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AVPR1A distribution in the whole C57BL/6J mouse neonate
The neuropeptide arginine vasopressin (AVP) plays significant roles in maintaining homeostasis and regulating social behavior. In vaginally delivered neonates, a surge of AVP is released into the bloodstream at levels exceeding release during life-threatening conditions such as hemorrhagic shock. It...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471960/ https://www.ncbi.nlm.nih.gov/pubmed/32884025 http://dx.doi.org/10.1038/s41598-020-71392-1 |
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author | Day, Katherine R. Coleman, Alexis Greenwood, Maria A. Hammock, Elizabeth A. D. |
author_facet | Day, Katherine R. Coleman, Alexis Greenwood, Maria A. Hammock, Elizabeth A. D. |
author_sort | Day, Katherine R. |
collection | PubMed |
description | The neuropeptide arginine vasopressin (AVP) plays significant roles in maintaining homeostasis and regulating social behavior. In vaginally delivered neonates, a surge of AVP is released into the bloodstream at levels exceeding release during life-threatening conditions such as hemorrhagic shock. It is currently unknown where the potential sites of action are in the neonate for these robust levels of circulating AVP at birth. The purpose of this study is to identify the location of AVP receptor 1a (AVPR1A) sites as potential peripheral targets of AVP in the neonatal mouse. RT-qPCR analysis of a sampling of tissues from the head demonstrated the presence of Avpr1a mRNA, suggesting local peripheral translation. Using competitive autoradiography in wildtype (WT) and AVPR1A knockout (KO) postnatal day 0 (P0) male and female mice on a C57BL/6J background, specific AVPR1A ligand binding was observed in the neonatal mouse periphery in sensory tissues of the head (eyes, ears, various oronasal regions), bone, spinal cord, adrenal cortex, and the uro-anogenital region in the neonatal AVPR1A WT mouse, as it was significantly reduced or absent in the control samples (AVPR1A KO and competition). AVPR1A throughout the neonatal periphery suggest roles for AVP in modulating peripheral physiology and development of the neonate. |
format | Online Article Text |
id | pubmed-7471960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74719602020-09-08 AVPR1A distribution in the whole C57BL/6J mouse neonate Day, Katherine R. Coleman, Alexis Greenwood, Maria A. Hammock, Elizabeth A. D. Sci Rep Article The neuropeptide arginine vasopressin (AVP) plays significant roles in maintaining homeostasis and regulating social behavior. In vaginally delivered neonates, a surge of AVP is released into the bloodstream at levels exceeding release during life-threatening conditions such as hemorrhagic shock. It is currently unknown where the potential sites of action are in the neonate for these robust levels of circulating AVP at birth. The purpose of this study is to identify the location of AVP receptor 1a (AVPR1A) sites as potential peripheral targets of AVP in the neonatal mouse. RT-qPCR analysis of a sampling of tissues from the head demonstrated the presence of Avpr1a mRNA, suggesting local peripheral translation. Using competitive autoradiography in wildtype (WT) and AVPR1A knockout (KO) postnatal day 0 (P0) male and female mice on a C57BL/6J background, specific AVPR1A ligand binding was observed in the neonatal mouse periphery in sensory tissues of the head (eyes, ears, various oronasal regions), bone, spinal cord, adrenal cortex, and the uro-anogenital region in the neonatal AVPR1A WT mouse, as it was significantly reduced or absent in the control samples (AVPR1A KO and competition). AVPR1A throughout the neonatal periphery suggest roles for AVP in modulating peripheral physiology and development of the neonate. Nature Publishing Group UK 2020-09-03 /pmc/articles/PMC7471960/ /pubmed/32884025 http://dx.doi.org/10.1038/s41598-020-71392-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Day, Katherine R. Coleman, Alexis Greenwood, Maria A. Hammock, Elizabeth A. D. AVPR1A distribution in the whole C57BL/6J mouse neonate |
title | AVPR1A distribution in the whole C57BL/6J mouse neonate |
title_full | AVPR1A distribution in the whole C57BL/6J mouse neonate |
title_fullStr | AVPR1A distribution in the whole C57BL/6J mouse neonate |
title_full_unstemmed | AVPR1A distribution in the whole C57BL/6J mouse neonate |
title_short | AVPR1A distribution in the whole C57BL/6J mouse neonate |
title_sort | avpr1a distribution in the whole c57bl/6j mouse neonate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471960/ https://www.ncbi.nlm.nih.gov/pubmed/32884025 http://dx.doi.org/10.1038/s41598-020-71392-1 |
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