Distribution of vasopressin 1a and oxytocin receptor protein and mRNA in the basal forebrain and midbrain of the spiny mouse (Acomys cahirinus)

Jeanne M. Powell, Kiyoshi Inoue, Kelly J. Wallace, Ashley W. Seifert, Larry J. Young, Aubrey M. Kelly

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

The nonapeptide system modulates numerous social behaviors through oxytocin and vasopressin activation of the oxytocin receptor (OXTR) and vasopressin receptor (AVPR1A) in the brain. OXTRs and AVPR1As are widely distributed throughout the brain and binding densities exhibit substantial variation within and across species. Although OXTR and AVPR1A binding distributions have been mapped for several rodents, this system has yet to be characterized in the spiny mouse (Acomys cahirinus). Here we conducted receptor autoradiography and in situ hybridization to map distributions of OXTR and AVPR1A binding and Oxtr and Avpr1a mRNA expression throughout the basal forebrain and midbrain of male and female spiny mice. We found that nonapeptide receptor mRNA is diffuse throughout the forebrain and midbrain and does not always align with OXTR and AVPR1A binding. Analyses of sex differences in brain regions involved in social behavior and reward revealed that males exhibit higher OXTR binding densities in the lateral septum, bed nucleus of the stria terminalis, and anterior hypothalamus. However, no association with gonadal sex was observed for AVPR1A binding. Hierarchical clustering analysis further revealed that co-expression patterns of OXTR and AVPR1A binding across brain regions involved in social behavior and reward differ between males and females. These findings provide mapping distributions and sex differences in nonapeptide receptors in spiny mice. Spiny mice are an excellent organism for studying grouping behaviors such as cooperation and prosociality, and the nonapeptide receptor mapping here can inform the study of nonapeptide-mediated behavior in a highly social, large group-living rodent.

Original languageEnglish
Pages (from-to)413-431
Number of pages19
JournalBrain Structure and Function
Volume228
Issue number2
DOIs
StatePublished - Mar 2023

Bibliographical note

Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Funding

We would like to acknowledge funding from the Esther A. and Joseph Klingenstein Fund (Klingenstein-Simons Fellowship Award in Neuroscience to AMK), the National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR070313 to AWS), the National Science Foundation (IOS-1353713 to AWS), and the National Institute of Mental Health (Emory CONTE Center Pilot Project Grant; P50MH100023 to LJY and P51OD11132 to Emory National Primate Research Center).

FundersFunder number
Center for Selective C-H Functionalization, National Science Foundation
Esther A. and Joseph Klingenstein Fund
Center for Hierarchical Manufacturing, National Science Foundation
Klingenstein-Simons Fellowship Award in Neuroscience
Not added1353713
National Institute of Mental HealthP50MH100023, P51OD11132
National Institute of Arthritis and Musculoskeletal and Skin DiseasesR01AR070313

    Keywords

    • In situ hybridization
    • Oxytocin
    • Receptor autoradiography
    • Social behavior
    • Spiny mouses
    • Vasopressin

    ASJC Scopus subject areas

    • Anatomy
    • General Neuroscience
    • Histology

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