Literature DB >> 33441435

Hypothalamic-Extended Amygdala Circuit Regulates Temporal Discounting.

Haofang E Li1, Mark A Rossi1, Glenn D R Watson1, H Gregory Moore1, Min Tong Cai1, Namsoo Kim1, Katrina A Vokt1, Dongye Lu1, Ryan A Bartholomew1, Ryan N Hughes1, Henry H Yin2.   

Abstract

Choice behavior is characterized by temporal discounting, i.e., preference for immediate rewards given a choice between immediate and delayed rewards. Agouti-related peptide (AgRP)-expressing neurons located in the arcuate nucleus of the hypothalamus (ARC) regulate food intake and energy homeostasis, yet whether AgRP neurons influence choice behavior and temporal discounting is unknown. Here, we demonstrate that motivational state potently modulates temporal discounting. Hungry mice (both male and female) strongly preferred immediate food rewards, yet sated mice were largely indifferent to reward delay. More importantly, selective optogenetic activation of AgRP-expressing neurons or their axon terminals within the posterior bed nucleus of stria terminalis (BNST) produced temporal discounting in sated mice. Furthermore, activation of neuropeptide Y (NPY) type 1 receptors (Y1Rs) within the BNST is sufficient to produce temporal discounting. These results demonstrate a profound influence of hypothalamic signaling on temporal discounting for food rewards and reveal a novel circuit that determine choice behavior.SIGNIFICANCE STATEMENT Temporal discounting is a universal phenomenon found in many species, yet the underlying neurocircuit mechanisms are still poorly understood. Our results revealed a novel neural pathway from agouti-related peptide (AgRP) neurons in the hypothalamus to the bed nucleus of stria terminalis (BNST) that regulates temporal discounting in decision-making.
Copyright © 2021 the authors.

Entities:  

Keywords:  AgRP; bed nucleus of stria terminalis; decision making; delay discounting; neuropeptide Y; reward

Year:  2021        PMID: 33441435      PMCID: PMC7939087          DOI: 10.1523/JNEUROSCI.1836-20.2020

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  52 in total

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