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Alexander Hovard Sparre-Ulrich

Researcher at University of Copenhagen

Publications -  30
Citations -  1607

Alexander Hovard Sparre-Ulrich is an academic researcher from University of Copenhagen. The author has contributed to research in topics: Receptor & Chemokine receptor. The author has an hindex of 16, co-authored 25 publications receiving 1271 citations.

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Journal ArticleDOI

Separate and Combined Glucometabolic Effects of Endogenous Glucose-Dependent Insulinotropic Polypeptide and Glucagon-like Peptide 1 in Healthy Individuals.

TL;DR: Examining the individual and combined contributions of endogenous GIP and GLP-1 to the postprandial changes in glucose and glucoregulatory hormones using the novel GIP receptor antagonist GIP(3-30)NH2 and the well-established GLp-1 receptor antagonist exendin(9-39) NH2 found that A and C resulted in higher glucagon levels and faster gastric emptying.
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The Gluco- and Liporegulatory and Vasodilatory Effects of Glucose-Dependent Insulinotropic Polypeptide (GIP) Are Abolished by an Antagonist of the Human GIP Receptor

TL;DR: The changes in glucose infusion rates and plasma insulin levels demonstrate an inhibitory effect of the antagonist on the incretin effect of GIP, indicating that GIP also plays a crucial role in lipid metabolism.
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N‐terminally and C‐terminally truncated forms of glucose‐dependent insulinotropic polypeptide are high‐affinity competitive antagonists of the human GIP receptor

TL;DR: Eight N‐terminal truncations of human GIP(1–30)NH2 are characterized and high‐affinity ligands for the GIP receptor are needed to elucidate the physiological functions and pharmacological potential of GIP in vivo.
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Species-specific action of (Pro3)GIP – a full agonist at human GIP receptors, but a partial agonist and competitive antagonist at rat and mouse GIP receptors

TL;DR: In this paper, a pharmacological analysis of (Pro3)GIP including interspecies differences between the rodent and human GIP system was conducted, and it was shown that Rodent GIPs are more potent and efficacious at their receptors than humanGIPs.