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Palmitate-mediated induction of neuropeptide Y expression occurs through intracellular metabolites and not direct exposure to proinflammatory cytokines.
- Source :
-
Journal of neurochemistry [J Neurochem] 2021 Nov; Vol. 159 (3), pp. 574-589. Date of Electronic Publication: 2021 Sep 20. - Publication Year :
- 2021
-
Abstract
- A contributing factor to the development of obesity is the consumption of a diet high in saturated fatty acids, such as palmitate. These fats induce hypothalamic neuroinflammation, which dysregulates neuronal function and induces orexigenic neuropeptide Y (Npy) to promote food intake. An inflammatory cytokine array identified multiple candidates that could mediate palmitate-induced up-regulation of Npy mRNA levels. Of these, visfatin or nicotinamide phosphoribosyltransferase (NAMPT), macrophage migratory inhibitory factor (MIF), and IL-17F were chosen for further study. Direct treatment of the neuropeptide Y/agouti-related peptide (NPY/AgRP)-expressing mHypoE-46 neuronal cell line with the aforementioned cytokines demonstrated that visfatin could directly induce Npy mRNA expression. Preventing the intracellular metabolism of palmitate through long-chain acyl-CoA synthetase (ACSL) inhibition was sufficient to block the palmitate-mediated increase in Npy gene expression. Furthermore, thin-layer chromatography revealed that in neurons, palmitate is readily incorporated into ceramides and defined species of phospholipids. Exogenous C16 ceramide, dipalmitoyl-phosphatidylcholine, and dipalmitoyl-phosphatidylethanolamine were sufficient to significantly induce Npy expression. This study suggests that the intracellular metabolism of palmitate and elevation of metabolites, including ceramide and phospholipids, are responsible for the palmitate-mediated induction of the potent orexigen Npy. Furthermore, this suggests that the regulation of Npy expression is less reliant on inflammatory cytokines per se than palmitate metabolites in a model of NPY/AgRP neurons. These lipid species likely induce detrimental downstream cellular signaling events ultimately causing an increase in feeding, resulting in an overweight phenotype and/or obesity.<br /> (© 2021 International Society for Neurochemistry.)
- Subjects :
- Acyl Coenzyme A metabolism
Animals
Cell Line
Ceramides metabolism
Culture Media, Conditioned
Diet, High-Fat
Gene Expression drug effects
Male
Mice
Mice, Inbred C57BL
Neurons metabolism
Nicotinamide Phosphoribosyltransferase pharmacology
RNA, Messenger biosynthesis
RNA, Messenger genetics
Cytokines pharmacology
Neuropeptide Y biosynthesis
Palmitates pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1471-4159
- Volume :
- 159
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of neurochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 34482548
- Full Text :
- https://doi.org/10.1111/jnc.15504