High-fat diet consumption alters energy metabolism in the mouse hypothalamus

Background/Objectives High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The sp...

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Published inInternational Journal of Obesity Vol. 43; no. 6; pp. 1295 - 1304
Main Authors Lizarbe, Blanca, Cherix, Antoine, Duarte, João M. N., Cardinaux, Jean-René, Gruetter, Rolf
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.06.2019
Nature Publishing Group
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Summary:Background/Objectives High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The specific effects of high-fat diet on hypothalamic energy metabolism and neurotransmission are however not yet known and have not been investigated before. Subjects/Methods We used 1 H and 13 C magnetic resonance spectroscopy (MRS) and immunofluorescence techniques to evaluate in vivo the consequences of high-saturated fat diet administration to mice, and explored the effects on hypothalamic metabolism in three mouse cohorts at different time points for up to 4 months. Results We found that high-fat diet increases significantly the hypothalamic levels of glucose ( P  < 0.001), osmolytes ( P  < 0.001), and neurotransmitters ( P  < 0.05) from 2 months of diet, and alters the rates of metabolic ( P  < 0.05) and neurotransmission fluxes ( P  < 0.001), and the contribution of non-glycolytic substrates to hypothalamic metabolism ( P  < 0.05) after 10 weeks of high-fat feeding. Conclusions/interpretation We report changes that reveal a high-fat diet-induced alteration of hypothalamic metabolism and neurotransmission that is quantifiable by 1 H and 13 C MRS in vivo, and present the first evidence of the extension of the inflammation pathology to a localized metabolic imbalance.
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ISSN:0307-0565
1476-5497
1476-5497
DOI:10.1038/s41366-018-0224-9