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A brain-derived insulin signal encodes protein satiety for nutrient-specific feeding inhibition

  • Xiaoyu Li
  • , Yang Yang
  • , Xiaobing Bai
  • , Xiaotong Wang
  • , Houqi Tan
  • , Yanbo Chen
  • , Yan Zhu
  • , Qili Liu
  • , Mark N. Wu
  • , Yan Li

Research output: Contribution to journalArticlepeer-review

Abstract

The suppressive effect of insulin on food intake has been documented for decades. However, whether insulin signals can encode a certain type of nutrients to regulate nutrient-specific feeding behavior remains elusive. Here, we show that in female Drosophila, a pair of dopaminergic neurons, tritocerebrum 1-dopaminergic neurons (T1-DANs), are directly activated by a protein-intake-induced insulin signal from insulin-producing cells (IPCs). Intriguingly, opto-activating IPCs elicits feeding inhibition for both protein and sugar, while silencing T1-DANs blocks this inhibition only for protein food. Elevating insulin signaling in T1-DANs or opto-activating these neurons is sufficient to mimic protein satiety. Furthermore, this signal is conveyed to local neurons of the protocerebral bridge (PB-LNs) and specifically suppresses protein intake. Therefore, our findings reveal that a brain-derived insulin signal encodes protein satiety and suppresses feeding behavior in a nutrient-specific manner, shedding light on the functional specificity of brain insulin signals in regulating behaviors.

Original languageEnglish (US)
Article number114282
JournalCell Reports
Volume43
Issue number6
DOIs
StatePublished - Jun 25 2024

Keywords

  • CP: Neuroscience
  • brain insulin signals
  • dopaminergic neurons
  • feeding inhibition
  • protein satiety

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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