TY - JOUR
T1 - The modulation of emotional and social behaviors by oxytocin signaling in limbic network
AU - Triana-Del Rio, Rodrigo
AU - Ranade, Sayali
AU - Guardado, Jahel
AU - LeDoux, Joseph
AU - Klann, Eric
AU - Shrestha, Prerana
N1 - Publisher Copyright:
Copyright © 2022 Triana-Del Rio, Ranade, Guardado, LeDoux, Klann and Shrestha.
PY - 2022/11/17
Y1 - 2022/11/17
N2 - Neuropeptides can exert volume modulation in neuronal networks, which account for a well-calibrated and fine-tuned regulation that depends on the sensory and behavioral contexts. For example, oxytocin (OT) and oxytocin receptor (OTR) trigger a signaling pattern encompassing intracellular cascades, synaptic plasticity, gene expression, and network regulation, that together function to increase the signal-to-noise ratio for sensory-dependent stress/threat and social responses. Activation of OTRs in emotional circuits within the limbic forebrain is necessary to acquire stress/threat responses. When emotional memories are retrieved, OTR-expressing cells act as gatekeepers of the threat response choice/discrimination. OT signaling has also been implicated in modulating social-exposure elicited responses in the neural circuits within the limbic forebrain. In this review, we describe the cellular and molecular mechanisms that underlie the neuromodulation by OT, and how OT signaling in specific neural circuits and cell populations mediate stress/threat and social behaviors. OT and downstream signaling cascades are heavily implicated in neuropsychiatric disorders characterized by emotional and social dysregulation. Thus, a mechanistic understanding of downstream cellular effects of OT in relevant cell types and neural circuits can help design effective intervention techniques for a variety of neuropsychiatric disorders.
AB - Neuropeptides can exert volume modulation in neuronal networks, which account for a well-calibrated and fine-tuned regulation that depends on the sensory and behavioral contexts. For example, oxytocin (OT) and oxytocin receptor (OTR) trigger a signaling pattern encompassing intracellular cascades, synaptic plasticity, gene expression, and network regulation, that together function to increase the signal-to-noise ratio for sensory-dependent stress/threat and social responses. Activation of OTRs in emotional circuits within the limbic forebrain is necessary to acquire stress/threat responses. When emotional memories are retrieved, OTR-expressing cells act as gatekeepers of the threat response choice/discrimination. OT signaling has also been implicated in modulating social-exposure elicited responses in the neural circuits within the limbic forebrain. In this review, we describe the cellular and molecular mechanisms that underlie the neuromodulation by OT, and how OT signaling in specific neural circuits and cell populations mediate stress/threat and social behaviors. OT and downstream signaling cascades are heavily implicated in neuropsychiatric disorders characterized by emotional and social dysregulation. Thus, a mechanistic understanding of downstream cellular effects of OT in relevant cell types and neural circuits can help design effective intervention techniques for a variety of neuropsychiatric disorders.
KW - emotional behavior
KW - intracellular cascades
KW - oxytocin
KW - oxytocin receptor (OTR)
KW - social behavior
KW - stress response
KW - threat response
UR - http://www.scopus.com/inward/record.url?scp=85143061812&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85143061812&partnerID=8YFLogxK
U2 - 10.3389/fnmol.2022.1002846
DO - 10.3389/fnmol.2022.1002846
M3 - Review article
AN - SCOPUS:85143061812
SN - 1662-5099
VL - 15
JO - Frontiers in Molecular Neuroscience
JF - Frontiers in Molecular Neuroscience
M1 - 1002846
ER -