risk Factors
Type
article
Field-Weighted Citation Impact
4.16

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article

Glucose-Dependent Insulinotropic Polypeptide Is Involved in Postprandial Regulation of Splanchnic Blood Supply

Kirsa Skov‐Jeppesen, Henrik Larsson, METTE MARIE ROSENKILDE, Lærke S. Gasbjerg et al.
3 citations
Diabetes
Cardiovascular Function and Risk Factors
4.16
article

Glucose-Dependent Insulinotropic Polypeptide Is Involved in Postprandial Regulation of Splanchnic Blood Supply

Kirsa Skov‐Jeppesen, Henrik Larsson, METTE MARIE ROSENKILDE, Lærke S. Gasbjerg, Bolette Hartmann, Ulrik B. Andersen, Bryan Haddock, Rasmus Syberg Rasmussen, Sophie W. Nielsen, Ali Asmar, Jens Juul Holst, Helle Hjorth Johannesen, Mark Bitsch Vestergaard, Frederikke Østergaard, Ludvig S. Langberg
article en
3 citations

Abstract

Administration of the gut hormone glucose-dependent insulinotropic polypeptide (GIP) increases splanchnic blood flow. We investigated the role of endogenous GIP in splanchnic blood flow regulation using a receptor antagonist in humans. Oral glucose ingestion increased blood flow in the superior mesenteric artery by ∼70%, and the increase was significantly lower during concurrent infusion of the GIP receptor antagonist. Thus, endogenous GIP contributed ∼22% of the postprandial increase in superior mesenteric artery blood flow. We have identified a novel physiological aspect of vascular biology related to the GIP receptor in humans. Treatments targeting the GIP receptors are likely to affect splanchnic blood flow.

DiabetesVol. 74(8)
University of Copenhagen (DK), Novo Nordisk Foundation (DK), Frederiksberg Hospital (DK), Glostrup Hospital (DK), Copenhagen University Hospital (DK), Rigshospitalet (DK), University College Copenhagen (DK), IT University of Copenhagen (DK)
Hørslev-Fonden, Den A. P. Møllerske Støttefond, European Foundation for the Study of Diabetes, Novo Nordisk, Rigshospitalet, Region Hovedstaden, Kong Christian den Tiendes Fond, Novo Nordisk Fonden
Good health and well-being
Openalex Percentile: Top 6%
Cardiovascular Function and Risk Factors
4.16
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