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  1. AU="Kanta, Josephine M"
  2. AU="Hatfield, Disa L"
  3. AU="Kalima, Pota"
  4. AU="Charisi, Martha"
  5. AU="Carrie L. Byington"
  6. AU="Weakland, Leo F"
  7. AU="Johannes Müller"
  8. AU="Yu, Jieh-Juen"

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Artikel ; Online: Dietary medium-chain fatty acids reduce food intake via the GDF15-GFRAL axis in mice.

Kanta, Josephine M / Deisen, Luisa / Johann, Kornelia / Holm, Stephanie / Lundsgaard, Annemarie / Lund, Jens / Jähnert, Markus / Schürmann, Annette / Clemmensen, Christoffer / Kiens, Bente / Fritzen, Andreas M / Kleinert, Maximilian

Molecular metabolism

2023  Band 74, Seite(n) 101760

Abstract: Objective: Medium chain fatty acids (MCFAs), which are fatty acids with chain lengths of 8-12 carbon atoms, have been shown to reduce food intake in rodents and humans, but the underlying mechanisms are unknown. Unlike most other fatty acids, MCFAs are ... ...

Abstract Objective: Medium chain fatty acids (MCFAs), which are fatty acids with chain lengths of 8-12 carbon atoms, have been shown to reduce food intake in rodents and humans, but the underlying mechanisms are unknown. Unlike most other fatty acids, MCFAs are absorbed from the intestine into the portal vein and enter first the liver. We thus hypothesized that MCFAs trigger the release of hepatic factors that reduce appetite.
Methods: The liver transcriptome in mice that were orally administered MCFAs as C8:0 triacylglycerol (TG) was analyzed. Circulating growth/differentiation factor 15 (GDF15), tissue Gdf15 mRNA and food intake were investigated after acute oral gavage of MCFAs as C8:0 or C10:0 TG in mice. Effects of acute and subchronic administration of MCFAs as C8:0 TG on food intake and body weight were determined in mice lacking either the receptor for GDF15, GDNF Family Receptor Alpha Like (GFRAL), or GDF15.
Results: Hepatic and small intestinal expression of Gdf15 and circulating GDF15 increased after ingestion of MCFAs, while intake of typical dietary long-chain fatty acids (LCFAs) had no effect. Plasma GDF15 levels also increased in the portal vein with MCFA intake, indicating that in addition to the liver, the small intestine contributes to the rise in circulating GDF15. Acute oral provision of MCFAs decreased food intake over 24 h compared with a LCFA-containing bolus, and this anorectic effect required the GDF15 receptor, GFRAL. Moreover, subchronic oral administration of MCFAs reduced body weight over 7 days, an effect that was blunted in mice lacking either GDF15 or GFRAL.
Conclusions: We have identified ingestion of MCFAs as a novel nutritional approach that increases circulating GDF15 in mice and have revealed that the GDF15-GFRAL axis is required for the full anorectic effect of MCFAs.
Mesh-Begriff(e) Humans ; Mice ; Animals ; Appetite Depressants/pharmacology ; Glial Cell Line-Derived Neurotrophic Factor/pharmacology ; Body Weight ; Fatty Acids/metabolism ; Diet, High-Fat ; Triglycerides ; Eating ; Growth Differentiation Factor 15/genetics ; Growth Differentiation Factor 15/metabolism
Chemische Substanzen Appetite Depressants ; Glial Cell Line-Derived Neurotrophic Factor ; Fatty Acids ; Triglycerides ; GDF15 protein, human ; Growth Differentiation Factor 15
Sprache Englisch
Erscheinungsdatum 2023-06-24
Erscheinungsland Germany
Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 2708735-9
ISSN 2212-8778 ; 2212-8778
ISSN (online) 2212-8778
ISSN 2212-8778
DOI 10.1016/j.molmet.2023.101760
Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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