Myocardial Apelin Production is Reduced in Humans With Left Ventricular Systolic Dysfunction

Apelin is a novel endogenous peptide with inotropic and vasodilatory properties that is the ligand for the APJ receptor. Apelin and APJ are widely distributed in the vasculature of a number of organs and peripheral venous apelin is reduced in heart failure (HF). The location of apelin production in...

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Published inJournal of cardiac failure Vol. 16; no. 7; pp. 556 - 561
Main Authors Chandrasekaran, Badrinathan, Kalra, Paul R., Donovan, Jackie, Hooper, James, Clague, Jonathon R., McDonagh, Theresa A.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.07.2010
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Abstract Apelin is a novel endogenous peptide with inotropic and vasodilatory properties that is the ligand for the APJ receptor. Apelin and APJ are widely distributed in the vasculature of a number of organs and peripheral venous apelin is reduced in heart failure (HF). The location of apelin production in humans with and without HF was investigated. Plasma apelin and brain natriuretic peptide (BNP) concentrations in coronary sinus (CS), aorta (Ao), and renal vein (RV) of individuals with HF (n = 9) were compared to subjects with normal structural hearts (n = 8). In HF the concentration of CS apelin was reduced compared with controls (310 pg/mL [interquartile range 290-390] vs. 470 pg/mL [340-570], P < .035) but Ao apelin (330 pg/mL [275-375] vs. 340 pg/mL [230-455], P = .76) and RV apelin (290 pg/mL [280-360] vs. 370 pg/mL [273-410], P = .56) were unchanged. Plasma BNP was increased at all sampling sites in patients with HF as compared with controls. A step down from CS to Ao to RV in all subjects was observed. The step down in apelin from CS to Ao (470 pg/mL [310-595] vs. 320 pg/mL [225-482], P < .04) in control subjects was not apparent in patients with HF. These novel data show that apelin is produced in the human heart and that production is reduced in individuals with HF. In contrast to BNP, apelin production is not exclusive to the heart.
AbstractList Apelin is a novel endogenous peptide with inotropic and vasodilatory properties that is the ligand for the APJ receptor. Apelin and APJ are widely distributed in the vasculature of a number of organs and peripheral venous apelin is reduced in heart failure (HF). The location of apelin production in humans with and without HF was investigated. Plasma apelin and brain natriuretic peptide (BNP) concentrations in coronary sinus (CS), aorta (Ao), and renal vein (RV) of individuals with HF (n = 9) were compared to subjects with normal structural hearts (n = 8). In HF the concentration of CS apelin was reduced compared with controls (310 pg/mL [interquartile range 290-390] vs. 470 pg/mL [340-570], P < .035) but Ao apelin (330 pg/mL [275-375] vs. 340 pg/mL [230-455], P = .76) and RV apelin (290 pg/mL [280-360] vs. 370 pg/mL [273-410], P = .56) were unchanged. Plasma BNP was increased at all sampling sites in patients with HF as compared with controls. A step down from CS to Ao to RV in all subjects was observed. The step down in apelin from CS to Ao (470 pg/mL [310-595] vs. 320 pg/mL [225-482], P < .04) in control subjects was not apparent in patients with HF. These novel data show that apelin is produced in the human heart and that production is reduced in individuals with HF. In contrast to BNP, apelin production is not exclusive to the heart.
Apelin is a novel endogenous peptide with inotropic and vasodilatory properties that is the ligand for the APJ receptor. Apelin and APJ are widely distributed in the vasculature of a number of organs and peripheral venous apelin is reduced in heart failure (HF). The location of apelin production in humans with and without HF was investigated. Plasma apelin and brain natriuretic peptide (BNP) concentrations in coronary sinus (CS), aorta (Ao), and renal vein (RV) of individuals with HF (n = 9) were compared to subjects with normal structural hearts (n = 8). In HF the concentration of CS apelin was reduced compared with controls (310 pg/mL [interquartile range 290-390] vs. 470 pg/mL [340-570], P < .035) but Ao apelin (330 pg/mL [275-375] vs. 340 pg/mL [230-455], P = .76) and RV apelin (290 pg/mL [280-360] vs. 370 pg/mL [273-410], P = .56) were unchanged. Plasma BNP was increased at all sampling sites in patients with HF as compared with controls. A step down from CS to Ao to RV in all subjects was observed. The step down in apelin from CS to Ao (470 pg/mL [310-595] vs. 320 pg/mL [225-482], P < .04) in control subjects was not apparent in patients with HF. These novel data show that apelin is produced in the human heart and that production is reduced in individuals with HF. In contrast to BNP, apelin production is not exclusive to the heart.
Apelin is a novel endogenous peptide with inotropic and vasodilatory properties that is the ligand for the APJ receptor. Apelin and APJ are widely distributed in the vasculature of a number of organs and peripheral venous apelin is reduced in heart failure (HF). The location of apelin production in humans with and without HF was investigated.BACKGROUNDApelin is a novel endogenous peptide with inotropic and vasodilatory properties that is the ligand for the APJ receptor. Apelin and APJ are widely distributed in the vasculature of a number of organs and peripheral venous apelin is reduced in heart failure (HF). The location of apelin production in humans with and without HF was investigated.Plasma apelin and brain natriuretic peptide (BNP) concentrations in coronary sinus (CS), aorta (Ao), and renal vein (RV) of individuals with HF (n = 9) were compared to subjects with normal structural hearts (n = 8). In HF the concentration of CS apelin was reduced compared with controls (310 pg/mL [interquartile range 290-390] vs. 470 pg/mL [340-570], P < .035) but Ao apelin (330 pg/mL [275-375] vs. 340 pg/mL [230-455], P = .76) and RV apelin (290 pg/mL [280-360] vs. 370 pg/mL [273-410], P = .56) were unchanged. Plasma BNP was increased at all sampling sites in patients with HF as compared with controls. A step down from CS to Ao to RV in all subjects was observed. The step down in apelin from CS to Ao (470 pg/mL [310-595] vs. 320 pg/mL [225-482], P < .04) in control subjects was not apparent in patients with HF.METHODS AND RESULTSPlasma apelin and brain natriuretic peptide (BNP) concentrations in coronary sinus (CS), aorta (Ao), and renal vein (RV) of individuals with HF (n = 9) were compared to subjects with normal structural hearts (n = 8). In HF the concentration of CS apelin was reduced compared with controls (310 pg/mL [interquartile range 290-390] vs. 470 pg/mL [340-570], P < .035) but Ao apelin (330 pg/mL [275-375] vs. 340 pg/mL [230-455], P = .76) and RV apelin (290 pg/mL [280-360] vs. 370 pg/mL [273-410], P = .56) were unchanged. Plasma BNP was increased at all sampling sites in patients with HF as compared with controls. A step down from CS to Ao to RV in all subjects was observed. The step down in apelin from CS to Ao (470 pg/mL [310-595] vs. 320 pg/mL [225-482], P < .04) in control subjects was not apparent in patients with HF.These novel data show that apelin is produced in the human heart and that production is reduced in individuals with HF. In contrast to BNP, apelin production is not exclusive to the heart.CONCLUSIONSThese novel data show that apelin is produced in the human heart and that production is reduced in individuals with HF. In contrast to BNP, apelin production is not exclusive to the heart.
Abstract Background Apelin is a novel endogenous peptide with inotropic and vasodilatory properties that is the ligand for the APJ receptor. Apelin and APJ are widely distributed in the vasculature of a number of organs and peripheral venous apelin is reduced in heart failure (HF). The location of apelin production in humans with and without HF was investigated. Methods and Results Plasma apelin and brain natriuretic peptide (BNP) concentrations in coronary sinus (CS), aorta (Ao), and renal vein (RV) of individuals with HF (n = 9) were compared to subjects with normal structural hearts (n = 8). In HF the concentration of CS apelin was reduced compared with controls (310 pg/mL [interquartile range 290-390] vs. 470 pg/mL [340-570], P < .035) but Ao apelin (330 pg/mL [275-375] vs. 340 pg/mL [230-455], P = .76) and RV apelin (290 pg/mL [280-360] vs. 370 pg/mL [273-410], P = .56) were unchanged. Plasma BNP was increased at all sampling sites in patients with HF as compared with controls. A step down from CS to Ao to RV in all subjects was observed. The step down in apelin from CS to Ao (470 pg/mL [310-595] vs. 320 pg/mL [225-482], P < .04) in control subjects was not apparent in patients with HF. Conclusions These novel data show that apelin is produced in the human heart and that production is reduced in individuals with HF. In contrast to BNP, apelin production is not exclusive to the heart.
Author McDonagh, Theresa A.
Kalra, Paul R.
Hooper, James
Donovan, Jackie
Chandrasekaran, Badrinathan
Clague, Jonathon R.
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Cites_doi 10.1161/CIRCRESAHA.107.158659
10.1016/j.regpep.2003.11.002
10.1016/j.yjmcc.2006.07.004
10.1074/jbc.M908417199
10.1161/01.CIR.0000091235.94914.75
10.1016/j.jacc.2008.06.013
10.1016/S0167-4781(00)00072-5
10.1161/01.CIR.90.1.195
10.1161/01.RES.0000033522.37861.69
10.1016/0378-1119(93)90495-O
10.1006/bbrc.1998.9489
10.1016/j.regpep.2005.09.032
10.1016/j.ejheart.2008.06.002
10.1016/j.ejheart.2005.10.007
10.1093/eurheartj/ehi648
10.1016/j.ejheart.2006.06.005
10.1016/S0167-0115(01)00236-1
10.1016/j.lfs.2006.03.040
10.1046/j.1471-4159.2000.0740034.x
10.1016/S0167-4889(00)00143-9
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Keywords heart failure
brain natriuretic peptide (BNP)
Apelin
Language English
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References Iwanaga, Kihara, Takenaka, Kita (bib10) 2006; 41
Ellinor, Low, MacRae (bib15) 2006; 27
Tatemoto, Hosoya, Habata, Fujii, Kakegawa, Zou (bib2) 1998; 251
O'Dowd, Heiber, Chan, Heng, Tsui, Kennedy (bib1) 1993; 136
Zhang, Ren, Qi, Lou, Chen, Zhang (bib11) 2006; 79
Berry, Pirolli, Jayasankar, Burdick, Morine, Gardner (bib3) 2004; 110
Lee, Cheng, Nguyen, Fan, Kariyawasam, Liu (bib4) 2000; 74
Chong, Gardner, Morton, Ashley, McDonagh (bib12) 2006; 8
Hosoya, Kawamata, Fukusumi, Fujii, Habata, Hinuma (bib6) 2000; 275
Kawamata, Habata, Fukusumi, Hosoya, Fujii, Hinuma (bib7) 2001; 1538
Kleinz, Davenport (bib16) 2004; 118
O'Carroll, Selby, Palkovits, Lolait (bib5) 2000; 1492
Tatemoto, Takayama, Zou, Kumaki, Zhang, Kumano (bib8) 2001; 99
Chen, Ashley, Deng, Tsalenko, Deng, Tabibiazar (bib13) 2003; 108
Chandrasekaran, Dar, McDonagh (bib17) 2008; 10
Szokodi, Tavi, Foldes, Voutilainen-Myllyla, Ilves, Tokola (bib18) 2002; 91
Yasue, Yoshimura, Sumida, Kikuta, Kugiyama, Jougasaki (bib14) 1994; 90
Japp, Cruden, Amer, Li, Goudie, Johnston (bib9) 2008; 52
Goetze, Rehfeld, Carlsen, Videbaek, Andersen, Boesgaard (bib21) 2006; 133
Francia, Salvati, Balla, De Paolis, Pagannone, Borro (bib20) 2007; 9
Kuba, Zhang, Imai, Arab, Chen, Maekawa (bib19) 2007; 101
Kawamata (10.1016/j.cardfail.2010.02.004_bib7) 2001; 1538
Japp (10.1016/j.cardfail.2010.02.004_bib9) 2008; 52
Chong (10.1016/j.cardfail.2010.02.004_bib12) 2006; 8
O'Dowd (10.1016/j.cardfail.2010.02.004_bib1) 1993; 136
Chandrasekaran (10.1016/j.cardfail.2010.02.004_bib17) 2008; 10
Hosoya (10.1016/j.cardfail.2010.02.004_bib6) 2000; 275
Kleinz (10.1016/j.cardfail.2010.02.004_bib16) 2004; 118
Zhang (10.1016/j.cardfail.2010.02.004_bib11) 2006; 79
Yasue (10.1016/j.cardfail.2010.02.004_bib14) 1994; 90
Szokodi (10.1016/j.cardfail.2010.02.004_bib18) 2002; 91
Kuba (10.1016/j.cardfail.2010.02.004_bib19) 2007; 101
Tatemoto (10.1016/j.cardfail.2010.02.004_bib8) 2001; 99
Chen (10.1016/j.cardfail.2010.02.004_bib13) 2003; 108
Ellinor (10.1016/j.cardfail.2010.02.004_bib15) 2006; 27
Francia (10.1016/j.cardfail.2010.02.004_bib20) 2007; 9
Tatemoto (10.1016/j.cardfail.2010.02.004_bib2) 1998; 251
Iwanaga (10.1016/j.cardfail.2010.02.004_bib10) 2006; 41
O'Carroll (10.1016/j.cardfail.2010.02.004_bib5) 2000; 1492
Goetze (10.1016/j.cardfail.2010.02.004_bib21) 2006; 133
Berry (10.1016/j.cardfail.2010.02.004_bib3) 2004; 110
Lee (10.1016/j.cardfail.2010.02.004_bib4) 2000; 74
References_xml – volume: 251
  start-page: 471
  year: 1998
  end-page: 476
  ident: bib2
  article-title: Isolation and characterization of a novel endogenous peptide ligand for the human APJ receptor
  publication-title: Biochem Biophys Res Commun
– volume: 52
  start-page: 908
  year: 2008
  end-page: 913
  ident: bib9
  article-title: Vascular effects of apelin in vivo in man
  publication-title: J Am Coll Cardiol
– volume: 90
  start-page: 195
  year: 1994
  end-page: 203
  ident: bib14
  article-title: Localization and mechanism of secretion of B-type natriuretic peptide in comparison with those of A-type natriuretic peptide in normal subjects and patients with heart failure
  publication-title: Circulation
– volume: 1538
  start-page: 162
  year: 2001
  end-page: 171
  ident: bib7
  article-title: Molecular properties of apelin: tissue distribution and receptor binding
  publication-title: Biochim Biophys Acta
– volume: 108
  start-page: 1432
  year: 2003
  end-page: 1439
  ident: bib13
  article-title: Novel role for the potent endogenous inotrope apelin in human cardiac dysfunction
  publication-title: Circulation
– volume: 27
  start-page: 222
  year: 2006
  end-page: 226
  ident: bib15
  article-title: Reduced apelin levels in lone atrial fibrillation
  publication-title: Eur Heart J
– volume: 10
  start-page: 725
  year: 2008
  end-page: 732
  ident: bib17
  article-title: The role of apelin in cardiovascular function and heart failure
  publication-title: Eur J Heart Fail
– volume: 74
  start-page: 34
  year: 2000
  end-page: 41
  ident: bib4
  article-title: Characterization of apelin, the ligand for the APJ receptor
  publication-title: J Neurochem
– volume: 8
  start-page: 355
  year: 2006
  end-page: 360
  ident: bib12
  article-title: Plasma concentrations of the novel peptide apelin are decreased in patients with chronic heart failure
  publication-title: Eur J Heart Fail
– volume: 41
  start-page: 798
  year: 2006
  end-page: 806
  ident: bib10
  article-title: Down-regulation of cardiac apelin system in hypertrophied and failing hearts: Possible role of angiotensin II-angiotensin type 1 receptor system
  publication-title: J Mol Cell Cardiol
– volume: 101
  start-page: e32
  year: 2007
  end-page: e42
  ident: bib19
  article-title: Impaired heart contractility in Apelin gene-deficient mice associated with aging and pressure overload
  publication-title: Circ Res
– volume: 275
  start-page: 21061
  year: 2000
  end-page: 21067
  ident: bib6
  article-title: Molecular and functional characteristics of APJ. Tissue distribution of mRNA and interaction with the endogenous ligand apelin
  publication-title: J Biol Chem
– volume: 79
  start-page: 1153
  year: 2006
  end-page: 1159
  ident: bib11
  article-title: Exercise training promotes expression of apelin and APJ of cardiovascular tissues in spontaneously hypertensive rats
  publication-title: Life Sci
– volume: 1492
  start-page: 72
  year: 2000
  end-page: 80
  ident: bib5
  article-title: Distribution of mRNA encoding B78/apj, the rat homologue of the human APJ receptor, and its endogenous ligand apelin in brain and peripheral tissues
  publication-title: Biochim Biophys Acta
– volume: 9
  start-page: 306
  year: 2007
  end-page: 309
  ident: bib20
  article-title: Cardiac resynchronization therapy increases plasma levels of the endogenous inotrope apelin
  publication-title: Eur J Heart Fail
– volume: 136
  start-page: 355
  year: 1993
  end-page: 360
  ident: bib1
  article-title: A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11
  publication-title: Gene
– volume: 118
  start-page: 119
  year: 2004
  end-page: 125
  ident: bib16
  article-title: Immunocytochemical localization of the endogenous vasoactive peptide apelin to human vascular and endocardial endothelial cells
  publication-title: Regul Pept
– volume: 110
  start-page: II187
  year: 2004
  end-page: II193
  ident: bib3
  article-title: Apelin has in vivo inotropic effects on normal and failing hearts
  publication-title: Circulation
– volume: 133
  start-page: 134
  year: 2006
  end-page: 138
  ident: bib21
  article-title: Apelin: a new plasma marker of cardiopulmonary disease
  publication-title: Regul Pept
– volume: 99
  start-page: 87
  year: 2001
  end-page: 92
  ident: bib8
  article-title: The novel peptide apelin lowers blood pressure via a nitric oxide-dependent mechanism
  publication-title: Regul Pept
– volume: 91
  start-page: 434
  year: 2002
  end-page: 440
  ident: bib18
  article-title: Apelin, the novel endogenous ligand of the orphan receptor APJ, regulates cardiac contractility
  publication-title: Circ Res
– volume: 101
  start-page: e32
  year: 2007
  ident: 10.1016/j.cardfail.2010.02.004_bib19
  article-title: Impaired heart contractility in Apelin gene-deficient mice associated with aging and pressure overload
  publication-title: Circ Res
  doi: 10.1161/CIRCRESAHA.107.158659
– volume: 118
  start-page: 119
  year: 2004
  ident: 10.1016/j.cardfail.2010.02.004_bib16
  article-title: Immunocytochemical localization of the endogenous vasoactive peptide apelin to human vascular and endocardial endothelial cells
  publication-title: Regul Pept
  doi: 10.1016/j.regpep.2003.11.002
– volume: 110
  start-page: II187
  issue: Suppl 1
  year: 2004
  ident: 10.1016/j.cardfail.2010.02.004_bib3
  article-title: Apelin has in vivo inotropic effects on normal and failing hearts
  publication-title: Circulation
– volume: 41
  start-page: 798
  year: 2006
  ident: 10.1016/j.cardfail.2010.02.004_bib10
  article-title: Down-regulation of cardiac apelin system in hypertrophied and failing hearts: Possible role of angiotensin II-angiotensin type 1 receptor system
  publication-title: J Mol Cell Cardiol
  doi: 10.1016/j.yjmcc.2006.07.004
– volume: 275
  start-page: 21061
  year: 2000
  ident: 10.1016/j.cardfail.2010.02.004_bib6
  article-title: Molecular and functional characteristics of APJ. Tissue distribution of mRNA and interaction with the endogenous ligand apelin
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M908417199
– volume: 108
  start-page: 1432
  year: 2003
  ident: 10.1016/j.cardfail.2010.02.004_bib13
  article-title: Novel role for the potent endogenous inotrope apelin in human cardiac dysfunction
  publication-title: Circulation
  doi: 10.1161/01.CIR.0000091235.94914.75
– volume: 52
  start-page: 908
  year: 2008
  ident: 10.1016/j.cardfail.2010.02.004_bib9
  article-title: Vascular effects of apelin in vivo in man
  publication-title: J Am Coll Cardiol
  doi: 10.1016/j.jacc.2008.06.013
– volume: 1492
  start-page: 72
  year: 2000
  ident: 10.1016/j.cardfail.2010.02.004_bib5
  article-title: Distribution of mRNA encoding B78/apj, the rat homologue of the human APJ receptor, and its endogenous ligand apelin in brain and peripheral tissues
  publication-title: Biochim Biophys Acta
  doi: 10.1016/S0167-4781(00)00072-5
– volume: 90
  start-page: 195
  year: 1994
  ident: 10.1016/j.cardfail.2010.02.004_bib14
  article-title: Localization and mechanism of secretion of B-type natriuretic peptide in comparison with those of A-type natriuretic peptide in normal subjects and patients with heart failure
  publication-title: Circulation
  doi: 10.1161/01.CIR.90.1.195
– volume: 91
  start-page: 434
  year: 2002
  ident: 10.1016/j.cardfail.2010.02.004_bib18
  article-title: Apelin, the novel endogenous ligand of the orphan receptor APJ, regulates cardiac contractility
  publication-title: Circ Res
  doi: 10.1161/01.RES.0000033522.37861.69
– volume: 136
  start-page: 355
  year: 1993
  ident: 10.1016/j.cardfail.2010.02.004_bib1
  article-title: A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11
  publication-title: Gene
  doi: 10.1016/0378-1119(93)90495-O
– volume: 251
  start-page: 471
  year: 1998
  ident: 10.1016/j.cardfail.2010.02.004_bib2
  article-title: Isolation and characterization of a novel endogenous peptide ligand for the human APJ receptor
  publication-title: Biochem Biophys Res Commun
  doi: 10.1006/bbrc.1998.9489
– volume: 133
  start-page: 134
  year: 2006
  ident: 10.1016/j.cardfail.2010.02.004_bib21
  article-title: Apelin: a new plasma marker of cardiopulmonary disease
  publication-title: Regul Pept
  doi: 10.1016/j.regpep.2005.09.032
– volume: 10
  start-page: 725
  year: 2008
  ident: 10.1016/j.cardfail.2010.02.004_bib17
  article-title: The role of apelin in cardiovascular function and heart failure
  publication-title: Eur J Heart Fail
  doi: 10.1016/j.ejheart.2008.06.002
– volume: 8
  start-page: 355
  year: 2006
  ident: 10.1016/j.cardfail.2010.02.004_bib12
  article-title: Plasma concentrations of the novel peptide apelin are decreased in patients with chronic heart failure
  publication-title: Eur J Heart Fail
  doi: 10.1016/j.ejheart.2005.10.007
– volume: 27
  start-page: 222
  year: 2006
  ident: 10.1016/j.cardfail.2010.02.004_bib15
  article-title: Reduced apelin levels in lone atrial fibrillation
  publication-title: Eur Heart J
  doi: 10.1093/eurheartj/ehi648
– volume: 9
  start-page: 306
  year: 2007
  ident: 10.1016/j.cardfail.2010.02.004_bib20
  article-title: Cardiac resynchronization therapy increases plasma levels of the endogenous inotrope apelin
  publication-title: Eur J Heart Fail
  doi: 10.1016/j.ejheart.2006.06.005
– volume: 99
  start-page: 87
  year: 2001
  ident: 10.1016/j.cardfail.2010.02.004_bib8
  article-title: The novel peptide apelin lowers blood pressure via a nitric oxide-dependent mechanism
  publication-title: Regul Pept
  doi: 10.1016/S0167-0115(01)00236-1
– volume: 79
  start-page: 1153
  year: 2006
  ident: 10.1016/j.cardfail.2010.02.004_bib11
  article-title: Exercise training promotes expression of apelin and APJ of cardiovascular tissues in spontaneously hypertensive rats
  publication-title: Life Sci
  doi: 10.1016/j.lfs.2006.03.040
– volume: 74
  start-page: 34
  year: 2000
  ident: 10.1016/j.cardfail.2010.02.004_bib4
  article-title: Characterization of apelin, the ligand for the APJ receptor
  publication-title: J Neurochem
  doi: 10.1046/j.1471-4159.2000.0740034.x
– volume: 1538
  start-page: 162
  year: 2001
  ident: 10.1016/j.cardfail.2010.02.004_bib7
  article-title: Molecular properties of apelin: tissue distribution and receptor binding
  publication-title: Biochim Biophys Acta
  doi: 10.1016/S0167-4889(00)00143-9
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Snippet Apelin is a novel endogenous peptide with inotropic and vasodilatory properties that is the ligand for the APJ receptor. Apelin and APJ are widely distributed...
Abstract Background Apelin is a novel endogenous peptide with inotropic and vasodilatory properties that is the ligand for the APJ receptor. Apelin and APJ are...
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SubjectTerms Apelin
Biomarkers - blood
brain natriuretic peptide (BNP)
Cardiovascular
Female
heart failure
Heart Failure - blood
Heart Failure - complications
Humans
Intercellular Signaling Peptides and Proteins - biosynthesis
Intercellular Signaling Peptides and Proteins - blood
Intercellular Signaling Peptides and Proteins - deficiency
Male
Middle Aged
Myocardium - metabolism
Myocardium - pathology
Natriuretic Peptide, Brain - blood
Systole
Ventricular Dysfunction, Left - blood
Ventricular Dysfunction, Left - complications
Title Myocardial Apelin Production is Reduced in Humans With Left Ventricular Systolic Dysfunction
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https://www.clinicalkey.es/playcontent/1-s2.0-S1071916410000679
https://dx.doi.org/10.1016/j.cardfail.2010.02.004
https://www.ncbi.nlm.nih.gov/pubmed/20610231
https://www.proquest.com/docview/733654470
Volume 16
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