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Metabolic Changes Precede the Development of Pulmonary Hypertension in the Monocrotaline Exposed Rat Lung
There is increasing interest in the potential for metabolic profiling to evaluate the progression of pulmonary hypertension (PH). However, a detailed analysis of the metabolic changes in lungs at the early stage of PH, characterized by increased pulmonary artery pressure but prior to the development...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777490/ https://www.ncbi.nlm.nih.gov/pubmed/26937637 http://dx.doi.org/10.1371/journal.pone.0150480 |
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author | Rafikova, Olga Meadows, Mary L. Kinchen, Jason M. Mohney, Robert P. Maltepe, Emin Desai, Ankit A. Yuan, Jason X.-J. Garcia, Joe G. N. Fineman, Jeffrey R. Rafikov, Ruslan Black, Stephen M. |
author_facet | Rafikova, Olga Meadows, Mary L. Kinchen, Jason M. Mohney, Robert P. Maltepe, Emin Desai, Ankit A. Yuan, Jason X.-J. Garcia, Joe G. N. Fineman, Jeffrey R. Rafikov, Ruslan Black, Stephen M. |
author_sort | Rafikova, Olga |
collection | PubMed |
description | There is increasing interest in the potential for metabolic profiling to evaluate the progression of pulmonary hypertension (PH). However, a detailed analysis of the metabolic changes in lungs at the early stage of PH, characterized by increased pulmonary artery pressure but prior to the development of right ventricle hypertrophy and failure, is lacking in a preclinical animal model of PH. Thus, we undertook a study using rats 14 days after exposure to monocrotaline (MCT), to determine whether we could identify early stage metabolic changes prior to the manifestation of developed PH. We observed changes in multiple pathways associated with the development of PH, including activated glycolysis, increased markers of proliferation, disruptions in carnitine homeostasis, increased inflammatory and fibrosis biomarkers, and a reduction in glutathione biosynthesis. Further, our global metabolic profile data compare favorably with prior work carried out in humans with PH. We conclude that despite the MCT-model not recapitulating all the structural changes associated with humans with advanced PH, including endothelial cell proliferation and the formation of plexiform lesions, it is very similar at a metabolic level. Thus, we suggest that despite its limitations it can still serve as a useful preclinical model for the study of PH. |
format | Online Article Text |
id | pubmed-4777490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47774902016-03-10 Metabolic Changes Precede the Development of Pulmonary Hypertension in the Monocrotaline Exposed Rat Lung Rafikova, Olga Meadows, Mary L. Kinchen, Jason M. Mohney, Robert P. Maltepe, Emin Desai, Ankit A. Yuan, Jason X.-J. Garcia, Joe G. N. Fineman, Jeffrey R. Rafikov, Ruslan Black, Stephen M. PLoS One Research Article There is increasing interest in the potential for metabolic profiling to evaluate the progression of pulmonary hypertension (PH). However, a detailed analysis of the metabolic changes in lungs at the early stage of PH, characterized by increased pulmonary artery pressure but prior to the development of right ventricle hypertrophy and failure, is lacking in a preclinical animal model of PH. Thus, we undertook a study using rats 14 days after exposure to monocrotaline (MCT), to determine whether we could identify early stage metabolic changes prior to the manifestation of developed PH. We observed changes in multiple pathways associated with the development of PH, including activated glycolysis, increased markers of proliferation, disruptions in carnitine homeostasis, increased inflammatory and fibrosis biomarkers, and a reduction in glutathione biosynthesis. Further, our global metabolic profile data compare favorably with prior work carried out in humans with PH. We conclude that despite the MCT-model not recapitulating all the structural changes associated with humans with advanced PH, including endothelial cell proliferation and the formation of plexiform lesions, it is very similar at a metabolic level. Thus, we suggest that despite its limitations it can still serve as a useful preclinical model for the study of PH. Public Library of Science 2016-03-03 /pmc/articles/PMC4777490/ /pubmed/26937637 http://dx.doi.org/10.1371/journal.pone.0150480 Text en © 2016 Rafikova et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Rafikova, Olga Meadows, Mary L. Kinchen, Jason M. Mohney, Robert P. Maltepe, Emin Desai, Ankit A. Yuan, Jason X.-J. Garcia, Joe G. N. Fineman, Jeffrey R. Rafikov, Ruslan Black, Stephen M. Metabolic Changes Precede the Development of Pulmonary Hypertension in the Monocrotaline Exposed Rat Lung |
title | Metabolic Changes Precede the Development of Pulmonary Hypertension in the Monocrotaline Exposed Rat Lung |
title_full | Metabolic Changes Precede the Development of Pulmonary Hypertension in the Monocrotaline Exposed Rat Lung |
title_fullStr | Metabolic Changes Precede the Development of Pulmonary Hypertension in the Monocrotaline Exposed Rat Lung |
title_full_unstemmed | Metabolic Changes Precede the Development of Pulmonary Hypertension in the Monocrotaline Exposed Rat Lung |
title_short | Metabolic Changes Precede the Development of Pulmonary Hypertension in the Monocrotaline Exposed Rat Lung |
title_sort | metabolic changes precede the development of pulmonary hypertension in the monocrotaline exposed rat lung |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777490/ https://www.ncbi.nlm.nih.gov/pubmed/26937637 http://dx.doi.org/10.1371/journal.pone.0150480 |
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