Fatty Acid Metabolites as Novel Regulators of Non-shivering Thermogenesis.

Brite adipocytes Brown adipocytes Endocannabinoids Oxylipins PUFAs Thermogenesis Ucp1 ω-3 ω-6

Journal

Handbook of experimental pharmacology
ISSN: 0171-2004
Titre abrégé: Handb Exp Pharmacol
Pays: Germany
ID NLM: 7902231

Informations de publication

Date de publication:
2019
Historique:
pubmed: 25 8 2018
medline: 19 7 2019
entrez: 25 8 2018
Statut: ppublish

Résumé

Fatty acids are essential contributors to adipocyte-based non-shivering thermogenesis by acting as activators of uncoupling protein 1 and serving as fuel for mitochondrial heat production. Novel evidence suggests a contribution to this thermogenic mechanism by their conversion to bioactive compounds. Mammalian cells produce a plethora of oxylipins and endocannabinoids, some of which have been identified to affect the abundance or thermogenic activity of brown and brite adipocytes. These effectors are produced locally or at distant sites and signal toward thermogenic adipocytes via a direct interaction with these cells or indirectly via secondary mechanisms. These interactions are evoked by the activation of receptor-mediated pathways. The endogenous production of these compounds is prone to modulation by the dietary intake of the respective precursor fatty acids. The effect of nutritional interventions on uncoupling protein 1-derived thermogenesis may thus at least in part be conferred by the production of a supportive oxylipin and endocannabinoid profile. The manipulation of this system in future studies will help to elucidate the physiological potential of these compounds as novel, endogenous regulators of non-shivering thermogenesis.

Identifiants

pubmed: 30141101
doi: 10.1007/164_2018_150
doi:

Substances chimiques

Fatty Acids 0
Uncoupling Protein 1 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

183-214

Auteurs

Stefanie F Maurer (SF)

Molecular Nutritional Medicine, Else Kröner-Fresenius Center for Nutritional Medicine, Technical University of Munich, Freising, Germany. stefanie.maurer@tum.de.
ZIEL Institute for Food and Health, TUM School of Life Sciences, Technical University of Munich, Freising, Germany. stefanie.maurer@tum.de.

Sebastian Dieckmann (S)

Molecular Nutritional Medicine, Else Kröner-Fresenius Center for Nutritional Medicine, Technical University of Munich, Freising, Germany.
ZIEL Institute for Food and Health, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.

Karin Kleigrewe (K)

Bavarian Center for Biomolecular Mass Spectrometry (BayBioMS), Technical University of Munich, Freising, Germany.

Cécilia Colson (C)

Université Côte d'Azur, CNRS, Inserm, iBV, Nice, France.

Ez-Zoubir Amri (EZ)

Université Côte d'Azur, CNRS, Inserm, iBV, Nice, France.

Martin Klingenspor (M)

Molecular Nutritional Medicine, Else Kröner-Fresenius Center for Nutritional Medicine, Technical University of Munich, Freising, Germany.
ZIEL Institute for Food and Health, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.

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Classifications MeSH