Abstract |
Given the hypothesis that inflammation plays a critical role in the progression of cardiovascular diseases, the aim of the present study was to identify new diagnostic and prognostic biomarkers of myocardial proteins involved in early-phase cardiac impairment, using proteomics analysis. Using the two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) combined with MALDI-TOF/TOF tandem mass spectrometry, we compared differences in the expression of proteins in the whole left ventricles between control hamsters, dilated cardiomyopathic hamsters (TO-2), and hypertrophy cardiomyopathic hamsters (Bio14.6) at 6 weeks of age (n = 6, each group). Proteomic analysis identified 10 protein spots with significant alterations, with 7 up-regulated and 3 down-regulated proteins in the left ventricles of both TO-2 and Bio 14.6 hamsters, compared with control hamsters. Of the total alterations, peroxiredoxin 2 (PRDX2) showed significant upregulation in the left ventricles of TO-2 and Bio 14.6 hamsters. Our data suggest that PRDX2, a redox regulating molecule, is involved in early-phase left ventricular impairment in hamsters with cardiomyopathy.
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Authors | Kentaro Kuzuya, Sahoko Ichihara, Yuka Suzuki, Chisa Inoue, Gaku Ichihara, Syota Kurimoto, Shinji Oikawa |
Journal | PloS one
(PLoS One)
Vol. 13
Issue 2
Pg. e0192624
( 2018)
ISSN: 1932-6203 [Electronic] United States |
PMID | 29438398
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Animals
- Body Weight
- Cardiomyopathies
(metabolism, physiopathology)
- Cricetinae
- Electrophoresis, Gel, Two-Dimensional
- Heart Ventricles
(metabolism, physiopathology)
- Male
- Mesocricetus
- Peroxiredoxins
(metabolism)
- Proteomics
- Reverse Transcriptase Polymerase Chain Reaction
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