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A Hypothalamic Circuit Underlying the Dynamic Control of Social Homeostasis

Social grouping increases survival in many species, including humans(1,2). By contrast, social isolation generates an aversive state (loneliness) that motivates social seeking and heightens social interaction upon reunion(3–5). The observed rebound in social interaction triggered by isolation sugges...

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Detalles Bibliográficos
Autores principales: Liu, Ding, Rahman, Mostafizur, Johnson, Autumn, Tsutsui-Kimura, Iku, Pena, Nicolai, Talay, Mustafa, Logeman, Brandon L., Finkbeiner, Samantha, Choi, Seungwon, Capo-Battaglia, Athena, Abdus-Saboor, Ishmail, Ginty, David D., Uchida, Naoshige, Watabe-Uchida, Mitsuko, Dulac, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245688/
https://www.ncbi.nlm.nih.gov/pubmed/37293031
http://dx.doi.org/10.1101/2023.05.19.540391
Descripción
Sumario:Social grouping increases survival in many species, including humans(1,2). By contrast, social isolation generates an aversive state (loneliness) that motivates social seeking and heightens social interaction upon reunion(3–5). The observed rebound in social interaction triggered by isolation suggests a homeostatic process underlying the control of social drive, similar to that observed for physiological needs such as hunger, thirst or sleep(3,6). In this study, we assessed social responses in multiple mouse strains and identified the FVB/NJ line as exquisitely sensitive to social isolation. Using FVB/NJ mice, we uncovered two previously uncharacterized neuronal populations in the hypothalamic preoptic nucleus that are activated during social isolation and social rebound and that orchestrate the behavior display of social need and social satiety, respectively. We identified direct connectivity between these two populations of opposite function and with brain areas associated with social behavior, emotional state, reward, and physiological needs, and showed that animals require touch to assess the presence of others and fulfill their social need, thus revealing a brain-wide neural system underlying social homeostasis. These findings offer mechanistic insight into the nature and function of circuits controlling instinctive social need and for the understanding of healthy and diseased brain states associated with social context.