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Xiphoid nucleus of the midline thalamus controls cold-induced food seeking.

Nature · 2023 · Vol. 621 (7977) · pp. 138-145

Abstract

Maintaining body temperature is calorically expensive for endothermic animals<sup>1</sup>. Mammals eat more in the cold to compensate for energy expenditure<sup>2</sup>, but the neural mechanism underlying this coupling is not well understood. Through behavioural and metabolic analyses, we found that mice dynamically switch between energy-conservation and food-seeking states in the cold, the latter of which are primarily driven by energy expenditure rather than the sensation of cold. To identify the neural mechanisms underlying cold-induced food seeking, we used whole-brain c-Fos mapping and found that the xiphoid (Xi), a small nucleus in the midline thalamus, was selectively activated by prolonged cold associated with elevated energy expenditure but not with acute cold exposure. In vivo calcium imaging showed that Xi activity correlates with food-seeking episodes under cold conditions. Using activity-dependent viral strategies, we found that optogenetic and chemogenetic stimulation of cold-activated Xi neurons selectively recapitulated food seeking under cold conditions whereas their inhibition suppressed it. Mechanistically, Xi encodes a context-dependent valence switch that promotes food-seeking behaviours under cold but not warm conditions. Furthermore, these behaviours are mediated by a Xi-to-nucleus accumbens projection. Our results establish Xi as a key region in the control of cold-induced feeding, which is an important mechanism in the maintenance of energy homeostasis in endothermic animals.

Publication Types

["Journal Article", "Research Support, Non-U.S. Gov't", "Research Support, N.I.H., Extramural"]

Keywords

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MeSH Terms

["Animals", "Mice", "Body Temperature", "Brain Mapping", "Calcium", "Feeding Behavior", "Cold Temperature", "Energy Metabolism", "Thalamus", "Optogenetics", "Neurons", "Nucleus Accumbens", "Homeostasis", "Thermogenesis", "Proto-Oncogene Proteins c-fos"]

Funding

R01 DK107717 NIDDK NIH HHS (United States)
R01 DK133948 NIDDK NIH HHS (United States)
R01 DK134609 NIDDK NIH HHS (United States)
K01 DK114165 NIDDK NIH HHS (United States)
R03 DK124731 NIDDK NIH HHS (United States)
DP2 DK128800 NIDDK NIH HHS (United States)
P30 DK135043 NIDDK NIH HHS (United States)
S10 OD028635 NIH HHS (United States)
RF1 MH132570 NIMH NIH HHS (United States)