Cargando…

GnRH Neurons Provide Direct Input to Hypothalamic Tyrosine Hydroxylase Immunoreactive Neurons Which Is Maintained During Lactation

Gonadotropin releasing hormone (GnRH) neurons provide neuronal input to the preoptic area (POA) and the arcuate nucleus (Arc), two regions involved critically in the regulation of neuroendocrine functions and associated behaviors. These areas contain tyrosine hydroxylase immunoreactive (TH-IR) neuro...

Descripción completa

Detalles Bibliográficos
Autores principales: Bardóczi, Zsuzsanna, Wilheim, Tamás, Skrapits, Katalin, Hrabovszky, Erik, Rácz, Gergely, Matolcsy, András, Liposits, Zsolt, Sliwowska, Joanna H., Dobolyi, Árpád, Kalló, Imre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261975/
https://www.ncbi.nlm.nih.gov/pubmed/30524376
http://dx.doi.org/10.3389/fendo.2018.00685
_version_ 1783375016849571840
author Bardóczi, Zsuzsanna
Wilheim, Tamás
Skrapits, Katalin
Hrabovszky, Erik
Rácz, Gergely
Matolcsy, András
Liposits, Zsolt
Sliwowska, Joanna H.
Dobolyi, Árpád
Kalló, Imre
author_facet Bardóczi, Zsuzsanna
Wilheim, Tamás
Skrapits, Katalin
Hrabovszky, Erik
Rácz, Gergely
Matolcsy, András
Liposits, Zsolt
Sliwowska, Joanna H.
Dobolyi, Árpád
Kalló, Imre
author_sort Bardóczi, Zsuzsanna
collection PubMed
description Gonadotropin releasing hormone (GnRH) neurons provide neuronal input to the preoptic area (POA) and the arcuate nucleus (Arc), two regions involved critically in the regulation of neuroendocrine functions and associated behaviors. These areas contain tyrosine hydroxylase immunoreactive (TH-IR) neurons, which play location-specific roles in the neuroendocrine control of both the luteinizing hormone and prolactin secretion, as well as, sexually motivated behaviors. Concerning changes in the activity of GnRH neurons and the secretion pattern of GnRH seen under the influence of rising serum estrogen levels and during lactation, we tested the hypothesis that the functional state of GnRH neurons is mediated via direct synaptic connections to TH-IR neurons in the POA and Arc. In addition, we examined putative changes of these inputs in lactating mice and in mothers separated from their pups. Confocal microscopic and pre-embedding immunohistochemical studies on ovariectomized mice treated with 17β-estradiol (OVX+E2) provided evidence for direct appositions and asymmetric synapses between GnRH-IR fiber varicosities and TH-IR neurons in the POA and the Arc. As TH co-localizes with kisspeptin (KP) in the POA, confocal microscopic analysis was continued on sections additionally labeled for KP. The TH-IR neurons showed a lower level of co-labeling for KP in lactating mice compared to OVX+E2 mice (16.1 ± 5% vs. 57.8 ± 4.3%). Removing the pups for 24 h did not alter significantly the KP production in TH-IR neurons (17.3 ± 4.6%). The mean number of GnRH-IR varicosities on preoptic and arcuate TH cells did not differ in the three animal models investigated. This study shows evidence that GnRH neurons provide direct synaptic inputs to POA and Arc dopaminergic neurons. The scale of anatomical connectivity with these target cells was unaltered during lactation indicating a maintained GnRH input, inspite of the altered hormonal condition.
format Online
Article
Text
id pubmed-6261975
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-62619752018-12-06 GnRH Neurons Provide Direct Input to Hypothalamic Tyrosine Hydroxylase Immunoreactive Neurons Which Is Maintained During Lactation Bardóczi, Zsuzsanna Wilheim, Tamás Skrapits, Katalin Hrabovszky, Erik Rácz, Gergely Matolcsy, András Liposits, Zsolt Sliwowska, Joanna H. Dobolyi, Árpád Kalló, Imre Front Endocrinol (Lausanne) Endocrinology Gonadotropin releasing hormone (GnRH) neurons provide neuronal input to the preoptic area (POA) and the arcuate nucleus (Arc), two regions involved critically in the regulation of neuroendocrine functions and associated behaviors. These areas contain tyrosine hydroxylase immunoreactive (TH-IR) neurons, which play location-specific roles in the neuroendocrine control of both the luteinizing hormone and prolactin secretion, as well as, sexually motivated behaviors. Concerning changes in the activity of GnRH neurons and the secretion pattern of GnRH seen under the influence of rising serum estrogen levels and during lactation, we tested the hypothesis that the functional state of GnRH neurons is mediated via direct synaptic connections to TH-IR neurons in the POA and Arc. In addition, we examined putative changes of these inputs in lactating mice and in mothers separated from their pups. Confocal microscopic and pre-embedding immunohistochemical studies on ovariectomized mice treated with 17β-estradiol (OVX+E2) provided evidence for direct appositions and asymmetric synapses between GnRH-IR fiber varicosities and TH-IR neurons in the POA and the Arc. As TH co-localizes with kisspeptin (KP) in the POA, confocal microscopic analysis was continued on sections additionally labeled for KP. The TH-IR neurons showed a lower level of co-labeling for KP in lactating mice compared to OVX+E2 mice (16.1 ± 5% vs. 57.8 ± 4.3%). Removing the pups for 24 h did not alter significantly the KP production in TH-IR neurons (17.3 ± 4.6%). The mean number of GnRH-IR varicosities on preoptic and arcuate TH cells did not differ in the three animal models investigated. This study shows evidence that GnRH neurons provide direct synaptic inputs to POA and Arc dopaminergic neurons. The scale of anatomical connectivity with these target cells was unaltered during lactation indicating a maintained GnRH input, inspite of the altered hormonal condition. Frontiers Media S.A. 2018-11-22 /pmc/articles/PMC6261975/ /pubmed/30524376 http://dx.doi.org/10.3389/fendo.2018.00685 Text en Copyright © 2018 Bardóczi, Wilheim, Skrapits, Hrabovszky, Rácz, Matolcsy, Liposits, Sliwowska, Dobolyi and Kalló. 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 Endocrinology
Bardóczi, Zsuzsanna
Wilheim, Tamás
Skrapits, Katalin
Hrabovszky, Erik
Rácz, Gergely
Matolcsy, András
Liposits, Zsolt
Sliwowska, Joanna H.
Dobolyi, Árpád
Kalló, Imre
GnRH Neurons Provide Direct Input to Hypothalamic Tyrosine Hydroxylase Immunoreactive Neurons Which Is Maintained During Lactation
title GnRH Neurons Provide Direct Input to Hypothalamic Tyrosine Hydroxylase Immunoreactive Neurons Which Is Maintained During Lactation
title_full GnRH Neurons Provide Direct Input to Hypothalamic Tyrosine Hydroxylase Immunoreactive Neurons Which Is Maintained During Lactation
title_fullStr GnRH Neurons Provide Direct Input to Hypothalamic Tyrosine Hydroxylase Immunoreactive Neurons Which Is Maintained During Lactation
title_full_unstemmed GnRH Neurons Provide Direct Input to Hypothalamic Tyrosine Hydroxylase Immunoreactive Neurons Which Is Maintained During Lactation
title_short GnRH Neurons Provide Direct Input to Hypothalamic Tyrosine Hydroxylase Immunoreactive Neurons Which Is Maintained During Lactation
title_sort gnrh neurons provide direct input to hypothalamic tyrosine hydroxylase immunoreactive neurons which is maintained during lactation
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261975/
https://www.ncbi.nlm.nih.gov/pubmed/30524376
http://dx.doi.org/10.3389/fendo.2018.00685
work_keys_str_mv AT bardoczizsuzsanna gnrhneuronsprovidedirectinputtohypothalamictyrosinehydroxylaseimmunoreactiveneuronswhichismaintainedduringlactation
AT wilheimtamas gnrhneuronsprovidedirectinputtohypothalamictyrosinehydroxylaseimmunoreactiveneuronswhichismaintainedduringlactation
AT skrapitskatalin gnrhneuronsprovidedirectinputtohypothalamictyrosinehydroxylaseimmunoreactiveneuronswhichismaintainedduringlactation
AT hrabovszkyerik gnrhneuronsprovidedirectinputtohypothalamictyrosinehydroxylaseimmunoreactiveneuronswhichismaintainedduringlactation
AT raczgergely gnrhneuronsprovidedirectinputtohypothalamictyrosinehydroxylaseimmunoreactiveneuronswhichismaintainedduringlactation
AT matolcsyandras gnrhneuronsprovidedirectinputtohypothalamictyrosinehydroxylaseimmunoreactiveneuronswhichismaintainedduringlactation
AT lipositszsolt gnrhneuronsprovidedirectinputtohypothalamictyrosinehydroxylaseimmunoreactiveneuronswhichismaintainedduringlactation
AT sliwowskajoannah gnrhneuronsprovidedirectinputtohypothalamictyrosinehydroxylaseimmunoreactiveneuronswhichismaintainedduringlactation
AT dobolyiarpad gnrhneuronsprovidedirectinputtohypothalamictyrosinehydroxylaseimmunoreactiveneuronswhichismaintainedduringlactation
AT kalloimre gnrhneuronsprovidedirectinputtohypothalamictyrosinehydroxylaseimmunoreactiveneuronswhichismaintainedduringlactation