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A neural pathway underlying hunger modulation of sexual receptivity in Drosophila females.

Abstract
Accepting or rejecting a mate is one of the most crucial decisions a female will make, especially when faced with food shortage. Previous studies have identified the core neural circuity from sensing male courtship or mating status to decision-making for sexual receptivity in Drosophila females, but how hunger and satiety states modulate female receptivity is poorly understood. Here, we identify the neural circuit and its neuromodulation underlying the hunger modulation of female receptivity. We find that adipokinetic hormone receptor (AkhR)-expressing neurons inhibit sexual receptivity in a starvation-dependent manner. AkhR neurons are octopaminergic and act on a subset of Octβ1R-expressing LH421 neurons. Knocking down Octβ1R expression in LH421 neurons eliminates starvation-induced suppression of female receptivity. We further find that LH421 neurons inhibit the sex-promoting pC1 neurons via GABA-resistant to dieldrin (Rdl) signaling. pC1 neurons also integrate courtship stimulation and mating status and thus serve as a common integrator of multiple internal and external cues for decision-making.
AuthorsMengshi Sun, Mingze Ma, Bowen Deng, Na Li, Qionglin Peng, Yufeng Pan
JournalCell reports (Cell Rep) Vol. 42 Issue 10 Pg. 113243 (10 31 2023) ISSN: 2211-1247 [Electronic] United States
PMID37819758 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.
Chemical References
  • Drosophila Proteins
Topics
  • Animals
  • Female
  • Male
  • Drosophila (metabolism)
  • Drosophila melanogaster (metabolism)
  • Drosophila Proteins (metabolism)
  • Hunger
  • Sexual Behavior, Animal (physiology)
  • Neural Pathways (metabolism)
  • Courtship

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