Apelin-13 in blood pressure regulation and cardiovascular disease

被引:47
作者
Yamaleyeva, Liliya M. [1 ,2 ]
Shaltout, Hossam A. [1 ,4 ]
Varagic, Jasmina [1 ,2 ,3 ]
机构
[1] Wake Forest Sch Med, Hypertens & Vasc Res Ctr, Winston Salem, NC USA
[2] Wake Forest Sch Med, Dept Surg, Winston Salem, NC USA
[3] Wake Forest Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC USA
[4] Wake Forest Sch Med, Dept Obstet & Gynecol, Winston Salem, NC USA
关键词
apelin; APJ; blood pressure; heart disease; ROSTRAL VENTROLATERAL MEDULLA; ACUTE MYOCARDIAL-INFARCTION; INDUCED HYPERTENSIVE-RATS; ORPHAN RECEPTOR APJ; HEART-FAILURE; ENDOGENOUS LIGAND; POSTMYOCARDIAL INFARCTION; HYPOTENSIVE ACTION; TYPE-1; RECEPTOR; DOWN-REGULATION;
D O I
10.1097/MNH.0000000000000241
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of reviewDespite extensive pharmacological treatment, hypertension and heart failure still pose as high health and economic burden. Thus, novel therapeutic approaches are needed to promote more effective treatment of hypertension and cardiovascular disease. In this review we summarized recent evidence supporting the therapeutic potential of apelin-13, a recently discovered endogenous ligand for the G-protein coupled receptor APJ.Recent findingsSystemic administration of apelin-13 or its posttranslationally modified form, pyroglutamate apelin-13, exert vasodilatory and antihypertensive effects. Yet, central application of apelin increases blood pressure and its systemic effects may be compromised in the presence of endothelial dysfunction. In addition, positive inotropic effects by exogenous apelin in the normal and failing heart, as well as cardioprotective effects after myocardial infarction, strongly suggest its therapeutic potential in preventing and treating heart failure and consequences of myocardial ischemia. However, therapeutic use of apelin is limited primarily by its short half-life and parenteral administration, and significant effort has been directed to the development of novel agonists, delivery methods, and improving the efficacy of agonists at APJ.SummaryThe apelin/APJ axis may represent a new target for the development of novel therapeutic approaches for the treatment of hypertension and cardiovascular disease.
引用
收藏
页码:396 / 403
页数:8
相关论文
共 68 条
[51]   Site-specific effects of apelin-13 in the rat medulla oblongata on arterial pressure and respiration [J].
Seyedabadi, M ;
Goodchild, AK ;
Pilowsky, PM .
AUTONOMIC NEUROSCIENCE-BASIC & CLINICAL, 2002, 101 (1-2) :32-38
[52]   Preferential apelin-13 production by the proprotein convertase PCSK3 is implicated in obesity [J].
Shin, Kyungsoo ;
Pandey, Aditya ;
Liu, Xiang-Qin ;
Anini, Younes ;
Rainey, Jan K. .
FEBS OPEN BIO, 2013, 3 :328-333
[53]   The apelin receptor inhibits the angiotensin II type 1 receptor via allosteric trans-inhibition [J].
Siddiquee, K. ;
Hampton, J. ;
McAnally, D. ;
May, L. T. ;
Smith, L. H. .
BRITISH JOURNAL OF PHARMACOLOGY, 2013, 168 (05) :1104-1117
[54]   Temporal changes in myocardial salvage kinases during reperfusion following ischemia: Studies involving the cardioprotective adipocytokine apelin [J].
Simpkin, James C. ;
Dixon, Richard A. ;
Cooper, Michael B. ;
Yellon, Derek M. .
CARDIOVASCULAR DRUGS AND THERAPY, 2007, 21 (06) :409-414
[55]   Apelin, the novel endogenous ligand of the orphan receptor APJ, regulates cardiac contractility [J].
Szokodi, I ;
Tavi, P ;
Földes, G ;
Voutilainen-Myllyä, S ;
Ilves, M ;
Tokola, H ;
Pikkarainen, S ;
Piuhola, J ;
Rysä, J ;
Tóth, M ;
Ruskoaho, H .
CIRCULATION RESEARCH, 2002, 91 (05) :434-440
[56]   Apelin-13 protects the heart against ischemia-reperfusion injury through inhibition of ER-dependent apoptotic pathways in a time-dependent fashion [J].
Tao, Jianping ;
Zhu, Wei ;
Li, Yapeng ;
Xin, Ping ;
Li, Jing ;
Liu, Mingya ;
Li, Jingbo ;
Redington, Andrew N. ;
Wei, Meng .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2011, 301 (04) :H1471-H1486
[57]   Isolation and characterization of a novel endogenous peptide ligand for the human APJ receptor [J].
Tatemoto, K ;
Hosoya, M ;
Habata, Y ;
Fujii, R ;
Kakegawa, T ;
Zou, MX ;
Kawamata, Y ;
Fukusumi, S ;
Hinuma, S ;
Kitada, C ;
Kurokawa, T ;
Onda, H ;
Fujino, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 251 (02) :471-476
[58]   Hydrolysis of biological peptides by human angiotensin-converting enzyme-related carboxypeptidase [J].
Vickers, C ;
Hales, P ;
Kaushik, V ;
Dick, L ;
Gavin, J ;
Tang, J ;
Godbout, K ;
Parsons, T ;
Baronas, E ;
Hsieh, F ;
Acton, S ;
Patane, M ;
Nichols, A ;
Tummino, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (17) :14838-14843
[59]   Apelin decreases the SR Ca2+ content but enhances the amplitude of [Ca2+]i transient and contractions during twitches in isolated rat cardiac myocytes [J].
Wang, Chen ;
Du, Jun-Feng ;
Wu, Feng ;
Wang, Hai-Chang .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2008, 294 (06) :H2540-H2546
[60]   Plasma apelin concentration is depressed following acute myocardial infarction in man [J].
Weir, Robin A. P. ;
Chong, Kwok Shiong ;
Dalzell, Jonathan R. ;
Petrie, Colin J. ;
Murphy, Charles A. ;
Steedman, Tracey ;
Mark, Patrick B. ;
McDonagh, Theresa A. ;
Dargie, Henry J. ;
McMurray, John J. V. .
EUROPEAN JOURNAL OF HEART FAILURE, 2009, 11 (06) :551-558