Cited by 381Neuroendocrine regulation and behaviorMemory and Neural MechanismsNeuropeptides and Animal Physiology

Oxytocin Selectively Gates Fear Responses Through Distinct Outputs from the Central Amygdala

Viviani, Daniele, Charlet, Alexandre, van den Burg, Erwin, Robinet, Camille, Hurni, Nicolas, Abatis, Marios, Magara, Fulvio, Stoop, Ron·2011·Science

Abstract

Specific neuronal populations in the amygdala control different behavioral and physiological components of the fear response.

Integrity signals

Registry

Crossref · 10.1126/science.1201043

Cites

28 of 28 references verified0 citation errors · 0 not checkable

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  • Within the rodent central amygdala, oxytocin receptor density differs across subdivisions.

    “OT receptor density varies by subdivision within the central nucleus of the rodent amygdala (CeA)4,6”

    From Oxytocin increases anxiety to unpredictable threat (2013) · cites this paper as [4]

  • In animals, oxytocin can lessen anxiety-like behavior through its modulatory action on the amygdala.

    “Indeed, OT can reduce anxiety-like behavior in animals, via its neuromodulatory influence on the amygdala, a core hub mediating fear and anxiety.4”

    From Oxytocin increases anxiety to unpredictable threat (2013) · cites this paper as [4]

  • The implication of CeA OXT signaling in processing threat responses and social fear suggests a specific role in detection of fear-mediated responses.

    “The implication of CeA OXT signaling in processing threat responses [22,94,104] and social fear [105] would suggest a specific role in the detection of fear-mediated responses.”
  • Distinct neuronal populations in sub-regions of the amygdala control specific behavioral responses to fear.

    “Distinct neuronal populations in sub-regions of the amygdala have indeed been shown to control specific behavioral responses to fear [104, 108]”
  • Previous studies have shown that oxytocin receptors in the amygdala potentiate GABAergic inhibition.

    “Previous studies have shown that OXT receptors in the amygdala potentiate GABAergic inhibition (ie, Huber et al, 2005;Viviani et al, 2011).”

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Authors
Viviani, D., Charlet, A., van den Burg, E., Robinet, C., Hurni, N., Abatis, M., Magara, F., & Stoop, R.
Affiliations
  • Centre Hospitalier Universitaire Vaudois (CH)
  • Centre for Psychiatric Neuroscience, Department of Psychiatry, Lausanne University Hospital Center, University of Lausanne, CH-1015 Lausanne, Switzerland.
Corresponding author
  • Robinet, Camille
  • Stoop, Ron
Venue
Science
Published
2011-07
Volume
333
Issue
6038
Pages
104-107
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2091857612
Cited by
381
References
28
Citations by year
2026: 13 · 2025: 9 · 2024: 22 · 2023: 13 · 2022: 19 · 2021: 29 · 2020: 32 · 2019: 18 · 2018: 33 · 2017: 33 · 2016: 28 · 2015: 34 · 2014: 39 · 2013: 27 · 2012: 26
FWCI
41.72
Type
journal article
Language
en
Open access
closed
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
  • IRIS (submittedVersion)
  • SERVAL (Université de Lausanne) (submittedVersion)
Topics
  • Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Keywords
oxytocin, central amygdala, fear response, freezing behavior, cardiovascular response, hypothalamic projections, neuronal subpopulations, fear conditioning, neural circuits
MeSH terms
Amygdala, Animals, Bombesin, Brain Stem, Conditioning, Psychological, Fear, Female, Heart Rate, Hypothalamus, Male, Muscimol, Neural Inhibition, Neural Pathways, Neurons, Oxytocin, Periaqueductal Gray, Rats, Sprague-Dawley, Patch-Clamp Techniques, Rats, GABA-A Receptor Agonists

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