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HLHS: Power of the Chick Model

Background: Hypoplastic left heart syndrome (HLHS) is a rare but deadly form of human congenital heart disease, most likely of diverse etiologies. Hemodynamic alterations such as those resulting from premature foramen ovale closure or aortic stenosis are among the possible pathways. Methods: The inf...

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Detalles Bibliográficos
Autor principal: Sedmera, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031965/
https://www.ncbi.nlm.nih.gov/pubmed/35448089
http://dx.doi.org/10.3390/jcdd9040113
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author Sedmera, David
author_facet Sedmera, David
author_sort Sedmera, David
collection PubMed
description Background: Hypoplastic left heart syndrome (HLHS) is a rare but deadly form of human congenital heart disease, most likely of diverse etiologies. Hemodynamic alterations such as those resulting from premature foramen ovale closure or aortic stenosis are among the possible pathways. Methods: The information gained from studies performed in the chick model of HLHS is reviewed. Altered hemodynamics leads to a decrease in myocyte proliferation causing hypoplasia of the left heart structures and their functional changes. Conclusions: Although the chick phenocopy of HLHS caused by left atrial ligation is certainly not representative of all the possible etiologies, it provides many useful hints regarding the plasticity of the genetically normal developing myocardium under altered hemodynamic loading leading to the HLHS phenotype, and even suggestions on some potential strategies for prenatal repair.
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spelling pubmed-90319652022-04-23 HLHS: Power of the Chick Model Sedmera, David J Cardiovasc Dev Dis Review Background: Hypoplastic left heart syndrome (HLHS) is a rare but deadly form of human congenital heart disease, most likely of diverse etiologies. Hemodynamic alterations such as those resulting from premature foramen ovale closure or aortic stenosis are among the possible pathways. Methods: The information gained from studies performed in the chick model of HLHS is reviewed. Altered hemodynamics leads to a decrease in myocyte proliferation causing hypoplasia of the left heart structures and their functional changes. Conclusions: Although the chick phenocopy of HLHS caused by left atrial ligation is certainly not representative of all the possible etiologies, it provides many useful hints regarding the plasticity of the genetically normal developing myocardium under altered hemodynamic loading leading to the HLHS phenotype, and even suggestions on some potential strategies for prenatal repair. MDPI 2022-04-11 /pmc/articles/PMC9031965/ /pubmed/35448089 http://dx.doi.org/10.3390/jcdd9040113 Text en © 2022 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sedmera, David
HLHS: Power of the Chick Model
title HLHS: Power of the Chick Model
title_full HLHS: Power of the Chick Model
title_fullStr HLHS: Power of the Chick Model
title_full_unstemmed HLHS: Power of the Chick Model
title_short HLHS: Power of the Chick Model
title_sort hlhs: power of the chick model
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031965/
https://www.ncbi.nlm.nih.gov/pubmed/35448089
http://dx.doi.org/10.3390/jcdd9040113
work_keys_str_mv AT sedmeradavid hlhspowerofthechickmodel