TY - JOUR
T1 - Integration of hunger and hormonal state gates infant-directed aggression
AU - Cao, Mingran
AU - Ammari, Rachida
AU - Chen, Maxwell X.
AU - Wai, Patty
AU - Jamieson, Bradley B.
AU - Liang, Swang
AU - Husain, Basma F.A.
AU - Sahni, Aashna
AU - Legrave, Nathalie
AU - Salgarella, Irene
AU - MacRae, James
AU - Strom, Molly
AU - Kohl, Johannes
N1 - Funding:
This study received support from the Francis Crick Institute (core funding FC001153). The Francis Crick Institute receives its funding from Cancer Research UK, the UK Medical Research Council and the Wellcome Trust (to J.K.). This study was also supported by a European Research Council starting grant (ERC-2019-STG847873 to J.K.), a NARSAD Young Investigator Award (BB/V016946/1 to J.K.) and a Boehringer Ingelheim PhD fellowship (to M.C.)
Publisher Copyright:
© The Author(s) 2025.
PY - 2025/10/22
Y1 - 2025/10/22
N2 - Social behaviour is substantially shaped by internal physiological states. Although progress has been made in understanding how individual states such as hunger, stress or arousal modulate behaviour1, 2, 3, 4, 5, 6, 7, 8–9, animals experience multiple states at any given time10. The neural mechanisms that integrate such orthogonal states—and how this integration affects behaviour—remain poorly understood. Here we report how hunger and oestrous state converge on neurons in the medial preoptic area (MPOA) to shape infant-directed behaviour. We find that hunger promotes pup-directed aggression in normally non-aggressive virgin female mice. This behavioural switch occurs through the inhibition of MPOA neurons, driven by the release of neuropeptide Y from Agouti-related peptide-expressing neurons in the arcuate nucleus (ArcAgRP neurons). The propensity for hunger-induced aggression is set by reproductive state, with MPOA neurons detecting changes in the progesterone to oestradiol ratio across the oestrous cycle. Hunger and oestrous state converge on hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, which sets the baseline activity and excitability of MPOA neurons. Using microendoscopy imaging, we confirm these findings in vivo, revealing that MPOA neurons encode a state for pup-directed aggression. This work provides a mechanistic understanding of how multiple physiological states are integrated to flexibly control social behaviour.
AB - Social behaviour is substantially shaped by internal physiological states. Although progress has been made in understanding how individual states such as hunger, stress or arousal modulate behaviour1, 2, 3, 4, 5, 6, 7, 8–9, animals experience multiple states at any given time10. The neural mechanisms that integrate such orthogonal states—and how this integration affects behaviour—remain poorly understood. Here we report how hunger and oestrous state converge on neurons in the medial preoptic area (MPOA) to shape infant-directed behaviour. We find that hunger promotes pup-directed aggression in normally non-aggressive virgin female mice. This behavioural switch occurs through the inhibition of MPOA neurons, driven by the release of neuropeptide Y from Agouti-related peptide-expressing neurons in the arcuate nucleus (ArcAgRP neurons). The propensity for hunger-induced aggression is set by reproductive state, with MPOA neurons detecting changes in the progesterone to oestradiol ratio across the oestrous cycle. Hunger and oestrous state converge on hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, which sets the baseline activity and excitability of MPOA neurons. Using microendoscopy imaging, we confirm these findings in vivo, revealing that MPOA neurons encode a state for pup-directed aggression. This work provides a mechanistic understanding of how multiple physiological states are integrated to flexibly control social behaviour.
UR - https://www.scopus.com/pages/publications/105019618537
UR - https://pubmed.ncbi.nlm.nih.gov/41125886/
U2 - 10.1038/s41586-025-09651-2
DO - 10.1038/s41586-025-09651-2
M3 - Article
C2 - 41125886
AN - SCOPUS:105019618537
SN - 0028-0836
JO - Nature
JF - Nature
ER -