作者
Jérôme Wahis,Angel Baudon,Ferdinand Althammer,Damien Kerspern,Stéphanie Goyon,Daisuke Hagiwara,Arthur Lefèvre,Lara Barteczko,Benjamin Boury‐Jamot,Benjamin Bellanger,Marios Abatis,Miriam Da Silva Gouveia,Diego Benusiglio,Marina Eliava,Andrei Rozov,Ivan Weinsanto,H. Sophie Knobloch‐Bollmann,Matthew K. Kirchner,Ranjan K. Roy,Hong Wang,Marie Pertin,Perrine Inquimbert,Claudia Pitzer,Jan Siemens,Yannick Goumon,Benjamin Boutrel,Christophe M. Lamy,Isabelle Décosterd,Jean‐Yves Chatton,Nathalie Rouach,W. Scott Young,Javier E. Stern,Pierrick Poisbeau,Ron Stoop,Pascal Darbon,Valery Grinevich,Alexandre Charlet
摘要
Oxytocin (OT) orchestrates social and emotional behaviors through modulation of neural circuits. In the central amygdala, the release of OT modulates inhibitory circuits and, thereby, suppresses fear responses and decreases anxiety levels. Using astrocyte-specific gain and loss of function and pharmacological approaches, we demonstrate that a morphologically distinct subpopulation of astrocytes expresses OT receptors and mediates anxiolytic and positive reinforcement effects of OT in the central amygdala of mice and rats. The involvement of astrocytes in OT signaling challenges the long-held dogma that OT acts exclusively on neurons and highlights astrocytes as essential components for modulation of emotional states under normal and chronic pain conditions. This study shows that a subpopulation of astrocytes in the central amygdala (CeA) expresses the oxytocin receptor (OTR) and that OTR activation in astrocytes underlies the anxiolytic and positive reinforcement effects of oxytocin in the CeA.