Proteomic and metabolomic characterization of cardiac tissue in acute myocardial ischemia injury rats.

The pathological process and mechanism of myocardial ischemia (MI) is very complicated, and remains unclear. An integrated proteomic-metabolomics analysis was applied to comprehensively understand the pathological changes and mechanism of MI. Male Sprague-Dawley rats were randomly divided into a moc...

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Main Authors: Hua Bai, Ke Sun, Jia-Hong Wu, Ze-Hao Zhong, Sen-Lei Xu, Hong-Ru Zhang, Yi-Huang Gu, Sheng-Feng Lu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0231797
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author Hua Bai
Ke Sun
Jia-Hong Wu
Ze-Hao Zhong
Sen-Lei Xu
Hong-Ru Zhang
Yi-Huang Gu
Sheng-Feng Lu
author_facet Hua Bai
Ke Sun
Jia-Hong Wu
Ze-Hao Zhong
Sen-Lei Xu
Hong-Ru Zhang
Yi-Huang Gu
Sheng-Feng Lu
author_sort Hua Bai
collection DOAJ
description The pathological process and mechanism of myocardial ischemia (MI) is very complicated, and remains unclear. An integrated proteomic-metabolomics analysis was applied to comprehensively understand the pathological changes and mechanism of MI. Male Sprague-Dawley rats were randomly divided into a mock surgery (MS) group and an MI group. The MI model was made by ligating the left anterior descending coronary artery, twenty-four hours after which, echocardiography was employed to assess left ventricular (LV) function variables. Blood samples and left ventricular tissues were collected for ELISA, metabolomics and proteomics analysis. The results showed that LV function, including ejection fraction (EF) and fractional shortening (FS), was significantly reduced and the level of cTnT in the serum increased after MI. iTRAQ proteomics showed that a total of 169 proteins were altered including 52 and 117 proteins with increased and decreased expression, respectively, which were mainly involved in the following activities: complement and coagulation cascades, tight junction, regulation of actin cytoskeleton, MAPK signaling pathway, endocytosis, NOD-like receptor signaling pathway, as well as phagosome coupled with vitamin digestion and absorption. Altered metabolomic profiling of this transition was mostly enriched in pathways including ABC transporters, glycerophospholipid metabolism, protein digestion and absorption and aminoacyl-tRNA biosynthesis. The integrated metabolomics and proteomics analysis indicated that myocardial injury after MI is closely related to several metabolic pathways, especially energy metabolism, amino acid metabolism, vascular smooth muscle contraction, gap junction and neuroactive ligand-receptor interaction. These findings may contribute to understanding the mechanism of MI and have implication for new therapeutic targets.
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spelling doaj.art-8ff05f3d0e444709b9b0ab830669dd242022-12-21T22:35:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01155e023179710.1371/journal.pone.0231797Proteomic and metabolomic characterization of cardiac tissue in acute myocardial ischemia injury rats.Hua BaiKe SunJia-Hong WuZe-Hao ZhongSen-Lei XuHong-Ru ZhangYi-Huang GuSheng-Feng LuThe pathological process and mechanism of myocardial ischemia (MI) is very complicated, and remains unclear. An integrated proteomic-metabolomics analysis was applied to comprehensively understand the pathological changes and mechanism of MI. Male Sprague-Dawley rats were randomly divided into a mock surgery (MS) group and an MI group. The MI model was made by ligating the left anterior descending coronary artery, twenty-four hours after which, echocardiography was employed to assess left ventricular (LV) function variables. Blood samples and left ventricular tissues were collected for ELISA, metabolomics and proteomics analysis. The results showed that LV function, including ejection fraction (EF) and fractional shortening (FS), was significantly reduced and the level of cTnT in the serum increased after MI. iTRAQ proteomics showed that a total of 169 proteins were altered including 52 and 117 proteins with increased and decreased expression, respectively, which were mainly involved in the following activities: complement and coagulation cascades, tight junction, regulation of actin cytoskeleton, MAPK signaling pathway, endocytosis, NOD-like receptor signaling pathway, as well as phagosome coupled with vitamin digestion and absorption. Altered metabolomic profiling of this transition was mostly enriched in pathways including ABC transporters, glycerophospholipid metabolism, protein digestion and absorption and aminoacyl-tRNA biosynthesis. The integrated metabolomics and proteomics analysis indicated that myocardial injury after MI is closely related to several metabolic pathways, especially energy metabolism, amino acid metabolism, vascular smooth muscle contraction, gap junction and neuroactive ligand-receptor interaction. These findings may contribute to understanding the mechanism of MI and have implication for new therapeutic targets.https://doi.org/10.1371/journal.pone.0231797
spellingShingle Hua Bai
Ke Sun
Jia-Hong Wu
Ze-Hao Zhong
Sen-Lei Xu
Hong-Ru Zhang
Yi-Huang Gu
Sheng-Feng Lu
Proteomic and metabolomic characterization of cardiac tissue in acute myocardial ischemia injury rats.
PLoS ONE
title Proteomic and metabolomic characterization of cardiac tissue in acute myocardial ischemia injury rats.
title_full Proteomic and metabolomic characterization of cardiac tissue in acute myocardial ischemia injury rats.
title_fullStr Proteomic and metabolomic characterization of cardiac tissue in acute myocardial ischemia injury rats.
title_full_unstemmed Proteomic and metabolomic characterization of cardiac tissue in acute myocardial ischemia injury rats.
title_short Proteomic and metabolomic characterization of cardiac tissue in acute myocardial ischemia injury rats.
title_sort proteomic and metabolomic characterization of cardiac tissue in acute myocardial ischemia injury rats
url https://doi.org/10.1371/journal.pone.0231797
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