| Literature DB >> 32719563 |
Yan Tang1,2, Diego Benusiglio1, Arthur Lefevre1,3, Louis Hilfiger3, Ferdinand Althammer1,4, Anna Bludau5, Daisuke Hagiwara1, Angel Baudon3, Pascal Darbon3, Jonas Schimmer1, Matthew K Kirchner4, Ranjan K Roy4, Shiyi Wang1, Marina Eliava1, Shlomo Wagner6, Martina Oberhuber7, Karl K Conzelmann7, Martin Schwarz8, Javier E Stern4, Gareth Leng9, Inga D Neumann5, Alexandre Charlet10, Valery Grinevich11,12.
Abstract
Oxytocin (OT) is a great facilitator of social life but, although its effects on socially relevant brain regions have been extensively studied, OT neuron activity during actual social interactions remains unexplored. Most OT neurons are magnocellular neurons, which simultaneously project to the pituitary and forebrain regions involved in social behaviors. In the present study, we show that a much smaller population of OT neurons, parvocellular neurons that do not project to the pituitary but synapse onto magnocellular neurons, is preferentially activated by somatosensory stimuli. This activation is transmitted to the larger population of magnocellular neurons, which consequently show coordinated increases in their activity during social interactions between virgin female rats. Selectively activating these parvocellular neurons promotes social motivation, whereas inhibiting them reduces social interactions. Thus, parvocellular OT neurons receive particular inputs to control social behavior by coordinating the responses of the much larger population of magnocellular OT neurons.Entities:
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Year: 2020 PMID: 32719563 DOI: 10.1038/s41593-020-0674-y
Source DB: PubMed Journal: Nat Neurosci ISSN: 1097-6256 Impact factor: 24.884