Sex-Specific Effects of Stress on Oxytocin Neurons Correspond With Responses to Intranasal Oxytocin

Michael Q. Steinman, Natalia Duque-Wilckens, Gian D. Greenberg, Rebecca Hao, Katharine L. Campi, Sarah A. Laredo, Abigail Laman-Maharg, Claire E. Manning, Ian E. Doig, Eduardo M. Lopez, Keenan Walch, Karen L. Bales, Brian C. Trainor

Research output: Contribution to journalArticle

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Abstract

Background Oxytocin (OT) is considered to be a stress-buffering hormone, dampening the physiologic effects of stress. However, OT can also be anxiogenic. We examined acute and long-lasting effects of social defeat on OT neurons in male and female California mice. Methods We used immunohistochemistry for OT and c-fos cells to examine OT neuron activity immediately after defeat (n = 6–9) and 2 weeks (n = 6–9) and 10 weeks (n = 4–5) later. We quantified Oxt messenger RNA with quantitative polymerase chain reaction (n = 5–9). Intranasal OT was administered to naïve and stressed mice tested in social interaction and resident-intruder tests (n = 8–14). Results Acute exposure to a third episode of defeat increased OT/c-fos colocalizations in the paraventricular nucleus of both sexes. In the medioventral bed nucleus of the stria terminalis, defeat increased Oxt messenger RNA, total OT neurons, and OT/c-fos colocalizations in female mice but not male mice. Intranasal OT failed to reverse stress-induced social withdrawal in female mice and reduced social interaction behavior in female mice naïve to defeat. In contrast, intranasal OT increased social interaction in stressed male mice and reduced freezing in the resident-intruder test. Conclusions Social defeat induces long-lasting increases in OT production and OT/c-fos cells in the medioventral bed nucleus of the stria terminalis of female mice but not male mice. Intranasal OT largely reversed the effects of stress on behavior in male mice, but effects were mixed in female mice. These results suggest that changes in OT-sensitive networks contribute to sex differences in behavioral responses to stress.

Original languageEnglish (US)
Pages (from-to)406-414
Number of pages9
JournalBiological Psychiatry
Volume80
Issue number5
DOIs
StatePublished - Sep 1 2016

Fingerprint

Oxytocin
Neurons
Interpersonal Relations
Septal Nuclei
Messenger RNA
Paraventricular Hypothalamic Nucleus
Sex Characteristics
Freezing

Keywords

  • Anxiety
  • Bed nucleus of the stria terminalis
  • Mood disorders
  • Oxytocin
  • Paraventricular nucleus
  • Peromyscus
  • Posttraumatic stress disorder
  • Sex differences
  • Social behavior

ASJC Scopus subject areas

  • Biological Psychiatry

Cite this

Steinman, M. Q., Duque-Wilckens, N., Greenberg, G. D., Hao, R., Campi, K. L., Laredo, S. A., ... Trainor, B. C. (2016). Sex-Specific Effects of Stress on Oxytocin Neurons Correspond With Responses to Intranasal Oxytocin. Biological Psychiatry, 80(5), 406-414. https://doi.org/10.1016/j.biopsych.2015.10.007

Sex-Specific Effects of Stress on Oxytocin Neurons Correspond With Responses to Intranasal Oxytocin. / Steinman, Michael Q.; Duque-Wilckens, Natalia; Greenberg, Gian D.; Hao, Rebecca; Campi, Katharine L.; Laredo, Sarah A.; Laman-Maharg, Abigail; Manning, Claire E.; Doig, Ian E.; Lopez, Eduardo M.; Walch, Keenan; Bales, Karen L.; Trainor, Brian C.

In: Biological Psychiatry, Vol. 80, No. 5, 01.09.2016, p. 406-414.

Research output: Contribution to journalArticle

Steinman, MQ, Duque-Wilckens, N, Greenberg, GD, Hao, R, Campi, KL, Laredo, SA, Laman-Maharg, A, Manning, CE, Doig, IE, Lopez, EM, Walch, K, Bales, KL & Trainor, BC 2016, 'Sex-Specific Effects of Stress on Oxytocin Neurons Correspond With Responses to Intranasal Oxytocin', Biological Psychiatry, vol. 80, no. 5, pp. 406-414. https://doi.org/10.1016/j.biopsych.2015.10.007
Steinman, Michael Q. ; Duque-Wilckens, Natalia ; Greenberg, Gian D. ; Hao, Rebecca ; Campi, Katharine L. ; Laredo, Sarah A. ; Laman-Maharg, Abigail ; Manning, Claire E. ; Doig, Ian E. ; Lopez, Eduardo M. ; Walch, Keenan ; Bales, Karen L. ; Trainor, Brian C. / Sex-Specific Effects of Stress on Oxytocin Neurons Correspond With Responses to Intranasal Oxytocin. In: Biological Psychiatry. 2016 ; Vol. 80, No. 5. pp. 406-414.
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abstract = "Background Oxytocin (OT) is considered to be a stress-buffering hormone, dampening the physiologic effects of stress. However, OT can also be anxiogenic. We examined acute and long-lasting effects of social defeat on OT neurons in male and female California mice. Methods We used immunohistochemistry for OT and c-fos cells to examine OT neuron activity immediately after defeat (n = 6–9) and 2 weeks (n = 6–9) and 10 weeks (n = 4–5) later. We quantified Oxt messenger RNA with quantitative polymerase chain reaction (n = 5–9). Intranasal OT was administered to na{\"i}ve and stressed mice tested in social interaction and resident-intruder tests (n = 8–14). Results Acute exposure to a third episode of defeat increased OT/c-fos colocalizations in the paraventricular nucleus of both sexes. In the medioventral bed nucleus of the stria terminalis, defeat increased Oxt messenger RNA, total OT neurons, and OT/c-fos colocalizations in female mice but not male mice. Intranasal OT failed to reverse stress-induced social withdrawal in female mice and reduced social interaction behavior in female mice na{\"i}ve to defeat. In contrast, intranasal OT increased social interaction in stressed male mice and reduced freezing in the resident-intruder test. Conclusions Social defeat induces long-lasting increases in OT production and OT/c-fos cells in the medioventral bed nucleus of the stria terminalis of female mice but not male mice. Intranasal OT largely reversed the effects of stress on behavior in male mice, but effects were mixed in female mice. These results suggest that changes in OT-sensitive networks contribute to sex differences in behavioral responses to stress.",
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AU - Hao, Rebecca

AU - Campi, Katharine L.

AU - Laredo, Sarah A.

AU - Laman-Maharg, Abigail

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AU - Doig, Ian E.

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KW - Peromyscus

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