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Relaxin-3 Innervation From the Nucleus Incertus to the Parahippocampal Cortex of the Rat

Spatial learning and memory processes depend on anatomical and functional interactions between the hippocampus and the entorhinal cortex. A key neurophysiological component of these processes is hippocampal theta rhythm, which can be driven from subcortical areas including the pontine nucleus incert...

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Autores principales: García-Díaz, Cristina, Gil-Miravet, Isis, Albert-Gasco, Hector, Mañas-Ojeda, Aroa, Ros-Bernal, Francisco, Castillo-Gómez, Esther, Gundlach, Andrew L., Olucha-Bordonau, Francisco E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258164/
https://www.ncbi.nlm.nih.gov/pubmed/34239421
http://dx.doi.org/10.3389/fnana.2021.674649
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author García-Díaz, Cristina
Gil-Miravet, Isis
Albert-Gasco, Hector
Mañas-Ojeda, Aroa
Ros-Bernal, Francisco
Castillo-Gómez, Esther
Gundlach, Andrew L.
Olucha-Bordonau, Francisco E.
author_facet García-Díaz, Cristina
Gil-Miravet, Isis
Albert-Gasco, Hector
Mañas-Ojeda, Aroa
Ros-Bernal, Francisco
Castillo-Gómez, Esther
Gundlach, Andrew L.
Olucha-Bordonau, Francisco E.
author_sort García-Díaz, Cristina
collection PubMed
description Spatial learning and memory processes depend on anatomical and functional interactions between the hippocampus and the entorhinal cortex. A key neurophysiological component of these processes is hippocampal theta rhythm, which can be driven from subcortical areas including the pontine nucleus incertus (NI). The NI contains the largest population of neurons that produce and presumably release the neuropeptide, relaxin-3, which acts via the G(i/o)-protein-coupled receptor, relaxin-family peptide 3 receptor (RXFP3). NI activation induces general arousal including hippocampal theta, and inactivation induces impairment of spatial memory acquisition or retrieval. The primary aim of this study was to map the NI/relaxin-3 innervation of the parahippocampal cortex (PHC), including the medial and lateral entorhinal cortex, endopiriform cortex, perirhinal, postrhinal, and ectorhinal cortex, the amygdalohippocampal transition area and posteromedial cortical amygdala. Retrograde tracer injections were placed in different parts of the medial and lateral entorhinal cortex, which produced prominent retrograde labeling in the ipsilateral NI and some labeling in the contralateral NI. Anterograde tracer injections into the NI and immunostaining for relaxin-3 produced fiber labeling in deep layers of all parahippocampal areas and some dispersed fibers in superficial layers. Double-labeling studies revealed that both hippocampal projecting and calcium-binding protein-positive (presumed GABAergic) neurons received a relaxin-3 NI innervation. Some of these fibers also displayed synaptophysin (Syn) immunoreactivity, consistent with the presence of the peptide at synapses; and relaxin-3-positive fibers containing Syn bouton-like staining were frequently observed in contact with hippocampal-projecting or calcium-binding protein-positive neuronal somata and more distal elements. Finally, in situ hybridization studies revealed that entorhinal neurons in the superficial layers, and to a lesser extent in deep layers, contain RXFP3 mRNA. Together, our data support functional actions of the NI/relaxin-3-parahippocampal innervation on processes related to memory, spatial navigation and contextual analysis.
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spelling pubmed-82581642021-07-07 Relaxin-3 Innervation From the Nucleus Incertus to the Parahippocampal Cortex of the Rat García-Díaz, Cristina Gil-Miravet, Isis Albert-Gasco, Hector Mañas-Ojeda, Aroa Ros-Bernal, Francisco Castillo-Gómez, Esther Gundlach, Andrew L. Olucha-Bordonau, Francisco E. Front Neuroanat Neuroanatomy Spatial learning and memory processes depend on anatomical and functional interactions between the hippocampus and the entorhinal cortex. A key neurophysiological component of these processes is hippocampal theta rhythm, which can be driven from subcortical areas including the pontine nucleus incertus (NI). The NI contains the largest population of neurons that produce and presumably release the neuropeptide, relaxin-3, which acts via the G(i/o)-protein-coupled receptor, relaxin-family peptide 3 receptor (RXFP3). NI activation induces general arousal including hippocampal theta, and inactivation induces impairment of spatial memory acquisition or retrieval. The primary aim of this study was to map the NI/relaxin-3 innervation of the parahippocampal cortex (PHC), including the medial and lateral entorhinal cortex, endopiriform cortex, perirhinal, postrhinal, and ectorhinal cortex, the amygdalohippocampal transition area and posteromedial cortical amygdala. Retrograde tracer injections were placed in different parts of the medial and lateral entorhinal cortex, which produced prominent retrograde labeling in the ipsilateral NI and some labeling in the contralateral NI. Anterograde tracer injections into the NI and immunostaining for relaxin-3 produced fiber labeling in deep layers of all parahippocampal areas and some dispersed fibers in superficial layers. Double-labeling studies revealed that both hippocampal projecting and calcium-binding protein-positive (presumed GABAergic) neurons received a relaxin-3 NI innervation. Some of these fibers also displayed synaptophysin (Syn) immunoreactivity, consistent with the presence of the peptide at synapses; and relaxin-3-positive fibers containing Syn bouton-like staining were frequently observed in contact with hippocampal-projecting or calcium-binding protein-positive neuronal somata and more distal elements. Finally, in situ hybridization studies revealed that entorhinal neurons in the superficial layers, and to a lesser extent in deep layers, contain RXFP3 mRNA. Together, our data support functional actions of the NI/relaxin-3-parahippocampal innervation on processes related to memory, spatial navigation and contextual analysis. Frontiers Media S.A. 2021-06-22 /pmc/articles/PMC8258164/ /pubmed/34239421 http://dx.doi.org/10.3389/fnana.2021.674649 Text en Copyright © 2021 García-Díaz, Gil-Miravet, Albert-Gasco, Mañas-Ojeda, Ros-Bernal, Castillo-Gómez, Gundlach and Olucha-Bordonau. https://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 Neuroanatomy
García-Díaz, Cristina
Gil-Miravet, Isis
Albert-Gasco, Hector
Mañas-Ojeda, Aroa
Ros-Bernal, Francisco
Castillo-Gómez, Esther
Gundlach, Andrew L.
Olucha-Bordonau, Francisco E.
Relaxin-3 Innervation From the Nucleus Incertus to the Parahippocampal Cortex of the Rat
title Relaxin-3 Innervation From the Nucleus Incertus to the Parahippocampal Cortex of the Rat
title_full Relaxin-3 Innervation From the Nucleus Incertus to the Parahippocampal Cortex of the Rat
title_fullStr Relaxin-3 Innervation From the Nucleus Incertus to the Parahippocampal Cortex of the Rat
title_full_unstemmed Relaxin-3 Innervation From the Nucleus Incertus to the Parahippocampal Cortex of the Rat
title_short Relaxin-3 Innervation From the Nucleus Incertus to the Parahippocampal Cortex of the Rat
title_sort relaxin-3 innervation from the nucleus incertus to the parahippocampal cortex of the rat
topic Neuroanatomy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258164/
https://www.ncbi.nlm.nih.gov/pubmed/34239421
http://dx.doi.org/10.3389/fnana.2021.674649
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