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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 |
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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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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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0098047</identifier><identifier>PMID: 24887083</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>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</subject><ispartof>PloS one, 2014-06, Vol.9 (6), p.e98047-e98047</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Wang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 Wang et al 2014 Wang et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-5559897343f3bea89bff2fbe31e1e9fe15a5e5c0f228de67172dca6171a398323</citedby><cites>FETCH-LOGICAL-c758t-5559897343f3bea89bff2fbe31e1e9fe15a5e5c0f228de67172dca6171a398323</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1531472614/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1531472614?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,25740,27911,27912,36999,37000,44577,53778,53780,74881</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24887083$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Zhou, Hua</contributor><creatorcontrib>Wang, Bo</creatorcontrib><creatorcontrib>Yang, Qing</creatorcontrib><creatorcontrib>Bai, Wen-wu</creatorcontrib><creatorcontrib>Xing, Yi-fan</creatorcontrib><creatorcontrib>Lu, Xiao-ting</creatorcontrib><creatorcontrib>Sun, Yuan-yuan</creatorcontrib><creatorcontrib>Zhao, Yu-xia</creatorcontrib><title>Tongxinluo protects against pressure overload-induced heart failure in mice involving VEGF/Akt/eNOS pathway activation</title><title>PloS one</title><addtitle>PLoS One</addtitle><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.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>8-Hydroxydeoxyguanosine</subject><subject>Activation</subject><subject>AKT protein</subject><subject>Analysis</subject><subject>Angiogenesis</subject><subject>Animal diseases</subject><subject>Animal models</subject><subject>Animals</subject><subject>Aorta</subject><subject>Biology and Life Sciences</subject><subject>Capillaries - drug effects</subject><subject>Capillaries - pathology</subject><subject>Capillaries - physiopathology</subject><subject>Cardiomegaly - diagnostic imaging</subject><subject>Cardiomegaly - metabolism</subject><subject>Cardiomegaly - pathology</subject><subject>Cardiomegaly - physiopathology</subject><subject>Cardiomyocytes</subject><subject>Cardiotonic Agents - pharmacology</subject><subject>Cardiotonic Agents - therapeutic use</subject><subject>Cardiovascular diseases</subject><subject>Chinese medicine</subject><subject>Coronary artery disease</subject><subject>Deoxyguanosine - analogs & derivatives</subject><subject>Deoxyguanosine - metabolism</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Drugs, Chinese Herbal - therapeutic use</subject><subject>Echocardiography</subject><subject>Electron microscopy</subject><subject>Fetuses</subject><subject>Fibrosis</subject><subject>Gene expression</subject><subject>Heart</subject><subject>Heart diseases</subject><subject>Heart failure</subject><subject>Heart Failure - diagnostic imaging</subject><subject>Heart Failure - drug therapy</subject><subject>Heart Failure - metabolism</subject><subject>Heart Failure - physiopathology</subject><subject>Heart Function Tests</subject><subject>Heme</subject><subject>Heme oxygenase (decyclizing)</subject><subject>Herbal medicine</subject><subject>Hypertrophy</subject><subject>Ischemia</subject><subject>Kinases</subject><subject>Male</subject><subject>Malondialdehyde</subject><subject>Medicine and Health Sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Myocardium - pathology</subject><subject>Myocardium - ultrastructure</subject><subject>NAD(P)H oxidase</subject><subject>Nitric oxide</subject><subject>Nitric Oxide Synthase Type III - metabolism</subject><subject>Oxidases</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Pressure</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Research and Analysis Methods</subject><subject>Rodents</subject><subject>Signal transduction</subject><subject>Signal Transduction - drug effects</subject><subject>Signaling</subject><subject>Surgery</subject><subject>Traditional Chinese medicine</subject><subject>Transmission electron microscopy</subject><subject>Ultrasonography</subject><subject>Ultrastructure</subject><subject>Vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><subject>Ventricle</subject><subject>Western blotting</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk1Fv0zAQxyMEYmPwDRBEQkLw0NaOkzh5QaqmbVSaqMTGXi3XOacurt3FTti-Pc6aTQ3aA_KDrfPv_uc730XRe4ymmFA829i2MVxPd9bAFKGyQCl9ER3jkiSTPEHk5cH5KHrj3AahjBR5_jo6StKioKggx1F3bU19p4xubbxrrAfhXcxrrozzwQDOtQ3EtoNGW15NlKlaAVW8Bt74WHKl-2tl4q0S_d5Z3SlTxzdnF-ez-W8_gx_Lq3jH_foPv4-58KrjXlnzNnoluXbwbthPol_nZ9en3yeXy4vF6fxyImhW-EmWZWVRUpISSVbAi3IlZSJXQDBgKCXgjGeQCSSTpKggp5gmleA5ppiTsiAJOYk-7nV32jo2lMwxnBGc0iTHaSAWe6KyfMN2jdry5p5ZrtiDwTY1C6kqoYFVWYJkSQWlAtJCiELwElerEBgqSGUVtL4N0drVFioBxjdcj0THN0atWW07lqIU5xkOAl8GgcbetuA82yonQGtuwLYP705SWuK8DOinf9DnsxuomocElJE2xBW9KJuHkJRSRPqw02eosCoI_xr6S6pgHzl8HTkExsOdr3nrHFtc_fx_dnkzZj8fsKHJtF87q9u-ZdwYTPegaKxzDcinImPE-vF4rAbrx4MN4xHcPhx-0JPT4zyQv8sTDMM</recordid><startdate>20140602</startdate><enddate>20140602</enddate><creator>Wang, Bo</creator><creator>Yang, Qing</creator><creator>Bai, Wen-wu</creator><creator>Xing, Yi-fan</creator><creator>Lu, Xiao-ting</creator><creator>Sun, Yuan-yuan</creator><creator>Zhao, Yu-xia</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140602</creationdate><title>Tongxinluo protects against pressure overload-induced heart failure in mice involving VEGF/Akt/eNOS pathway activation</title><author>Wang, Bo ; Yang, Qing ; Bai, Wen-wu ; Xing, Yi-fan ; Lu, Xiao-ting ; Sun, Yuan-yuan ; Zhao, Yu-xia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c758t-5559897343f3bea89bff2fbe31e1e9fe15a5e5c0f228de67172dca6171a398323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>8-Hydroxydeoxyguanosine</topic><topic>Activation</topic><topic>AKT protein</topic><topic>Analysis</topic><topic>Angiogenesis</topic><topic>Animal diseases</topic><topic>Animal models</topic><topic>Animals</topic><topic>Aorta</topic><topic>Biology and Life Sciences</topic><topic>Capillaries - drug effects</topic><topic>Capillaries - pathology</topic><topic>Capillaries - physiopathology</topic><topic>Cardiomegaly - diagnostic imaging</topic><topic>Cardiomegaly - metabolism</topic><topic>Cardiomegaly - pathology</topic><topic>Cardiomegaly - physiopathology</topic><topic>Cardiomyocytes</topic><topic>Cardiotonic Agents - pharmacology</topic><topic>Cardiotonic Agents - therapeutic use</topic><topic>Cardiovascular diseases</topic><topic>Chinese medicine</topic><topic>Coronary artery disease</topic><topic>Deoxyguanosine - analogs & derivatives</topic><topic>Deoxyguanosine - metabolism</topic><topic>Drugs, Chinese Herbal - pharmacology</topic><topic>Drugs, Chinese Herbal - therapeutic use</topic><topic>Echocardiography</topic><topic>Electron microscopy</topic><topic>Fetuses</topic><topic>Fibrosis</topic><topic>Gene expression</topic><topic>Heart</topic><topic>Heart diseases</topic><topic>Heart failure</topic><topic>Heart Failure - diagnostic imaging</topic><topic>Heart Failure - drug therapy</topic><topic>Heart Failure - metabolism</topic><topic>Heart Failure - physiopathology</topic><topic>Heart Function Tests</topic><topic>Heme</topic><topic>Heme oxygenase (decyclizing)</topic><topic>Herbal medicine</topic><topic>Hypertrophy</topic><topic>Ischemia</topic><topic>Kinases</topic><topic>Male</topic><topic>Malondialdehyde</topic><topic>Medicine and Health Sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Myocardium - pathology</topic><topic>Myocardium - ultrastructure</topic><topic>NAD(P)H oxidase</topic><topic>Nitric oxide</topic><topic>Nitric Oxide Synthase Type III - metabolism</topic><topic>Oxidases</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Pressure</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>Research and Analysis Methods</topic><topic>Rodents</topic><topic>Signal transduction</topic><topic>Signal Transduction - drug effects</topic><topic>Signaling</topic><topic>Surgery</topic><topic>Traditional Chinese medicine</topic><topic>Transmission electron microscopy</topic><topic>Ultrasonography</topic><topic>Ultrastructure</topic><topic>Vascular endothelial growth factor</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><topic>Ventricle</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Bo</creatorcontrib><creatorcontrib>Yang, Qing</creatorcontrib><creatorcontrib>Bai, Wen-wu</creatorcontrib><creatorcontrib>Xing, Yi-fan</creatorcontrib><creatorcontrib>Lu, Xiao-ting</creatorcontrib><creatorcontrib>Sun, Yuan-yuan</creatorcontrib><creatorcontrib>Zhao, Yu-xia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Opposing Viewpoints In Context</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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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> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2014-06, Vol.9 (6), p.e98047-e98047 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1531472614 |
source | Open Access: PubMed Central; Publicly Available Content Database |
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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