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Effect of bone marrow mesenchymal stem cells on experimental pulmonary arterial hypertension

The aim of the present study was to investigate the effect of bone marrow mesenchymal stem cell (BMSC) transp1antation on lung and heart damage in a rat model of monocrotaline (MCT)-induced pulmonary arterial hypertension (PAH). The animals were randomly divided into 3 groups: control, PAH and BMSC...

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Detalles Bibliográficos
Autores principales: ZHANG, ZHAO-HUA, LU, YAN, LUAN, YUN, ZHAO, JING-JIE
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493740/
https://www.ncbi.nlm.nih.gov/pubmed/23226736
http://dx.doi.org/10.3892/etm.2012.691
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author ZHANG, ZHAO-HUA
LU, YAN
LUAN, YUN
ZHAO, JING-JIE
author_facet ZHANG, ZHAO-HUA
LU, YAN
LUAN, YUN
ZHAO, JING-JIE
author_sort ZHANG, ZHAO-HUA
collection PubMed
description The aim of the present study was to investigate the effect of bone marrow mesenchymal stem cell (BMSC) transp1antation on lung and heart damage in a rat model of monocrotaline (MCT)-induced pulmonary arterial hypertension (PAH). The animals were randomly divided into 3 groups: control, PAH and BMSC implantation groups. Structural changes in the pulmonary vascular wall, such as the pulmonary artery lumen area (VA) and vascular area (TAA) were measured by hematoxylin and eosin (H&E) staining, and the hemodynamics were detected by echocardiography. Two weeks post-operation, our results demonstrated that sublingual vein injection of BMSCs significantly attenuated the pulmonary vascular structural and hemodynamic changes caused by pulmonary arterial hypertension. The mechanism may be executed via paracrine effects.
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spelling pubmed-34937402012-12-06 Effect of bone marrow mesenchymal stem cells on experimental pulmonary arterial hypertension ZHANG, ZHAO-HUA LU, YAN LUAN, YUN ZHAO, JING-JIE Exp Ther Med Articles The aim of the present study was to investigate the effect of bone marrow mesenchymal stem cell (BMSC) transp1antation on lung and heart damage in a rat model of monocrotaline (MCT)-induced pulmonary arterial hypertension (PAH). The animals were randomly divided into 3 groups: control, PAH and BMSC implantation groups. Structural changes in the pulmonary vascular wall, such as the pulmonary artery lumen area (VA) and vascular area (TAA) were measured by hematoxylin and eosin (H&E) staining, and the hemodynamics were detected by echocardiography. Two weeks post-operation, our results demonstrated that sublingual vein injection of BMSCs significantly attenuated the pulmonary vascular structural and hemodynamic changes caused by pulmonary arterial hypertension. The mechanism may be executed via paracrine effects. D.A. Spandidos 2012-11 2012-08-31 /pmc/articles/PMC3493740/ /pubmed/23226736 http://dx.doi.org/10.3892/etm.2012.691 Text en Copyright © 2012, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
ZHANG, ZHAO-HUA
LU, YAN
LUAN, YUN
ZHAO, JING-JIE
Effect of bone marrow mesenchymal stem cells on experimental pulmonary arterial hypertension
title Effect of bone marrow mesenchymal stem cells on experimental pulmonary arterial hypertension
title_full Effect of bone marrow mesenchymal stem cells on experimental pulmonary arterial hypertension
title_fullStr Effect of bone marrow mesenchymal stem cells on experimental pulmonary arterial hypertension
title_full_unstemmed Effect of bone marrow mesenchymal stem cells on experimental pulmonary arterial hypertension
title_short Effect of bone marrow mesenchymal stem cells on experimental pulmonary arterial hypertension
title_sort effect of bone marrow mesenchymal stem cells on experimental pulmonary arterial hypertension
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493740/
https://www.ncbi.nlm.nih.gov/pubmed/23226736
http://dx.doi.org/10.3892/etm.2012.691
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