Abstract

The gustatory system plays a critical role in sensing appetitive and aversive taste stimuli for evaluating food quality. Although taste preference is known to change depending on internal states such as hunger, a mechanistic insight remains unclear. Here, we examine the neuronal mechanisms regulating hunger-induced taste modification. Starved mice exhibit an increased preference for sweetness and tolerance for aversive taste. This hunger-induced taste modification is recapitulated by selective activation of orexigenic Agouti-related peptide (AgRP)-expressing neurons in the hypothalamus projecting to the lateral hypothalamus, but not to other regions. Glutamatergic, but not GABAergic, neurons in the lateral hypothalamus function as downstream neurons of AgRP neurons. Importantly, these neurons play a key role in modulating preferences for both appetitive and aversive tastes by using distinct pathways projecting to the lateral septum or the lateral habenula, respectively. Our results suggest that these hypothalamic circuits would be important for optimizing feeding behavior under fasting.

Highlights

  • The gustatory system plays a critical role in sensing appetitive and aversive taste stimuli for evaluating food quality

  • We demonstrate that physiological hunger affects preferences to both appetitive and aversive tastes and these effects are recapitulated by artificial activation of the lateral hypothalamus (LHA)-projecting Agouti-related peptide (AgRP) neurons

  • We found a dense innervation in the paraventricular nucleus of the hypothalamus (PVH), the LHA, and the central nucleus of the amygdala (CEA) as reported previously (Supplementary Fig. 4B)[14]

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Summary

Introduction

The gustatory system plays a critical role in sensing appetitive and aversive taste stimuli for evaluating food quality. The brief access taste test demonstrated that chemogenetic inhibition of AgRP neurons reverses either appetitive or aversive taste preference under physiological hunger conditions (Fig. 1j, k). To determine which projection area of AgRP neurons regulates taste preferences, we first visualized the axon terminals of AgRP neurons by injecting the anterograde tracer AAV (AAV-hEF1a-DIO-synaptophysin-mCherry) into AgRP-ires-Cre mice (Supplementary Fig. 4A).

Results
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