Early neonatal echocardiographic findings in an experimental rabbit model of congenital diaphragmatic hernia

This study aimed to demonstrate that congenital diaphragmatic hernia (CDH) results in vascular abnormalities that are directly associated with the severity of pulmonary hypoplasia and hypertension. These events increase right ventricle (RV) afterload and may adversely affect disease management and p...

Full description

Bibliographic Details
Main Authors: P.H. Manso, R.L. Figueira, C.M. Prado, F.L. Gonçalves, A.L.B. Simões, S.G. Ramos, L. Sbragia
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2015-03-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2015000300234&lng=en&tlng=en
_version_ 1818720250343981056
author P.H. Manso
R.L. Figueira
C.M. Prado
F.L. Gonçalves
A.L.B. Simões
S.G. Ramos
L. Sbragia
author_facet P.H. Manso
R.L. Figueira
C.M. Prado
F.L. Gonçalves
A.L.B. Simões
S.G. Ramos
L. Sbragia
author_sort P.H. Manso
collection DOAJ
description This study aimed to demonstrate that congenital diaphragmatic hernia (CDH) results in vascular abnormalities that are directly associated with the severity of pulmonary hypoplasia and hypertension. These events increase right ventricle (RV) afterload and may adversely affect disease management and patient survival. Our objective was to investigate cardiac function, specifically right ventricular changes, immediately after birth and relate them to myocardial histological findings in a CDH model. Pregnant New Zealand rabbits underwent the surgical procedure at 25 days of gestation (n=14). CDH was created in one fetus per horn (n=16), and the other fetuses were used as controls (n=20). At term (30 days), fetuses were removed, immediately dried and weighed before undergoing four-parameter echocardiography. The lungs and the heart were removed, weighed, and histologically analyzed. CDH animals had smaller total lung weight (P<0.005), left lung weight (P<0.005), and lung-to-body ratio (P<0.005). Echocardiography revealed a smaller left-to-right ventricle ratio (LV/RV, P<0.005) and larger diastolic right ventricle size (DRVS, P<0.007). Histologic analysis revealed a larger number of myocytes undergoing mitotic division (186 vs 132, P<0.05) in CDH hearts. Immediate RV dilation of CDH hearts is related to myocyte mitosis increase. This information may aid the design of future strategies to address pulmonary hypertension in CDH.
first_indexed 2024-12-17T20:19:51Z
format Article
id doaj.art-4f2114d0c9e049a5a07eb5811bcda360
institution Directory Open Access Journal
issn 1414-431X
language English
last_indexed 2024-12-17T20:19:51Z
publishDate 2015-03-01
publisher Associação Brasileira de Divulgação Científica
record_format Article
series Brazilian Journal of Medical and Biological Research
spelling doaj.art-4f2114d0c9e049a5a07eb5811bcda3602022-12-21T21:33:58ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research1414-431X2015-03-0148323423910.1590/1414-431X20144184S0100-879X2015000300234Early neonatal echocardiographic findings in an experimental rabbit model of congenital diaphragmatic herniaP.H. MansoR.L. FigueiraC.M. PradoF.L. GonçalvesA.L.B. SimõesS.G. RamosL. SbragiaThis study aimed to demonstrate that congenital diaphragmatic hernia (CDH) results in vascular abnormalities that are directly associated with the severity of pulmonary hypoplasia and hypertension. These events increase right ventricle (RV) afterload and may adversely affect disease management and patient survival. Our objective was to investigate cardiac function, specifically right ventricular changes, immediately after birth and relate them to myocardial histological findings in a CDH model. Pregnant New Zealand rabbits underwent the surgical procedure at 25 days of gestation (n=14). CDH was created in one fetus per horn (n=16), and the other fetuses were used as controls (n=20). At term (30 days), fetuses were removed, immediately dried and weighed before undergoing four-parameter echocardiography. The lungs and the heart were removed, weighed, and histologically analyzed. CDH animals had smaller total lung weight (P<0.005), left lung weight (P<0.005), and lung-to-body ratio (P<0.005). Echocardiography revealed a smaller left-to-right ventricle ratio (LV/RV, P<0.005) and larger diastolic right ventricle size (DRVS, P<0.007). Histologic analysis revealed a larger number of myocytes undergoing mitotic division (186 vs 132, P<0.05) in CDH hearts. Immediate RV dilation of CDH hearts is related to myocyte mitosis increase. This information may aid the design of future strategies to address pulmonary hypertension in CDH.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2015000300234&lng=en&tlng=enCongenital diaphragmatic herniaRight ventriclePulmonary arterial hypertensionEchocardiography
spellingShingle P.H. Manso
R.L. Figueira
C.M. Prado
F.L. Gonçalves
A.L.B. Simões
S.G. Ramos
L. Sbragia
Early neonatal echocardiographic findings in an experimental rabbit model of congenital diaphragmatic hernia
Brazilian Journal of Medical and Biological Research
Congenital diaphragmatic hernia
Right ventricle
Pulmonary arterial hypertension
Echocardiography
title Early neonatal echocardiographic findings in an experimental rabbit model of congenital diaphragmatic hernia
title_full Early neonatal echocardiographic findings in an experimental rabbit model of congenital diaphragmatic hernia
title_fullStr Early neonatal echocardiographic findings in an experimental rabbit model of congenital diaphragmatic hernia
title_full_unstemmed Early neonatal echocardiographic findings in an experimental rabbit model of congenital diaphragmatic hernia
title_short Early neonatal echocardiographic findings in an experimental rabbit model of congenital diaphragmatic hernia
title_sort early neonatal echocardiographic findings in an experimental rabbit model of congenital diaphragmatic hernia
topic Congenital diaphragmatic hernia
Right ventricle
Pulmonary arterial hypertension
Echocardiography
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2015000300234&lng=en&tlng=en
work_keys_str_mv AT phmanso earlyneonatalechocardiographicfindingsinanexperimentalrabbitmodelofcongenitaldiaphragmatichernia
AT rlfigueira earlyneonatalechocardiographicfindingsinanexperimentalrabbitmodelofcongenitaldiaphragmatichernia
AT cmprado earlyneonatalechocardiographicfindingsinanexperimentalrabbitmodelofcongenitaldiaphragmatichernia
AT flgoncalves earlyneonatalechocardiographicfindingsinanexperimentalrabbitmodelofcongenitaldiaphragmatichernia
AT albsimoes earlyneonatalechocardiographicfindingsinanexperimentalrabbitmodelofcongenitaldiaphragmatichernia
AT sgramos earlyneonatalechocardiographicfindingsinanexperimentalrabbitmodelofcongenitaldiaphragmatichernia
AT lsbragia earlyneonatalechocardiographicfindingsinanexperimentalrabbitmodelofcongenitaldiaphragmatichernia