An acute microglial metabolic response controls metabolism and improves memory

Abstract: Chronic high-fat feeding triggers metabolic dysfunction including obesity, insulin resistance, and diabetes. How high-fat intake first triggers these pathophysiological states remains unknown. Here, we identify an acute microglial metabolic response that rapidly translates intake of high-fat diet (HFD) to a surprisingly beneficial effect on metabolism and spatial/learning memory. High-fat intake rapidly increases palmitate levels in cerebrospinal fluid and triggers a wave of microglial metabolic activation characterized by mitochondrial membrane activation and fission as well as metabolic skewing toward aerobic glycolysis. These effects are detectable throughout the brain and can be detected within as little as 12 hr of HFD exposure. In vivo, microglial ablation and conditional DRP1 deletion show that the microglial metabolic response is necessary for the acute effects of HFD. 13C-tracing experiments reveal that in addition to processing via β-oxidation, microglia shunt a substantial fraction of palmitate toward anaplerosis and re-release of bioenergetic carbons into the extracellular milieu in the form of lactate, glutamate, succinate, and intriguingly, the neuroprotective metabolite itaconate. Together, these data identify microglia as a critical nutrient regulatory node in the brain, metabolizing away harmful fatty acids and liberating the same carbons as alternate bioenergetic and protective substrates for surrounding cells. The data identify a surprisingly beneficial effect of short-term HFD on learning and memory

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch
Notes
eLife. - 12 (2024) , RP87120, ISSN: 2050-084X

Event
Veröffentlichung
(where)
Freiburg
(who)
Universität
(when)
2024
Creator
Drougard, Anne
Ma, Eric H.
Wegert, Vanessa
Sheldon, Ryan
Panzeri, Ilaria
Vatsa, Naman
Apostle, Stefanos
Fagnocchi, Luca
Schaf, Judith
Gossens, Klaus
Völker, Josephine
Pang, Shengru
Bremser, Anna
Dror, Erez
Giacona, Francesca
Sagar
Henderson, Michael X.
Prinz, Marco
Jones, Russell G.
Pospisilik, J. Andrew

DOI
10.7554/elife.87120
URN
urn:nbn:de:bsz:25-freidok-2605501
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:30 AM CEST

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Associated

Time of origin

  • 2024

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