Enhanced social interactions in rats following chronic, centrally infused oxytocin
Abstract
Most studies investigating the behavioral effects of centrally administered oxytocin (OT) have been confined to single acute injections followed by brief behavioral observations lasting up to 90 min. The present study examines the behavioral effects of chronic, centrally administered OT in male rats observed continuously for prolonged periods of time. Either artificial cerebrospinal fluid or OT was centrally infused (via osmotic minipump) to gonadally intact male rats. Behavioral observations were made on males paired with either ovariectomized or estrous females during a 6-h time period. Most striking was the observation that durations of physical contact were doubled in pairs containing OT-infused males, even in the absence of sexual interactions. Also, OT-infused males showed significantly higher levels of anogenital sniffing of females and autogrooming; however, sexual interactions were unaffected by chronic OT. Chronic OT had no effect on body temperature, analgesia, or exploratory behavior in an open field. These findings suggest that chronic OT in male rats has behavioral effects that may significantly enhance adult social (nonsexual) interactions, possibly through alterations in olfactory and somatosensory information processing.
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Centrally administered oxytocin facilitates contact-seeking, attachment bond formation, and social memory in rodents.
“Centrally administered OT facilitates contact-seeking, attachment bond formation, and social memory in rodents (Ferguson et al., 2000; Williams et al., 1992; Witt et al., 1992).”
From Effects of intranasal oxytocin on social anxiety in males with fragile X syndrome (2012) · cites this paper as Witt et al., 1992
Intranasal oxytocin administration in fragile X syndrome may work mechanistically by dampening amygdala reactivity toward socially threatening and anxiety-provoking stimuli, decreasing HPA axis activation, and increasing social motivation.
“Intranasal OT administration in FXS may work mechanistically by dampening amygdala reactivity toward socially threatening and anxiety-provoking stimuli (Kirsch et al., 2005; Petrovic et al., 2008), decreasing HPA axis activation, and increasing social motivation (Witt et al., 1992).”
From Effects of intranasal oxytocin on social anxiety in males with fragile X syndrome (2012) · cites this paper as Witt et al., 1992
Seminal studies in male-male and male-female rodent pairs have contributed to the notion of OT as a facilitator of affiliative behaviors.
“While seminal studies in male-male and male-female rodent pairs have contributed to the notion of OT as a facilitator of affiliative behaviors (Lukas et al., 2011, Williams et al., 1994, Witt et al., 1992), recent findings also provide evidence of antisocial effects of OT (van Anders et al., 2013, Bartz et al., 2011, Beery, 2015).”
From Wireless Optogenetic Stimulation of Oxytocin Neurons in a Semi-natural Setup Dynamically Elevates Both Pro-social and Agonistic Behaviors (2020) · cites this paper as Witt et al., 1992
Intranasal oxytocin enhances prosocial and affiliative behaviors in rodents and non-human primates.
“Intranasal oxytocin is also known to enhance prosocial and affiliative behaviors in rodents (Ferguson et al., 2001; Witt et al., 1992) and non-human primates (Chang and Platt, 2013).”
From Effects of adverse childhood experiences on the association between intranasal oxytocin and social stress reactivity among individuals with cocaine dependence (2015) · cites this paper as Witt et al., 1992
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- Authors
- Witt, D. M., Winslow, J. T., & Insel, T. R.
- Affiliations
- National Institute of Mental Health (US)
- Corresponding author
- Witt, Diane M.
- ORCID
- Insel, Thomas R.
- Venue
- Pharmacology Biochemistry and Behavior
- Publisher
- Elsevier BV
- Published
- 1992-11
- Volume
- 43
- Issue
- 3
- Pages
- 855-861
- ISSN
- 0091-3057 (ISSN-L)
- OpenAlex
- W2022479132
- Cited by
- 244
- References
- 29
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 1 · 2023: 1 · 2022: 5 · 2021: 11 · 2020: 4 · 2019: 9 · 2018: 8 · 2017: 10 · 2016: 16 · 2015: 10 · 2014: 16 · 2013: 18 · 2012: 8
- FWCI
- 6.18
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Pharmacology Biochemistry and Behavior (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- oxytocin, social interaction, physical contact, anogenital sniffing, autogrooming, sexual behavior, olfactory processing, somatosensory processing, ovariectomized females, estrous cycle, body temperature, analgesia, exploratory behavior
- MeSH terms
- Analgesia, Animals, Arousal, Body Temperature Regulation, Estradiol, Exploratory Behavior, Female, Grooming, Injections, Intraventricular, Interpersonal Relations, Male, Motor Activity, Ovariectomy, Oxytocin, Sexual Behavior, Animal, Stimulation, Chemical, Rats, Sprague-Dawley, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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