The dietary regulation of LEAP2 depends on meal composition in mice

Author:

Gradel Anna Katrina Jógvansdóttir123ORCID,Holm Stephanie K.14,Byberg Sarah1,Merkestein Myrte3,Hogendorf Wouter Frederik Johan5,Lund Mari Lilith4,Buijink Jesse Arnold4,Damgaard Jesper3,Lykkesfeldt Jens2,Holst Birgitte1

Affiliation:

1. Department of Biomedical Sciences, Faculty of Health & Medical Sciences University of Copenhagen Copenhagen Denmark

2. Section for Experimental Animal Models, Department of Veterinary and Animal Sciences, Faculty of Health & Medical Sciences University of Copenhagen Copenhagen Denmark

3. Global Drug Discovery Novo Nordisk A/S Måløv Denmark

4. Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health & Medical Sciences University of Copenhagen Copenhagen Denmark

5. Global Research Technologies Novo Nordisk A/S Måløv Denmark

Abstract

AbstractGhrelin represents a key hormone regulating energy balance. Upon activation of the growth hormone secretagogue receptor (GHSR), ghrelin increases blood glucose levels, food intake, and promotes weight gain. The liver‐expressed antimicrobial peptide 2 (LEAP2) acts as an endogenous antagonist of the GHSR. While the regulation of LEAP2 and its effect on the GHSR likely occur in an opposite pattern to that of ghrelin, the dietary regulation of LEAP2 remains to be described. We, therefore, examined the regulation of LEAP2 by different acute meal challenges (glucose, mixed meal, olive, lard, and fish oil) and diets (chow vs. high‐fat) in C57BL/6 male mice. In addition, the effect of specific fatty acids (oleic, docosahexaenoic, and linoleic acid) on LEAP2 was assessed in murine intestinal organoids. While only mixed meal increased liver Leap2 expression, all meal challenges except fish oil increased jejunal Leap2 expression compared to water. Leap2 expression correlated with levels of hepatic glycogen and jejunal lipids. Lipid versus water dosing increased LEAP2 levels in the systemic circulation and portal vein where fish oil was associated with the smallest increase. In line with this, oleic acid, but not docosahexaenoic acid increased Leap2 expression in intestinal organoids. Feeding mice with high‐fat versus chow diet not only increased plasma LEAP2 levels, but also the increment in plasma LEAP2 upon dosing with olive oil versus water. Taken together, these results show that LEAP2 is regulated by meal ingestion in both the small intestine and the liver according to the meal/diet of interest and local energy stores.

Funder

Novo Nordisk Foundation Center for Basic Metabolic Research

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

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