2025/04/22 by Katy Celina Sandoval, Joshua Rychlik, Katrina Y. Choe · 1 voice
Psychology · Neuroscience · #Neuroendocrine regulation and behavior #Stress Responses and Cortisol #Neuroscience of respiration and sleep
paper · pdf · doi:10.1523/eneuro.0196-24.2025
openalex publication_date 2025/04/22 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/18
Activation of hypothalamic paraventricular oxytocin (OXT PVN ) neurons by social or stress stimuli triggers OXT release to promote social investigation and buffer adverse effects of stress, respectively. Astrocytes, a type of glial cells, can bidirectionally interact with hypothalamic neurons to participate in local activity regulation within the paraventricular nucleus (PVN). It remains unknown whether contextual factors related to stimuli, as well as biological factors such as sex, influence OXT PVN neuronal or astrocyte activity and/or their interactions. To address this question, we performed dual-color fiber photometry in freely behaving male and female mice to simultaneously record Ca 2+ dynamics in OXT PVN neurons and astrocytes during acute social (i.e., interactions with familiar vs. unfamiliar conspecifics) and stress (i.e., looming shadow) stimuli. During social stimuli, we observed the most pronounced Ca 2+ changes in OXT PVN neurons in females, revealing sex and familiarity context specificity. No astrocyte Ca 2+ changes were detected in either sex regardless of conspecific familiarity. In contrast, looming shadow stress increased Ca 2+ in both OXT PVN neurons and astrocytes in both sexes during an active escape (“run”) strategy. Ca 2+ level changes in OXT PVN neurons and astrocytes were significantly correlated during social investigations in both sexes regardless of conspecific familiarity. During looming shadow, this functional coupling was only observed in females during active escape. Together, our results suggest that sex, context, and behavioral strategy serve as major factors that shape the activity of OXT PVN neurons and astrocytes, as well as their functional coupling, to potentially aid the adaptive response to social or stress stimuli.