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Species-typical group size differentially influences social reward neural circuitry during nonreproductive social interactions

  • Jose A. Gonzalez Abreu
  • , Ashley E. Rosenberg
  • , Brandon A. Fricker
  • , Kelly J. Wallace
  • , Ashley W. Seifert
  • , Aubrey M. Kelly

Producción científica: Articlerevisión exhaustiva

17 Citas (Scopus)

Resumen

We investigated whether nonreproductive social interactions may be rewarding for colonial but not non-colonial species. We found that the colonial spiny mouse (Acomys cahirinus) is significantly more gregarious, more prosocial, and less aggressive than its non-colonial relative, the Mongolian gerbil (Meriones unguiculatus). In an immediate-early gene study, we examined oxytocin (OT) and tyrosine hydroxylase (TH) neural responses to interactions with a novel, same-sex conspecific or a novel object. The paraventricular nucleus of the hypothalamus (PVN) OT cell group was more responsive to interactions with a conspecific compared to a novel object in both species. However, the ventral tegmental area (VTA) TH cell group showed differential responses only in spiny mice. Further, PVN OT and VTA TH neural responses positively correlated in spiny mice, suggesting functional connectivity. These results suggest that colonial species may have evolved neural mechanisms associated with reward in novel, nonreproductive social contexts to promote large group-living.

Idioma originalEnglish
Número de artículo104230
PublicacióniScience
Volumen25
N.º5
DOI
EstadoPublished - may 20 2022

Nota bibliográfica

Publisher Copyright:
© 2022 The Author(s)

Financiación

We would like to acknowledge funding from the Klingenstein-Simons Foundation (Fellowship Award in Neuroscience to AMK ), the National Institute of Arthritis and Musculoskeletal and Skin Diseases ( R01AR070313 to AWS ), and the National Science Foundation ( IOS-1353713 to AWS ).

FinanciadoresNúmero del financiador
Klingenstein-Simons Foundation
National Science Foundation Arctic Social Science Program1353713, IOS-1353713
National Institute of Arthritis and Musculoskeletal and Skin DiseasesR01AR070313

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