Cardioprotective activity of placental growth factor combined with oral supplementation of L-arginine in a rat model of acute myocardial infarction
Liyun Luo,1,* Bairong Chen,1,* Yin Huang,1 Zibin Liang,2 Songbiao Li,1 Yuelan Yin,1 Jian Chen,1 Wei Wu1 1Department of Cardiology, 2Department of Oncological Radiotherapy, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, People’s Republic of China*These authors c...
Ausführliche Beschreibung
Autor*in: |
Luo L [verfasserIn] Chen B [verfasserIn] Huang Y [verfasserIn] Liang Z [verfasserIn] Li S [verfasserIn] Yin Y [verfasserIn] Chen J [verfasserIn] Wu W [verfasserIn] |
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Englisch |
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2016 |
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In: Drug Design, Development and Therapy - Dove Medical Press, 2008, (2016), Seite 3483-3492 |
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year:2016 ; pages:3483-3492 |
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DOAJ038364646 |
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520 | |a Liyun Luo,1,* Bairong Chen,1,* Yin Huang,1 Zibin Liang,2 Songbiao Li,1 Yuelan Yin,1 Jian Chen,1 Wei Wu1 1Department of Cardiology, 2Department of Oncological Radiotherapy, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, People’s Republic of China*These authors contributed equally to this workObjective: Exogenous administration of placental growth factor (PlGF) stimulates angiogenesis and improves ventricular remodeling after acute myocardial infarction (AMI), and supplementation with L-arginine ameliorates endothelial function. The objective of the present study was to compare the cardioprotective effects of combination therapy of PlGF and L-arginine with those of direct administration of PlGF alone in a rat model of AMI.Materials and methods: Fifty male Sprague Dawley rats were randomly divided into five groups: sham group, normal saline group, L-arginine group, PlGF group, and combination group (PlGF + L-arginine). An AMI rat model was established by ligation of the left anterior descending of coronary arteries. After 4 weeks of postligation treatment, cardiac function, scar area, angiogenesis and arteriogenesis, myocardial endothelial nitric oxide synthase (eNOS) and collagen I protein content, and plasma concentration of brain natriuretic peptide (BNP) were studied. Echocardiography, Masson’s staining, immunohistochemical analyses, Western blot, and enzyme-linked immunosorbent assay were performed.Results: Left ventricular ejection fraction (LVEF), left ventricular fraction shortening (LVFS), and capillary and arteriole densities were higher in the PlGF group than in the normal saline group (P<0.01). Scar area, collagen I protein content, and plasma concentration of BNP were decreased in the PlGF group (P<0.01). Myocardial eNOS protein level was elevated in the L-arginine group and PlGF + L-arginine group (P<0.01). Compared with the PlGF group, LVEF, LVFS, myocardial eNOS, and capillary and arteriole densities were higher in the combination group (P<0.01). Scar area, content of collagen I protein, and plasma concentration of BNP were reduced in the combination group (P<0.01).Conclusion: Exogenous administration of PlGF stimulates angiogenesis and improves cardiac function. L-arginine increases the expression of the eNOS protein. PlGF and L-arginine have a more pronounced, synergistic protective effect on myocardial protection compared with that of exogenous PlGF therapy alone. Keywords: placental growth factor, L-arginine, acute myocardial infarction, angiogenesis | ||
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(DE-627)DOAJ038364646 (DE-599)DOAJ5be31c31cdea4aceb374cb58a641a31c DE-627 ger DE-627 rakwb eng RM1-950 Luo L verfasserin aut Cardioprotective activity of placental growth factor combined with oral supplementation of L-arginine in a rat model of acute myocardial infarction 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Liyun Luo,1,* Bairong Chen,1,* Yin Huang,1 Zibin Liang,2 Songbiao Li,1 Yuelan Yin,1 Jian Chen,1 Wei Wu1 1Department of Cardiology, 2Department of Oncological Radiotherapy, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, People’s Republic of China*These authors contributed equally to this workObjective: Exogenous administration of placental growth factor (PlGF) stimulates angiogenesis and improves ventricular remodeling after acute myocardial infarction (AMI), and supplementation with L-arginine ameliorates endothelial function. The objective of the present study was to compare the cardioprotective effects of combination therapy of PlGF and L-arginine with those of direct administration of PlGF alone in a rat model of AMI.Materials and methods: Fifty male Sprague Dawley rats were randomly divided into five groups: sham group, normal saline group, L-arginine group, PlGF group, and combination group (PlGF + L-arginine). An AMI rat model was established by ligation of the left anterior descending of coronary arteries. After 4 weeks of postligation treatment, cardiac function, scar area, angiogenesis and arteriogenesis, myocardial endothelial nitric oxide synthase (eNOS) and collagen I protein content, and plasma concentration of brain natriuretic peptide (BNP) were studied. Echocardiography, Masson’s staining, immunohistochemical analyses, Western blot, and enzyme-linked immunosorbent assay were performed.Results: Left ventricular ejection fraction (LVEF), left ventricular fraction shortening (LVFS), and capillary and arteriole densities were higher in the PlGF group than in the normal saline group (P<0.01). Scar area, collagen I protein content, and plasma concentration of BNP were decreased in the PlGF group (P<0.01). Myocardial eNOS protein level was elevated in the L-arginine group and PlGF + L-arginine group (P<0.01). Compared with the PlGF group, LVEF, LVFS, myocardial eNOS, and capillary and arteriole densities were higher in the combination group (P<0.01). Scar area, content of collagen I protein, and plasma concentration of BNP were reduced in the combination group (P<0.01).Conclusion: Exogenous administration of PlGF stimulates angiogenesis and improves cardiac function. L-arginine increases the expression of the eNOS protein. PlGF and L-arginine have a more pronounced, synergistic protective effect on myocardial protection compared with that of exogenous PlGF therapy alone. Keywords: placental growth factor, L-arginine, acute myocardial infarction, angiogenesis placental growth factor L-arginine acute myocardial infarction angiogenesis Therapeutics. Pharmacology Chen B verfasserin aut Huang Y verfasserin aut Liang Z verfasserin aut Li S verfasserin aut Yin Y verfasserin aut Chen J verfasserin aut Wu W verfasserin aut In Drug Design, Development and Therapy Dove Medical Press, 2008 (2016), Seite 3483-3492 (DE-627)578533138 (DE-600)2451346-5 11778881 nnns year:2016 pages:3483-3492 https://doaj.org/article/5be31c31cdea4aceb374cb58a641a31c kostenfrei https://www.dovepress.com/cardioprotective-activity-of-placental-growth-factor-combined-with-ora-peer-reviewed-article-DDDT kostenfrei https://doaj.org/toc/1177-8881 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2016 3483-3492 |
spelling |
(DE-627)DOAJ038364646 (DE-599)DOAJ5be31c31cdea4aceb374cb58a641a31c DE-627 ger DE-627 rakwb eng RM1-950 Luo L verfasserin aut Cardioprotective activity of placental growth factor combined with oral supplementation of L-arginine in a rat model of acute myocardial infarction 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Liyun Luo,1,* Bairong Chen,1,* Yin Huang,1 Zibin Liang,2 Songbiao Li,1 Yuelan Yin,1 Jian Chen,1 Wei Wu1 1Department of Cardiology, 2Department of Oncological Radiotherapy, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, People’s Republic of China*These authors contributed equally to this workObjective: Exogenous administration of placental growth factor (PlGF) stimulates angiogenesis and improves ventricular remodeling after acute myocardial infarction (AMI), and supplementation with L-arginine ameliorates endothelial function. The objective of the present study was to compare the cardioprotective effects of combination therapy of PlGF and L-arginine with those of direct administration of PlGF alone in a rat model of AMI.Materials and methods: Fifty male Sprague Dawley rats were randomly divided into five groups: sham group, normal saline group, L-arginine group, PlGF group, and combination group (PlGF + L-arginine). An AMI rat model was established by ligation of the left anterior descending of coronary arteries. After 4 weeks of postligation treatment, cardiac function, scar area, angiogenesis and arteriogenesis, myocardial endothelial nitric oxide synthase (eNOS) and collagen I protein content, and plasma concentration of brain natriuretic peptide (BNP) were studied. Echocardiography, Masson’s staining, immunohistochemical analyses, Western blot, and enzyme-linked immunosorbent assay were performed.Results: Left ventricular ejection fraction (LVEF), left ventricular fraction shortening (LVFS), and capillary and arteriole densities were higher in the PlGF group than in the normal saline group (P<0.01). Scar area, collagen I protein content, and plasma concentration of BNP were decreased in the PlGF group (P<0.01). Myocardial eNOS protein level was elevated in the L-arginine group and PlGF + L-arginine group (P<0.01). Compared with the PlGF group, LVEF, LVFS, myocardial eNOS, and capillary and arteriole densities were higher in the combination group (P<0.01). Scar area, content of collagen I protein, and plasma concentration of BNP were reduced in the combination group (P<0.01).Conclusion: Exogenous administration of PlGF stimulates angiogenesis and improves cardiac function. L-arginine increases the expression of the eNOS protein. PlGF and L-arginine have a more pronounced, synergistic protective effect on myocardial protection compared with that of exogenous PlGF therapy alone. Keywords: placental growth factor, L-arginine, acute myocardial infarction, angiogenesis placental growth factor L-arginine acute myocardial infarction angiogenesis Therapeutics. Pharmacology Chen B verfasserin aut Huang Y verfasserin aut Liang Z verfasserin aut Li S verfasserin aut Yin Y verfasserin aut Chen J verfasserin aut Wu W verfasserin aut In Drug Design, Development and Therapy Dove Medical Press, 2008 (2016), Seite 3483-3492 (DE-627)578533138 (DE-600)2451346-5 11778881 nnns year:2016 pages:3483-3492 https://doaj.org/article/5be31c31cdea4aceb374cb58a641a31c kostenfrei https://www.dovepress.com/cardioprotective-activity-of-placental-growth-factor-combined-with-ora-peer-reviewed-article-DDDT kostenfrei https://doaj.org/toc/1177-8881 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2016 3483-3492 |
allfields_unstemmed |
(DE-627)DOAJ038364646 (DE-599)DOAJ5be31c31cdea4aceb374cb58a641a31c DE-627 ger DE-627 rakwb eng RM1-950 Luo L verfasserin aut Cardioprotective activity of placental growth factor combined with oral supplementation of L-arginine in a rat model of acute myocardial infarction 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Liyun Luo,1,* Bairong Chen,1,* Yin Huang,1 Zibin Liang,2 Songbiao Li,1 Yuelan Yin,1 Jian Chen,1 Wei Wu1 1Department of Cardiology, 2Department of Oncological Radiotherapy, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, People’s Republic of China*These authors contributed equally to this workObjective: Exogenous administration of placental growth factor (PlGF) stimulates angiogenesis and improves ventricular remodeling after acute myocardial infarction (AMI), and supplementation with L-arginine ameliorates endothelial function. The objective of the present study was to compare the cardioprotective effects of combination therapy of PlGF and L-arginine with those of direct administration of PlGF alone in a rat model of AMI.Materials and methods: Fifty male Sprague Dawley rats were randomly divided into five groups: sham group, normal saline group, L-arginine group, PlGF group, and combination group (PlGF + L-arginine). An AMI rat model was established by ligation of the left anterior descending of coronary arteries. After 4 weeks of postligation treatment, cardiac function, scar area, angiogenesis and arteriogenesis, myocardial endothelial nitric oxide synthase (eNOS) and collagen I protein content, and plasma concentration of brain natriuretic peptide (BNP) were studied. Echocardiography, Masson’s staining, immunohistochemical analyses, Western blot, and enzyme-linked immunosorbent assay were performed.Results: Left ventricular ejection fraction (LVEF), left ventricular fraction shortening (LVFS), and capillary and arteriole densities were higher in the PlGF group than in the normal saline group (P<0.01). Scar area, collagen I protein content, and plasma concentration of BNP were decreased in the PlGF group (P<0.01). Myocardial eNOS protein level was elevated in the L-arginine group and PlGF + L-arginine group (P<0.01). Compared with the PlGF group, LVEF, LVFS, myocardial eNOS, and capillary and arteriole densities were higher in the combination group (P<0.01). Scar area, content of collagen I protein, and plasma concentration of BNP were reduced in the combination group (P<0.01).Conclusion: Exogenous administration of PlGF stimulates angiogenesis and improves cardiac function. L-arginine increases the expression of the eNOS protein. PlGF and L-arginine have a more pronounced, synergistic protective effect on myocardial protection compared with that of exogenous PlGF therapy alone. Keywords: placental growth factor, L-arginine, acute myocardial infarction, angiogenesis placental growth factor L-arginine acute myocardial infarction angiogenesis Therapeutics. Pharmacology Chen B verfasserin aut Huang Y verfasserin aut Liang Z verfasserin aut Li S verfasserin aut Yin Y verfasserin aut Chen J verfasserin aut Wu W verfasserin aut In Drug Design, Development and Therapy Dove Medical Press, 2008 (2016), Seite 3483-3492 (DE-627)578533138 (DE-600)2451346-5 11778881 nnns year:2016 pages:3483-3492 https://doaj.org/article/5be31c31cdea4aceb374cb58a641a31c kostenfrei https://www.dovepress.com/cardioprotective-activity-of-placental-growth-factor-combined-with-ora-peer-reviewed-article-DDDT kostenfrei https://doaj.org/toc/1177-8881 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2016 3483-3492 |
allfieldsGer |
(DE-627)DOAJ038364646 (DE-599)DOAJ5be31c31cdea4aceb374cb58a641a31c DE-627 ger DE-627 rakwb eng RM1-950 Luo L verfasserin aut Cardioprotective activity of placental growth factor combined with oral supplementation of L-arginine in a rat model of acute myocardial infarction 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Liyun Luo,1,* Bairong Chen,1,* Yin Huang,1 Zibin Liang,2 Songbiao Li,1 Yuelan Yin,1 Jian Chen,1 Wei Wu1 1Department of Cardiology, 2Department of Oncological Radiotherapy, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, People’s Republic of China*These authors contributed equally to this workObjective: Exogenous administration of placental growth factor (PlGF) stimulates angiogenesis and improves ventricular remodeling after acute myocardial infarction (AMI), and supplementation with L-arginine ameliorates endothelial function. The objective of the present study was to compare the cardioprotective effects of combination therapy of PlGF and L-arginine with those of direct administration of PlGF alone in a rat model of AMI.Materials and methods: Fifty male Sprague Dawley rats were randomly divided into five groups: sham group, normal saline group, L-arginine group, PlGF group, and combination group (PlGF + L-arginine). An AMI rat model was established by ligation of the left anterior descending of coronary arteries. After 4 weeks of postligation treatment, cardiac function, scar area, angiogenesis and arteriogenesis, myocardial endothelial nitric oxide synthase (eNOS) and collagen I protein content, and plasma concentration of brain natriuretic peptide (BNP) were studied. Echocardiography, Masson’s staining, immunohistochemical analyses, Western blot, and enzyme-linked immunosorbent assay were performed.Results: Left ventricular ejection fraction (LVEF), left ventricular fraction shortening (LVFS), and capillary and arteriole densities were higher in the PlGF group than in the normal saline group (P<0.01). Scar area, collagen I protein content, and plasma concentration of BNP were decreased in the PlGF group (P<0.01). Myocardial eNOS protein level was elevated in the L-arginine group and PlGF + L-arginine group (P<0.01). Compared with the PlGF group, LVEF, LVFS, myocardial eNOS, and capillary and arteriole densities were higher in the combination group (P<0.01). Scar area, content of collagen I protein, and plasma concentration of BNP were reduced in the combination group (P<0.01).Conclusion: Exogenous administration of PlGF stimulates angiogenesis and improves cardiac function. L-arginine increases the expression of the eNOS protein. PlGF and L-arginine have a more pronounced, synergistic protective effect on myocardial protection compared with that of exogenous PlGF therapy alone. Keywords: placental growth factor, L-arginine, acute myocardial infarction, angiogenesis placental growth factor L-arginine acute myocardial infarction angiogenesis Therapeutics. Pharmacology Chen B verfasserin aut Huang Y verfasserin aut Liang Z verfasserin aut Li S verfasserin aut Yin Y verfasserin aut Chen J verfasserin aut Wu W verfasserin aut In Drug Design, Development and Therapy Dove Medical Press, 2008 (2016), Seite 3483-3492 (DE-627)578533138 (DE-600)2451346-5 11778881 nnns year:2016 pages:3483-3492 https://doaj.org/article/5be31c31cdea4aceb374cb58a641a31c kostenfrei https://www.dovepress.com/cardioprotective-activity-of-placental-growth-factor-combined-with-ora-peer-reviewed-article-DDDT kostenfrei https://doaj.org/toc/1177-8881 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2016 3483-3492 |
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(DE-627)DOAJ038364646 (DE-599)DOAJ5be31c31cdea4aceb374cb58a641a31c DE-627 ger DE-627 rakwb eng RM1-950 Luo L verfasserin aut Cardioprotective activity of placental growth factor combined with oral supplementation of L-arginine in a rat model of acute myocardial infarction 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Liyun Luo,1,* Bairong Chen,1,* Yin Huang,1 Zibin Liang,2 Songbiao Li,1 Yuelan Yin,1 Jian Chen,1 Wei Wu1 1Department of Cardiology, 2Department of Oncological Radiotherapy, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, People’s Republic of China*These authors contributed equally to this workObjective: Exogenous administration of placental growth factor (PlGF) stimulates angiogenesis and improves ventricular remodeling after acute myocardial infarction (AMI), and supplementation with L-arginine ameliorates endothelial function. The objective of the present study was to compare the cardioprotective effects of combination therapy of PlGF and L-arginine with those of direct administration of PlGF alone in a rat model of AMI.Materials and methods: Fifty male Sprague Dawley rats were randomly divided into five groups: sham group, normal saline group, L-arginine group, PlGF group, and combination group (PlGF + L-arginine). An AMI rat model was established by ligation of the left anterior descending of coronary arteries. After 4 weeks of postligation treatment, cardiac function, scar area, angiogenesis and arteriogenesis, myocardial endothelial nitric oxide synthase (eNOS) and collagen I protein content, and plasma concentration of brain natriuretic peptide (BNP) were studied. Echocardiography, Masson’s staining, immunohistochemical analyses, Western blot, and enzyme-linked immunosorbent assay were performed.Results: Left ventricular ejection fraction (LVEF), left ventricular fraction shortening (LVFS), and capillary and arteriole densities were higher in the PlGF group than in the normal saline group (P<0.01). Scar area, collagen I protein content, and plasma concentration of BNP were decreased in the PlGF group (P<0.01). Myocardial eNOS protein level was elevated in the L-arginine group and PlGF + L-arginine group (P<0.01). Compared with the PlGF group, LVEF, LVFS, myocardial eNOS, and capillary and arteriole densities were higher in the combination group (P<0.01). Scar area, content of collagen I protein, and plasma concentration of BNP were reduced in the combination group (P<0.01).Conclusion: Exogenous administration of PlGF stimulates angiogenesis and improves cardiac function. L-arginine increases the expression of the eNOS protein. PlGF and L-arginine have a more pronounced, synergistic protective effect on myocardial protection compared with that of exogenous PlGF therapy alone. Keywords: placental growth factor, L-arginine, acute myocardial infarction, angiogenesis placental growth factor L-arginine acute myocardial infarction angiogenesis Therapeutics. Pharmacology Chen B verfasserin aut Huang Y verfasserin aut Liang Z verfasserin aut Li S verfasserin aut Yin Y verfasserin aut Chen J verfasserin aut Wu W verfasserin aut In Drug Design, Development and Therapy Dove Medical Press, 2008 (2016), Seite 3483-3492 (DE-627)578533138 (DE-600)2451346-5 11778881 nnns year:2016 pages:3483-3492 https://doaj.org/article/5be31c31cdea4aceb374cb58a641a31c kostenfrei https://www.dovepress.com/cardioprotective-activity-of-placental-growth-factor-combined-with-ora-peer-reviewed-article-DDDT kostenfrei https://doaj.org/toc/1177-8881 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2016 3483-3492 |
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Cardioprotective activity of placental growth factor combined with oral supplementation of L-arginine in a rat model of acute myocardial infarction |
abstract |
Liyun Luo,1,* Bairong Chen,1,* Yin Huang,1 Zibin Liang,2 Songbiao Li,1 Yuelan Yin,1 Jian Chen,1 Wei Wu1 1Department of Cardiology, 2Department of Oncological Radiotherapy, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, People’s Republic of China*These authors contributed equally to this workObjective: Exogenous administration of placental growth factor (PlGF) stimulates angiogenesis and improves ventricular remodeling after acute myocardial infarction (AMI), and supplementation with L-arginine ameliorates endothelial function. The objective of the present study was to compare the cardioprotective effects of combination therapy of PlGF and L-arginine with those of direct administration of PlGF alone in a rat model of AMI.Materials and methods: Fifty male Sprague Dawley rats were randomly divided into five groups: sham group, normal saline group, L-arginine group, PlGF group, and combination group (PlGF + L-arginine). An AMI rat model was established by ligation of the left anterior descending of coronary arteries. After 4 weeks of postligation treatment, cardiac function, scar area, angiogenesis and arteriogenesis, myocardial endothelial nitric oxide synthase (eNOS) and collagen I protein content, and plasma concentration of brain natriuretic peptide (BNP) were studied. Echocardiography, Masson’s staining, immunohistochemical analyses, Western blot, and enzyme-linked immunosorbent assay were performed.Results: Left ventricular ejection fraction (LVEF), left ventricular fraction shortening (LVFS), and capillary and arteriole densities were higher in the PlGF group than in the normal saline group (P<0.01). Scar area, collagen I protein content, and plasma concentration of BNP were decreased in the PlGF group (P<0.01). Myocardial eNOS protein level was elevated in the L-arginine group and PlGF + L-arginine group (P<0.01). Compared with the PlGF group, LVEF, LVFS, myocardial eNOS, and capillary and arteriole densities were higher in the combination group (P<0.01). Scar area, content of collagen I protein, and plasma concentration of BNP were reduced in the combination group (P<0.01).Conclusion: Exogenous administration of PlGF stimulates angiogenesis and improves cardiac function. L-arginine increases the expression of the eNOS protein. PlGF and L-arginine have a more pronounced, synergistic protective effect on myocardial protection compared with that of exogenous PlGF therapy alone. Keywords: placental growth factor, L-arginine, acute myocardial infarction, angiogenesis |
abstractGer |
Liyun Luo,1,* Bairong Chen,1,* Yin Huang,1 Zibin Liang,2 Songbiao Li,1 Yuelan Yin,1 Jian Chen,1 Wei Wu1 1Department of Cardiology, 2Department of Oncological Radiotherapy, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, People’s Republic of China*These authors contributed equally to this workObjective: Exogenous administration of placental growth factor (PlGF) stimulates angiogenesis and improves ventricular remodeling after acute myocardial infarction (AMI), and supplementation with L-arginine ameliorates endothelial function. The objective of the present study was to compare the cardioprotective effects of combination therapy of PlGF and L-arginine with those of direct administration of PlGF alone in a rat model of AMI.Materials and methods: Fifty male Sprague Dawley rats were randomly divided into five groups: sham group, normal saline group, L-arginine group, PlGF group, and combination group (PlGF + L-arginine). An AMI rat model was established by ligation of the left anterior descending of coronary arteries. After 4 weeks of postligation treatment, cardiac function, scar area, angiogenesis and arteriogenesis, myocardial endothelial nitric oxide synthase (eNOS) and collagen I protein content, and plasma concentration of brain natriuretic peptide (BNP) were studied. Echocardiography, Masson’s staining, immunohistochemical analyses, Western blot, and enzyme-linked immunosorbent assay were performed.Results: Left ventricular ejection fraction (LVEF), left ventricular fraction shortening (LVFS), and capillary and arteriole densities were higher in the PlGF group than in the normal saline group (P<0.01). Scar area, collagen I protein content, and plasma concentration of BNP were decreased in the PlGF group (P<0.01). Myocardial eNOS protein level was elevated in the L-arginine group and PlGF + L-arginine group (P<0.01). Compared with the PlGF group, LVEF, LVFS, myocardial eNOS, and capillary and arteriole densities were higher in the combination group (P<0.01). Scar area, content of collagen I protein, and plasma concentration of BNP were reduced in the combination group (P<0.01).Conclusion: Exogenous administration of PlGF stimulates angiogenesis and improves cardiac function. L-arginine increases the expression of the eNOS protein. PlGF and L-arginine have a more pronounced, synergistic protective effect on myocardial protection compared with that of exogenous PlGF therapy alone. Keywords: placental growth factor, L-arginine, acute myocardial infarction, angiogenesis |
abstract_unstemmed |
Liyun Luo,1,* Bairong Chen,1,* Yin Huang,1 Zibin Liang,2 Songbiao Li,1 Yuelan Yin,1 Jian Chen,1 Wei Wu1 1Department of Cardiology, 2Department of Oncological Radiotherapy, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, People’s Republic of China*These authors contributed equally to this workObjective: Exogenous administration of placental growth factor (PlGF) stimulates angiogenesis and improves ventricular remodeling after acute myocardial infarction (AMI), and supplementation with L-arginine ameliorates endothelial function. The objective of the present study was to compare the cardioprotective effects of combination therapy of PlGF and L-arginine with those of direct administration of PlGF alone in a rat model of AMI.Materials and methods: Fifty male Sprague Dawley rats were randomly divided into five groups: sham group, normal saline group, L-arginine group, PlGF group, and combination group (PlGF + L-arginine). An AMI rat model was established by ligation of the left anterior descending of coronary arteries. After 4 weeks of postligation treatment, cardiac function, scar area, angiogenesis and arteriogenesis, myocardial endothelial nitric oxide synthase (eNOS) and collagen I protein content, and plasma concentration of brain natriuretic peptide (BNP) were studied. Echocardiography, Masson’s staining, immunohistochemical analyses, Western blot, and enzyme-linked immunosorbent assay were performed.Results: Left ventricular ejection fraction (LVEF), left ventricular fraction shortening (LVFS), and capillary and arteriole densities were higher in the PlGF group than in the normal saline group (P<0.01). Scar area, collagen I protein content, and plasma concentration of BNP were decreased in the PlGF group (P<0.01). Myocardial eNOS protein level was elevated in the L-arginine group and PlGF + L-arginine group (P<0.01). Compared with the PlGF group, LVEF, LVFS, myocardial eNOS, and capillary and arteriole densities were higher in the combination group (P<0.01). Scar area, content of collagen I protein, and plasma concentration of BNP were reduced in the combination group (P<0.01).Conclusion: Exogenous administration of PlGF stimulates angiogenesis and improves cardiac function. L-arginine increases the expression of the eNOS protein. PlGF and L-arginine have a more pronounced, synergistic protective effect on myocardial protection compared with that of exogenous PlGF therapy alone. Keywords: placental growth factor, L-arginine, acute myocardial infarction, angiogenesis |
collection_details |
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title_short |
Cardioprotective activity of placental growth factor combined with oral supplementation of L-arginine in a rat model of acute myocardial infarction |
url |
https://doaj.org/article/5be31c31cdea4aceb374cb58a641a31c https://www.dovepress.com/cardioprotective-activity-of-placental-growth-factor-combined-with-ora-peer-reviewed-article-DDDT https://doaj.org/toc/1177-8881 |
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Chen B Huang Y Liang Z Li S Yin Y Chen J Wu W |
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The objective of the present study was to compare the cardioprotective effects of combination therapy of PlGF and L-arginine with those of direct administration of PlGF alone in a rat model of AMI.Materials and methods: Fifty male Sprague Dawley rats were randomly divided into five groups: sham group, normal saline group, L-arginine group, PlGF group, and combination group (PlGF + L-arginine). An AMI rat model was established by ligation of the left anterior descending of coronary arteries. After 4 weeks of postligation treatment, cardiac function, scar area, angiogenesis and arteriogenesis, myocardial endothelial nitric oxide synthase (eNOS) and collagen I protein content, and plasma concentration of brain natriuretic peptide (BNP) were studied. 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