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Oxytocin Receptor Binding Sites in the Periphery of the Neonatal Prairie Vole

The oxytocin receptor (OXTR) has been observed in the periphery of neonatal C57BL/6J mice (Mus musculus), including facial regions and the anogenital area. In those studies, ligand specificity was confirmed with a congenital OXTR knockout mouse as well as competitive binding techniques. The aim of t...

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Autores principales: Greenwood, Maria A., Hammock, Elizabeth A. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542991/
https://www.ncbi.nlm.nih.gov/pubmed/31178680
http://dx.doi.org/10.3389/fnins.2019.00474
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author Greenwood, Maria A.
Hammock, Elizabeth A. D.
author_facet Greenwood, Maria A.
Hammock, Elizabeth A. D.
author_sort Greenwood, Maria A.
collection PubMed
description The oxytocin receptor (OXTR) has been observed in the periphery of neonatal C57BL/6J mice (Mus musculus), including facial regions and the anogenital area. In those studies, ligand specificity was confirmed with a congenital OXTR knockout mouse as well as competitive binding techniques. The aim of this study was to determine if OXTR is present in the same peripheral sites in the neonatal prairie vole (Microtus ochrogaster) for cross-species comparisons. Receptor autoradiography was performed on 20 μm sagittal sections of whole postnatal day 0 (P0) male and female prairie voles using the (125)iodinated-ornithine vasotocin ([(125)I]-OVTA) radioligand. A competition binding assay was used to assess the selectivity of [(125)I]-OVTA for peripheral OXTR. Radioactive ligand (0.05 nM [(125)I]-OVTA) was competed against concentrations of 0 and 1000 nM excess unlabeled oxytocin (OXT). Previously identified regions of significant OXTR ligand binding in the mouse were analyzed for comparison: rostral and lateral periodontium, olfactory epithelium, ciliary bodies of the eye, whisker pads, adrenal gland, and anogenital area. We also evaluated the liver and scapular brown adipose tissue, which displayed strong but non-specific signal on film in mice. While there were some areas that showed conserved OXTR ligand binding in the prairie vole (e.g., ciliary body of the eye and the anogenital area), areas showing OXTR ligand binding in the neonatal prairie vole were not identical to OXTR ligand binding in the periphery of the C57BL/6J neonatal mouse. Further, some of the regions measured in the prairie vole suggest sex differences in OXTR ligand binding. Collectively, as is well-established in the central nervous system, these data indicate that patterns of OXTR ligand binding in the infant periphery are species-specific.
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spelling pubmed-65429912019-06-07 Oxytocin Receptor Binding Sites in the Periphery of the Neonatal Prairie Vole Greenwood, Maria A. Hammock, Elizabeth A. D. Front Neurosci Neuroscience The oxytocin receptor (OXTR) has been observed in the periphery of neonatal C57BL/6J mice (Mus musculus), including facial regions and the anogenital area. In those studies, ligand specificity was confirmed with a congenital OXTR knockout mouse as well as competitive binding techniques. The aim of this study was to determine if OXTR is present in the same peripheral sites in the neonatal prairie vole (Microtus ochrogaster) for cross-species comparisons. Receptor autoradiography was performed on 20 μm sagittal sections of whole postnatal day 0 (P0) male and female prairie voles using the (125)iodinated-ornithine vasotocin ([(125)I]-OVTA) radioligand. A competition binding assay was used to assess the selectivity of [(125)I]-OVTA for peripheral OXTR. Radioactive ligand (0.05 nM [(125)I]-OVTA) was competed against concentrations of 0 and 1000 nM excess unlabeled oxytocin (OXT). Previously identified regions of significant OXTR ligand binding in the mouse were analyzed for comparison: rostral and lateral periodontium, olfactory epithelium, ciliary bodies of the eye, whisker pads, adrenal gland, and anogenital area. We also evaluated the liver and scapular brown adipose tissue, which displayed strong but non-specific signal on film in mice. While there were some areas that showed conserved OXTR ligand binding in the prairie vole (e.g., ciliary body of the eye and the anogenital area), areas showing OXTR ligand binding in the neonatal prairie vole were not identical to OXTR ligand binding in the periphery of the C57BL/6J neonatal mouse. Further, some of the regions measured in the prairie vole suggest sex differences in OXTR ligand binding. Collectively, as is well-established in the central nervous system, these data indicate that patterns of OXTR ligand binding in the infant periphery are species-specific. Frontiers Media S.A. 2019-05-24 /pmc/articles/PMC6542991/ /pubmed/31178680 http://dx.doi.org/10.3389/fnins.2019.00474 Text en Copyright © 2019 Greenwood and Hammock. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Greenwood, Maria A.
Hammock, Elizabeth A. D.
Oxytocin Receptor Binding Sites in the Periphery of the Neonatal Prairie Vole
title Oxytocin Receptor Binding Sites in the Periphery of the Neonatal Prairie Vole
title_full Oxytocin Receptor Binding Sites in the Periphery of the Neonatal Prairie Vole
title_fullStr Oxytocin Receptor Binding Sites in the Periphery of the Neonatal Prairie Vole
title_full_unstemmed Oxytocin Receptor Binding Sites in the Periphery of the Neonatal Prairie Vole
title_short Oxytocin Receptor Binding Sites in the Periphery of the Neonatal Prairie Vole
title_sort oxytocin receptor binding sites in the periphery of the neonatal prairie vole
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542991/
https://www.ncbi.nlm.nih.gov/pubmed/31178680
http://dx.doi.org/10.3389/fnins.2019.00474
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