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Late Pregnancy is a Critical Period for Changes in Phosphorylated Mitogen‐Activated Protein Kinase/Extracellular Signal‐Regulated Kinase 1/2 in Oxytocin Neurones

The physiological demands of parturition and lactation lead to the increased pulsatile release of oxytocin (OT) into the circulation from the neurohypophysial axons of OT neurones in the supraoptic (SON) and paraventricular (PVN) nuclei. These states of increased OT release are accompanied by a sign...

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Autores principales: Chandaka, G. K., Wang, L., Senogles, S., Armstrong, W. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028259/
https://www.ncbi.nlm.nih.gov/pubmed/27203238
http://dx.doi.org/10.1111/jne.12398
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author Chandaka, G. K.
Wang, L.
Senogles, S.
Armstrong, W. E.
author_facet Chandaka, G. K.
Wang, L.
Senogles, S.
Armstrong, W. E.
author_sort Chandaka, G. K.
collection PubMed
description The physiological demands of parturition and lactation lead to the increased pulsatile release of oxytocin (OT) into the circulation from the neurohypophysial axons of OT neurones in the supraoptic (SON) and paraventricular (PVN) nuclei. These states of increased OT release are accompanied by a significant plasticity in magnocellular OT neurones and their synaptic connections, and many of these changes require activation of a central OT receptor. The mitogen‐activated protein kinase/extracellular signal‐regulated kinase pathway (MAPK/ERK) is assumed to be up‐regulated in the PVN during lactation, and many of the effects of OT in peripheral and brain tissue are mediated through a MAPK/ERK pathway. The present study investigated whether this pathway is altered in the SON and PVN during late pregnancy [embryonic day (E)20–21], which is a critical period for OT plasticity induction, and for lactation, when plastic changes are sustained. Based on immunoreactivity for phosphorylated ERK1/2 (pERK1/2), the results suggest an enhanced activation of MAPK/ERK pathway in OT neurones specifically during late pregnancy in both the SON and PVN. Although immunoblots from the SON confirm this pregnancy‐associated up‐regulation in late pregnancy, they also suggest enhancement into lactation as well. Together, the results suggest an important role for the MAPK/ERK pathway during reproductive changes in the SON and PVN.
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spelling pubmed-50282592016-11-09 Late Pregnancy is a Critical Period for Changes in Phosphorylated Mitogen‐Activated Protein Kinase/Extracellular Signal‐Regulated Kinase 1/2 in Oxytocin Neurones Chandaka, G. K. Wang, L. Senogles, S. Armstrong, W. E. J Neuroendocrinol Original Articles The physiological demands of parturition and lactation lead to the increased pulsatile release of oxytocin (OT) into the circulation from the neurohypophysial axons of OT neurones in the supraoptic (SON) and paraventricular (PVN) nuclei. These states of increased OT release are accompanied by a significant plasticity in magnocellular OT neurones and their synaptic connections, and many of these changes require activation of a central OT receptor. The mitogen‐activated protein kinase/extracellular signal‐regulated kinase pathway (MAPK/ERK) is assumed to be up‐regulated in the PVN during lactation, and many of the effects of OT in peripheral and brain tissue are mediated through a MAPK/ERK pathway. The present study investigated whether this pathway is altered in the SON and PVN during late pregnancy [embryonic day (E)20–21], which is a critical period for OT plasticity induction, and for lactation, when plastic changes are sustained. Based on immunoreactivity for phosphorylated ERK1/2 (pERK1/2), the results suggest an enhanced activation of MAPK/ERK pathway in OT neurones specifically during late pregnancy in both the SON and PVN. Although immunoblots from the SON confirm this pregnancy‐associated up‐regulation in late pregnancy, they also suggest enhancement into lactation as well. Together, the results suggest an important role for the MAPK/ERK pathway during reproductive changes in the SON and PVN. John Wiley and Sons Inc. 2016-08-19 2016-09 /pmc/articles/PMC5028259/ /pubmed/27203238 http://dx.doi.org/10.1111/jne.12398 Text en © 2016 The Authors. Journal of Neuroendocrinology published by John Wiley & Sons Ltd on behalf of British Society for Neuroendocrinology. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Chandaka, G. K.
Wang, L.
Senogles, S.
Armstrong, W. E.
Late Pregnancy is a Critical Period for Changes in Phosphorylated Mitogen‐Activated Protein Kinase/Extracellular Signal‐Regulated Kinase 1/2 in Oxytocin Neurones
title Late Pregnancy is a Critical Period for Changes in Phosphorylated Mitogen‐Activated Protein Kinase/Extracellular Signal‐Regulated Kinase 1/2 in Oxytocin Neurones
title_full Late Pregnancy is a Critical Period for Changes in Phosphorylated Mitogen‐Activated Protein Kinase/Extracellular Signal‐Regulated Kinase 1/2 in Oxytocin Neurones
title_fullStr Late Pregnancy is a Critical Period for Changes in Phosphorylated Mitogen‐Activated Protein Kinase/Extracellular Signal‐Regulated Kinase 1/2 in Oxytocin Neurones
title_full_unstemmed Late Pregnancy is a Critical Period for Changes in Phosphorylated Mitogen‐Activated Protein Kinase/Extracellular Signal‐Regulated Kinase 1/2 in Oxytocin Neurones
title_short Late Pregnancy is a Critical Period for Changes in Phosphorylated Mitogen‐Activated Protein Kinase/Extracellular Signal‐Regulated Kinase 1/2 in Oxytocin Neurones
title_sort late pregnancy is a critical period for changes in phosphorylated mitogen‐activated protein kinase/extracellular signal‐regulated kinase 1/2 in oxytocin neurones
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028259/
https://www.ncbi.nlm.nih.gov/pubmed/27203238
http://dx.doi.org/10.1111/jne.12398
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