# Neuropeptide Y neurons in the basolateral amygdala project to the nucleus accumbens and stimulate high-fat intake

## TL;DR

This study shows that neurons in the amygdala that release NPY connect to the nucleus accumbens and influence high-fat food consumption in mice.

## Contribution

The paper identifies a specific neural pathway involving NPY neurons from the BLA to the NAc that regulates high-fat diet intake.

## Key findings

- Optogenetic inactivation of BLA NPY neurons reduced high-fat diet intake in mice.
- Activation of these neurons increased high-fat diet consumption.
- Blocking Y1R in the NAc decreased high-fat diet intake, while activating Y1R increased it.

## Abstract

Neuropeptide Y (NPY) is a 36-amino acid neuropeptide that is widely expressed in the central nervous system, including in the nucleus accumbens (NAc), hypothalamus, and amygdala. The NAc involved in several behaviors, including reward, motivation processes, and feeding behavior. Here, we demonstrate in male mice that NPY input from the basolateral amygdala (BLA) to the NAc is involved in the preferential consumption of a high-fat diet (HFD). First, we demonstrated the NPY input to the NAc from the BLA by injecting adeno-associated virus (AAV)(retro)-FLEX-mCherry into the NAc of NPY-Cre mice. We also confirmed that BLA NPY neurons project exclusively to the NAc by injecting AAV(dj)-hSyn-FLEx -mGFP-2A-Synaptophysin-mRuby into the BLA. Usually, a HFD drives enhanced food intake than a standard chow diet after repetitive exposure. The optogenetic inactivation of BLA NPY neurons projecting to the NAc caused a significant decrease in HFD intake for a 1-h period, while optogenetic activation of these neurons induced the opposite effect. Furthermore, bilateral injection of an NPY receptor type 1 (Y1R) antagonist into the NAc significantly decreased HFD intake for 1-h period compared with vehicle injection, while, conversely, injection of a Y1R agonist enhanced HFD intake. These results suggest that BLA NPY neurons projecting to the NAc mediate preferential HFD intake via NAc-localized Y1R.