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Life sciences · Journal article
Nature Communications · September 16, 2026
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Obesity and anxiety disorders are frequently comorbid, yet the neural circuit mechanisms linking metabolic and affective states remain incompletely understood. Here, in male mice exposed to long-term high-fat diet, we identify a hypothalamic circuit comprising arcuate nucleus agouti-related protein neurons and paraventricular nucleus corticotropin-releasing hormone neurons that regulates anxiety-like behavior under metabolic stress, with downstream recruitment of lateral hypothalamic area glutamatergic neurons to modulate feeding in a state-dependent manner. In vivo fiber photometry and ex vivo electrophysiology show that high-fat diet enhances activity and feeding-locked recruitment of this circuit, associated with increased anxiety-like behavior and feeding. Circuit-specific inhibition attenuates both phenotypes, whereas corticotropin-releasing hormone receptor 2 signaling in the lateral hypothalamic area selectively mediates high-fat diet-associated hyperphagia without affecting anxiety-like behavior. In this work, we show a disease-state-dependent hypothalamic circuit differentially recruited under chronic high-fat diet to coordinate anxiety-related behavior and feeding output, providing a framework for metabolic-affective interactions. Obesity and anxiety often co-occur, but their neural link is unclear. Here, authors show that an Arc-PVN-LHA hypothalamic circuit coordinates HFD-associated anxiety-like behavior and feeding in a state-dependent manner.