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Tongxinluo protects against pressure overload-induced heart failure in mice involving VEGF/Akt/eNOS pathway activation

It has been demonstrated that Tongxinluo (TXL), a traditional Chinese medicine compound, improves ischemic heart disease in animal models via vascular endothelial growth factor (VEGF) and endothelial nitric oxide synthase (eNOS). The present study aimed to investigate whether TXL protects against pr...

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Published in:PloS one 2014-06, Vol.9 (6), p.e98047-e98047
Main Authors: Wang, Bo, Yang, Qing, Bai, Wen-wu, Xing, Yi-fan, Lu, Xiao-ting, Sun, Yuan-yuan, Zhao, Yu-xia
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Yang, Qing
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description It has been demonstrated that Tongxinluo (TXL), a traditional Chinese medicine compound, improves ischemic heart disease in animal models via vascular endothelial growth factor (VEGF) and endothelial nitric oxide synthase (eNOS). The present study aimed to investigate whether TXL protects against pressure overload-induced heart failure in mice and explore the possible mechanism of action. Transverse aortic constriction (TAC) surgery was performed in mice to induce heart failure. Cardiac function was evaluated by echocardiography. Myocardial pathology was detected using hematoxylin and eosin or Masson trichrome staining. We investigated cardiomyocyte ultrastructure using transmission electron microscopy. Angiogenesis and oxidative stress levels were determined using CD31 and 8-hydroxydeoxyguanosine immunostaining and malondialdehyde assay, respectively. Fetal gene expression was measured using real-time PCR. Protein expression of VEGF, phosphorylated (p)-VEGF receptor 2 (VEGFR2), p-phosphatidylinositol 3-kinase (PI3K), p-Akt, p-eNOS, heme oxygenase-1 (HO-1), and NADPH oxidase 4 (Nox4) were measured with western blotting. Twelve-week low- and high-dose TXL treatment following TAC improved cardiac systolic and diastolic function and ameliorated left ventricular hypertrophy, fibrosis, and myocardial ultrastructure derangement. Importantly, TXL increased myocardial capillary density significantly and attenuated oxidative stress injury in failing hearts. Moreover, TXL upregulated cardiac nitrite content and the protein expression of VEGF, p-VEGFR2, p-PI3K, p-Akt, p-eNOS, and HO-1, but decreased Nox4 expression in mouse heart following TAC. Our findings indicate that TXL protects against pressure overload-induced heart failure in mice. Activation of the VEGF/Akt/eNOS signaling pathway might be involved in TXL improvement of the failing heart.
doi_str_mv 10.1371/journal.pone.0098047
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The present study aimed to investigate whether TXL protects against pressure overload-induced heart failure in mice and explore the possible mechanism of action. Transverse aortic constriction (TAC) surgery was performed in mice to induce heart failure. Cardiac function was evaluated by echocardiography. Myocardial pathology was detected using hematoxylin and eosin or Masson trichrome staining. We investigated cardiomyocyte ultrastructure using transmission electron microscopy. Angiogenesis and oxidative stress levels were determined using CD31 and 8-hydroxydeoxyguanosine immunostaining and malondialdehyde assay, respectively. Fetal gene expression was measured using real-time PCR. Protein expression of VEGF, phosphorylated (p)-VEGF receptor 2 (VEGFR2), p-phosphatidylinositol 3-kinase (PI3K), p-Akt, p-eNOS, heme oxygenase-1 (HO-1), and NADPH oxidase 4 (Nox4) were measured with western blotting. 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Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials science collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Bo</au><au>Yang, Qing</au><au>Bai, Wen-wu</au><au>Xing, Yi-fan</au><au>Lu, Xiao-ting</au><au>Sun, Yuan-yuan</au><au>Zhao, Yu-xia</au><au>Zhou, Hua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tongxinluo protects against pressure overload-induced heart failure in mice involving VEGF/Akt/eNOS pathway activation</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2014-06-02</date><risdate>2014</risdate><volume>9</volume><issue>6</issue><spage>e98047</spage><epage>e98047</epage><pages>e98047-e98047</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>It has been demonstrated that Tongxinluo (TXL), a traditional Chinese medicine compound, improves ischemic heart disease in animal models via vascular endothelial growth factor (VEGF) and endothelial nitric oxide synthase (eNOS). The present study aimed to investigate whether TXL protects against pressure overload-induced heart failure in mice and explore the possible mechanism of action. Transverse aortic constriction (TAC) surgery was performed in mice to induce heart failure. Cardiac function was evaluated by echocardiography. Myocardial pathology was detected using hematoxylin and eosin or Masson trichrome staining. We investigated cardiomyocyte ultrastructure using transmission electron microscopy. Angiogenesis and oxidative stress levels were determined using CD31 and 8-hydroxydeoxyguanosine immunostaining and malondialdehyde assay, respectively. Fetal gene expression was measured using real-time PCR. Protein expression of VEGF, phosphorylated (p)-VEGF receptor 2 (VEGFR2), p-phosphatidylinositol 3-kinase (PI3K), p-Akt, p-eNOS, heme oxygenase-1 (HO-1), and NADPH oxidase 4 (Nox4) were measured with western blotting. Twelve-week low- and high-dose TXL treatment following TAC improved cardiac systolic and diastolic function and ameliorated left ventricular hypertrophy, fibrosis, and myocardial ultrastructure derangement. Importantly, TXL increased myocardial capillary density significantly and attenuated oxidative stress injury in failing hearts. Moreover, TXL upregulated cardiac nitrite content and the protein expression of VEGF, p-VEGFR2, p-PI3K, p-Akt, p-eNOS, and HO-1, but decreased Nox4 expression in mouse heart following TAC. Our findings indicate that TXL protects against pressure overload-induced heart failure in mice. Activation of the VEGF/Akt/eNOS signaling pathway might be involved in TXL improvement of the failing heart.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24887083</pmid><doi>10.1371/journal.pone.0098047</doi><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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subjects 1-Phosphatidylinositol 3-kinase
8-Hydroxydeoxyguanosine
Activation
AKT protein
Analysis
Angiogenesis
Animal diseases
Animal models
Animals
Aorta
Biology and Life Sciences
Capillaries - drug effects
Capillaries - pathology
Capillaries - physiopathology
Cardiomegaly - diagnostic imaging
Cardiomegaly - metabolism
Cardiomegaly - pathology
Cardiomegaly - physiopathology
Cardiomyocytes
Cardiotonic Agents - pharmacology
Cardiotonic Agents - therapeutic use
Cardiovascular diseases
Chinese medicine
Coronary artery disease
Deoxyguanosine - analogs & derivatives
Deoxyguanosine - metabolism
Drugs, Chinese Herbal - pharmacology
Drugs, Chinese Herbal - therapeutic use
Echocardiography
Electron microscopy
Fetuses
Fibrosis
Gene expression
Heart
Heart diseases
Heart failure
Heart Failure - diagnostic imaging
Heart Failure - drug therapy
Heart Failure - metabolism
Heart Failure - physiopathology
Heart Function Tests
Heme
Heme oxygenase (decyclizing)
Herbal medicine
Hypertrophy
Ischemia
Kinases
Male
Malondialdehyde
Medicine and Health Sciences
Mice
Mice, Inbred C57BL
Myocardium - pathology
Myocardium - ultrastructure
NAD(P)H oxidase
Nitric oxide
Nitric Oxide Synthase Type III - metabolism
Oxidases
Oxidative stress
Oxidative Stress - drug effects
Pressure
Proto-Oncogene Proteins c-akt - metabolism
Research and Analysis Methods
Rodents
Signal transduction
Signal Transduction - drug effects
Signaling
Surgery
Traditional Chinese medicine
Transmission electron microscopy
Ultrasonography
Ultrastructure
Vascular endothelial growth factor
Vascular Endothelial Growth Factor A - metabolism
Ventricle
Western blotting
title Tongxinluo protects against pressure overload-induced heart failure in mice involving VEGF/Akt/eNOS pathway activation
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