New therapies for the treatment of congestive heart failure

被引:4
作者
Burger, AJ
Burger, MR
Aronson, D
机构
[1] Harvard Univ, Noninvas Cardiol Lab, Beth Israel Deaconess Med Ctr, Sch Med,Div Cardiol, Boston, MA 02215 USA
[2] Rambam Med Ctr, Div Cardiol, Haifa, Israel
关键词
D O I
10.1358/dot.2002.38.1.660506
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Heart failure is characterized by sodium and fluid retention, sympathetic overactivity, parasympathetic withdrawal, vasoconstrictor activation and cytokine elevation. New therapies for heart failure attempt to control neurohormonal activation and limit progressive left ventricular dysfunction. Nesiritide (human B-type natriuretic peptide) is a recently approved new vasodilator that has been given to almost 1,000 patients in numerous clinical investigations; it belongs to a new class of heart failure drugs known as natriuretic peptides. Nesiritide decreases pulmonary capillary wedge pressure, systemic vascular resistance, mean right atrial pressure and pulmonary artery pressure, while improving cardiac index, stroke volume and heart failure symptoms. Many endothelin receptor antagonists are in various stages of development. Early clinical studies have demonstrated beneficial cardiovascular hemodynamic effects. Other new drugs for heart failure also include calcium sensitizers, neutral endopeptidase and vasopeptidase inhibitors, aldosterone receptor antagonists, vasopressin antagonists and cytokine inhibitors. All are being actively investigated and many show significant promise as beneficial therapies in the treatment of heart failure. (C) 2002 Prous Science. All rights reserved.
引用
收藏
页码:31 / 48
页数:18
相关论文
共 118 条
[81]   Effect of age on mortality, hospitalizations and response to digoxin in patients with heart failure: The DIG study [J].
Rich, MW ;
McSherry, F ;
Williford, WO ;
Yusuf, S .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 38 (03) :806-813
[82]   Comparison of vasopeptidase inhibitor, omapatrilat, and lisinopril on exercise tolerance and morbidity in patients with heart failure: IMPRESS randomised trial [J].
Rouleau, JL ;
Pfeffer, MA ;
Stewart, DJ ;
Isaac, D ;
Sestier, F ;
Kerut, EK ;
Porter, CB ;
Proulx, G ;
Qian, CL ;
Block, AJ .
LANCET, 2000, 356 (9230) :615-620
[83]   CLONING OF A CDNA-ENCODING A NON-ISOPEPTIDE-SELECTIVE SUBTYPE OF THE ENDOTHELIN RECEPTOR [J].
SAKURAI, T ;
YANAGISAWA, M ;
TAKUWA, Y ;
MIYAZAKI, H ;
KIMURA, S ;
GOTO, K ;
MASAKI, T .
NATURE, 1990, 348 (6303) :732-735
[84]  
SILVER MA, 1998, J CARD FAIL S, V4, P40
[85]   CELLULAR SIGNALING BY PEPTIDES OF THE ENDOTHELIN GENE FAMILY [J].
SIMONSON, MS ;
DUNN, MJ .
FASEB JOURNAL, 1990, 4 (12) :2989-3000
[86]  
SIMONSON MS, 1993, J BIOL CHEM, V268, P9347
[87]  
Slawsky MT, 2000, CIRCULATION, V102, P2222
[88]   Endothelin receptor antagonists in congestive heart failure:: A new therapeutic principle for the future? [J].
Spieker, LE ;
Noll, G ;
Ruschitzka, FT ;
Lüscher, TF .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 37 (06) :1493-1505
[89]   Inotropic therapy for heart failure [J].
Stevenson, LW .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (25) :1848-1850
[90]   Short-term oral endothelin-receptor antagonist therapy in conventionally treated patients with symptomatic severe chronic heart failure [J].
Sütsch, G ;
Kiowski, W ;
Yan, XW ;
Hunziker, P ;
Christen, S ;
Strobel, W ;
Kim, JH ;
Rickenbacher, P ;
Bertel, O .
CIRCULATION, 1998, 98 (21) :2262-2268