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Nerve distribution in myocardium including the atrial and ventricular septa in late stage human fetuses

Few information had been reported on deep intracardiac nerves in the myocardium of late human fetuses such as nerves at the atrial-pulmonary vein junction and in the atrial and ventricular septa. We examined histological sections of the heart obtained from 12 human fetuses at 25–33 weeks. A high den...

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Autores principales: Cho, Kwang Ho, Kim, Ji Hyun, Murakami, Gen, Abe, Hiroshi, Rodríguez-Vázquez, José Francisco, Chai, Ok Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Anatomists 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449578/
https://www.ncbi.nlm.nih.gov/pubmed/30984452
http://dx.doi.org/10.5115/acb.2019.52.1.48
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author Cho, Kwang Ho
Kim, Ji Hyun
Murakami, Gen
Abe, Hiroshi
Rodríguez-Vázquez, José Francisco
Chai, Ok Hee
author_facet Cho, Kwang Ho
Kim, Ji Hyun
Murakami, Gen
Abe, Hiroshi
Rodríguez-Vázquez, José Francisco
Chai, Ok Hee
author_sort Cho, Kwang Ho
collection PubMed
description Few information had been reported on deep intracardiac nerves in the myocardium of late human fetuses such as nerves at the atrial-pulmonary vein junction and in the atrial and ventricular septa. We examined histological sections of the heart obtained from 12 human fetuses at 25–33 weeks. A high density of intracardiac nerves was evident around the mitral valve annulus in contrast to few nerves around the tricuspid annulus. To the crux at the atrioventricular sulcus, the degenerating left common cardinal vein brought abundant nerve bundles coming from cardiac nerves descending along the anterior aspect of the pulmonary trunk. Likewise, nerve bundles in the left atrial nerve fold came from cardiac nerves between the ascending aorta and pulmonary artery. Conversely, another nerves from the venous pole to the atrium seemed to be much limited in number. Moreover, the primary atrial septum contained much fewer nerves than the secondary septum. Therefore, nerve density in the atrial wall varied considerably between sites. As ventricular muscles were degenerated from the luminal side for sculpturing of papillary muscles and trabeculae, deep nerves became exposed to the ventricular endothelium. Likewise, as pectineal muscles were sculptured, nerves were exposed in the atrial endothelium. Consequently, a myocardial assembly or sculpture seemed to be associated with degeneration and reconstruction of early-developed nerves. A failure in reconstruction during further expansion of the left atrium might be connected with an individual variation in anatomical substrates of atrial fibrillation.
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spelling pubmed-64495782019-04-12 Nerve distribution in myocardium including the atrial and ventricular septa in late stage human fetuses Cho, Kwang Ho Kim, Ji Hyun Murakami, Gen Abe, Hiroshi Rodríguez-Vázquez, José Francisco Chai, Ok Hee Anat Cell Biol Original Article Few information had been reported on deep intracardiac nerves in the myocardium of late human fetuses such as nerves at the atrial-pulmonary vein junction and in the atrial and ventricular septa. We examined histological sections of the heart obtained from 12 human fetuses at 25–33 weeks. A high density of intracardiac nerves was evident around the mitral valve annulus in contrast to few nerves around the tricuspid annulus. To the crux at the atrioventricular sulcus, the degenerating left common cardinal vein brought abundant nerve bundles coming from cardiac nerves descending along the anterior aspect of the pulmonary trunk. Likewise, nerve bundles in the left atrial nerve fold came from cardiac nerves between the ascending aorta and pulmonary artery. Conversely, another nerves from the venous pole to the atrium seemed to be much limited in number. Moreover, the primary atrial septum contained much fewer nerves than the secondary septum. Therefore, nerve density in the atrial wall varied considerably between sites. As ventricular muscles were degenerated from the luminal side for sculpturing of papillary muscles and trabeculae, deep nerves became exposed to the ventricular endothelium. Likewise, as pectineal muscles were sculptured, nerves were exposed in the atrial endothelium. Consequently, a myocardial assembly or sculpture seemed to be associated with degeneration and reconstruction of early-developed nerves. A failure in reconstruction during further expansion of the left atrium might be connected with an individual variation in anatomical substrates of atrial fibrillation. Korean Association of Anatomists 2019-03 2019-03-29 /pmc/articles/PMC6449578/ /pubmed/30984452 http://dx.doi.org/10.5115/acb.2019.52.1.48 Text en Copyright © 2019. Anatomy & Cell Biology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Cho, Kwang Ho
Kim, Ji Hyun
Murakami, Gen
Abe, Hiroshi
Rodríguez-Vázquez, José Francisco
Chai, Ok Hee
Nerve distribution in myocardium including the atrial and ventricular septa in late stage human fetuses
title Nerve distribution in myocardium including the atrial and ventricular septa in late stage human fetuses
title_full Nerve distribution in myocardium including the atrial and ventricular septa in late stage human fetuses
title_fullStr Nerve distribution in myocardium including the atrial and ventricular septa in late stage human fetuses
title_full_unstemmed Nerve distribution in myocardium including the atrial and ventricular septa in late stage human fetuses
title_short Nerve distribution in myocardium including the atrial and ventricular septa in late stage human fetuses
title_sort nerve distribution in myocardium including the atrial and ventricular septa in late stage human fetuses
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449578/
https://www.ncbi.nlm.nih.gov/pubmed/30984452
http://dx.doi.org/10.5115/acb.2019.52.1.48
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