Diaphragm atrophy and contractile dysfunction in a murine model of pulmonary hypertension.
Pulmonary hypertension (PH) causes loss of body weight and inspiratory (diaphragm) muscle dysfunction. A model of PH induced by drug (monocrotaline, MCT) has been extensively used in mice to examine the etiology of PH. However, it is unclear if PH induced by MCT in mice reproduces the loss of body w...
| Main Authors: | , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2013-01-01
|
| Series: | PLoS ONE |
| Online Access: | http://europepmc.org/articles/PMC3632558?pdf=render |
| _version_ | 1818194930256838656 |
|---|---|
| author | Bumsoo Ahn Hyacinth M Empinado Monsour Al-Rajhi Andrew R Judge Leonardo F Ferreira |
| author_facet | Bumsoo Ahn Hyacinth M Empinado Monsour Al-Rajhi Andrew R Judge Leonardo F Ferreira |
| author_sort | Bumsoo Ahn |
| collection | DOAJ |
| description | Pulmonary hypertension (PH) causes loss of body weight and inspiratory (diaphragm) muscle dysfunction. A model of PH induced by drug (monocrotaline, MCT) has been extensively used in mice to examine the etiology of PH. However, it is unclear if PH induced by MCT in mice reproduces the loss of body weight and diaphragm muscle dysfunction seen in patients. This is a pre-requisite for widespread use of mice to examine mechanisms of cachexia and diaphragm abnormalities in PH. Thus, we measured body and soleus muscle weight, food intake, and diaphragm contractile properties in mice after 6-8 weeks of saline (control) or MCT (600 mg/kg) injections. Body weight progressively decreased in PH mice, while food intake was similar in both groups. PH decreased (P<0.05) diaphragm maximal isometric specific force, maximal shortening velocity, and peak power. Protein carbonyls in whole-diaphragm lysates and the abundance of select myofibrillar proteins were unchanged by PH. Our findings show diaphragm isometric and isotonic contractile abnormalities in a murine model of PH induced by MCT. Overall, the murine model of PH elicited by MCT mimics loss of body weight and diaphragm muscle weakness reported in PH patients. |
| first_indexed | 2024-12-12T01:10:07Z |
| format | Article |
| id | doaj.art-5d696e7185104f53a0fb3e4ab41dae51 |
| institution | Directory Open Access Journal |
| issn | 1932-6203 |
| language | English |
| last_indexed | 2024-12-12T01:10:07Z |
| publishDate | 2013-01-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS ONE |
| spelling | doaj.art-5d696e7185104f53a0fb3e4ab41dae512022-12-22T00:43:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6270210.1371/journal.pone.0062702Diaphragm atrophy and contractile dysfunction in a murine model of pulmonary hypertension.Bumsoo AhnHyacinth M EmpinadoMonsour Al-RajhiAndrew R JudgeLeonardo F FerreiraPulmonary hypertension (PH) causes loss of body weight and inspiratory (diaphragm) muscle dysfunction. A model of PH induced by drug (monocrotaline, MCT) has been extensively used in mice to examine the etiology of PH. However, it is unclear if PH induced by MCT in mice reproduces the loss of body weight and diaphragm muscle dysfunction seen in patients. This is a pre-requisite for widespread use of mice to examine mechanisms of cachexia and diaphragm abnormalities in PH. Thus, we measured body and soleus muscle weight, food intake, and diaphragm contractile properties in mice after 6-8 weeks of saline (control) or MCT (600 mg/kg) injections. Body weight progressively decreased in PH mice, while food intake was similar in both groups. PH decreased (P<0.05) diaphragm maximal isometric specific force, maximal shortening velocity, and peak power. Protein carbonyls in whole-diaphragm lysates and the abundance of select myofibrillar proteins were unchanged by PH. Our findings show diaphragm isometric and isotonic contractile abnormalities in a murine model of PH induced by MCT. Overall, the murine model of PH elicited by MCT mimics loss of body weight and diaphragm muscle weakness reported in PH patients.http://europepmc.org/articles/PMC3632558?pdf=render |
| spellingShingle | Bumsoo Ahn Hyacinth M Empinado Monsour Al-Rajhi Andrew R Judge Leonardo F Ferreira Diaphragm atrophy and contractile dysfunction in a murine model of pulmonary hypertension. PLoS ONE |
| title | Diaphragm atrophy and contractile dysfunction in a murine model of pulmonary hypertension. |
| title_full | Diaphragm atrophy and contractile dysfunction in a murine model of pulmonary hypertension. |
| title_fullStr | Diaphragm atrophy and contractile dysfunction in a murine model of pulmonary hypertension. |
| title_full_unstemmed | Diaphragm atrophy and contractile dysfunction in a murine model of pulmonary hypertension. |
| title_short | Diaphragm atrophy and contractile dysfunction in a murine model of pulmonary hypertension. |
| title_sort | diaphragm atrophy and contractile dysfunction in a murine model of pulmonary hypertension |
| url | http://europepmc.org/articles/PMC3632558?pdf=render |
| work_keys_str_mv | AT bumsooahn diaphragmatrophyandcontractiledysfunctioninamurinemodelofpulmonaryhypertension AT hyacinthmempinado diaphragmatrophyandcontractiledysfunctioninamurinemodelofpulmonaryhypertension AT monsouralrajhi diaphragmatrophyandcontractiledysfunctioninamurinemodelofpulmonaryhypertension AT andrewrjudge diaphragmatrophyandcontractiledysfunctioninamurinemodelofpulmonaryhypertension AT leonardofferreira diaphragmatrophyandcontractiledysfunctioninamurinemodelofpulmonaryhypertension |