A critical role for cortical amygdala circuitry in shaping social encounters.


Journal

Research square
Titre abrégé: Res Sq
Pays: United States
ID NLM: 101768035

Informations de publication

Date de publication:
06 Jul 2023
Historique:
pubmed: 18 7 2023
medline: 18 7 2023
entrez: 18 7 2023
Statut: epublish

Résumé

Aggression is an evolutionarily conserved behavior that controls social hierarchies and protects valuable resources like mates, food, and territory. In mice, aggressive behaviour can be broken down into an appetitive phase, which involves approach and investigation, and a consummatory phase, which involves biting, kicking, and wrestling. By performing an unsupervised weighted correlation network analysis on whole-brain c-Fos expression, we identified a cluster of brain regions including hypothalamic and amygdalar sub-regions and olfactory cortical regions highly co-activated in male, but not female aggressors (AGG). The posterolateral cortical amygdala (COApl), an extended olfactory structure, was found to be a hub region based on the number and strength of correlations with other regions in the cluster. Our data further show that estrogen receptor 1 (ESR1)-expressing cells in the COApl exhibit increased activity during attack behaviour, and during bouts of investigation which precede an attack, in male mice only. Chemogenetic or optogenetic inhibition of COApl ESR1 cells in AGG males reduces aggression and increases pro-social investigation without affecting social reward/reinforcement behavior. We further confirmed that COApl ESR1 projections to the ventrolateral portion of the ventromedial hypothalamus and central amygdala are necessary for these behaviours. Collectively, these data suggest that in aggressive males, COApl ESR1 cells respond specifically to social stimuli, thereby enhancing their salience and promoting attack behaviour.

Identifiants

pubmed: 37461537
doi: 10.21203/rs.3.rs-3015820/v1
pmc: PMC10350173
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH104559
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH120514
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH127820
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH114882
Pays : United States
Organisme : NIDA NIH HHS
ID : K99 DA058213
Pays : United States

Auteurs

Russo Scott (R)

Icahn School of Medicine at Mount Sinai.

Antonio Aubry (A)

Icahn School of Medicine at Mount Sinai.

Fisher-Foye Rachel (FF)

Icahn School of Medicine at Mt. Sinai.

Flurin Cathomas (F)

Icahn School of Medicine at Mount Sinai.

C Burnett (C)

Icahn School of Medicine at Mount Sinai.

Yewon Yang (Y)

Icahn School of Medicine at Mt. Sinai.

Chongzhen Yuan (C)

Icahn School of Medicine at Mt. Sinai.

Alexa Lablanca (A)

Icahn School of Medicine at Mt. Sinai.

Kenny Chan (K)

Icahn School of Medicine at Mount Sinai.

Hsiao-Yun Lin (HY)

Icahn School of Medicine at Mount Sinai.

Long Li (L)

Icahn School of Medicine at Mount Sinai.

Classifications MeSH