Treatment of Chronic Heart Failure With β-Adrenergic Receptor Antagonists A Convergence of Receptor Pharmacology and Clinical Cardiology

被引:133
作者
Bristow, Michael R. [1 ]
机构
[1] Univ Colorado, Div Cardiol, Cardiovasc Inst, Aurora, CO 80045 USA
关键词
heart failure; adrenergic receptors; beta-blockers; norepinephrine; drug development; HUMAN BETA(1)-ADRENERGIC RECEPTOR; CA2+/CALMODULIN-DEPENDENT PROTEIN-KINASE; CYCLIC ADENOSINE-MONOPHOSPHATE; IMPROVES CARDIAC-FUNCTION; LEFT-VENTRICULAR FUNCTION; FAILING HUMAN-HEART; DOUBLE-BLIND; DILATED CARDIOMYOPATHY; MESSENGER-RNA; PLASMA NOREPINEPHRINE;
D O I
10.1161/CIRCRESAHA.111.245092
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite the absence of a systematic development plan, beta-blockers have reached the top tier of medical therapies for chronic heart failure. The successful outcome was due to the many dedicated investigators who produced, over a 30-year period, increasing evidence that beta-blocking agents should or actually did improve the natural history of dilated cardiomyopathies and heart failure. It took 20 years for supportive evidence to become undeniable, at which time in 1993 the formidable drug development resources of large pharmaceutical companies were deployed into Phase 3 trials. Success then came relatively quickly, and within 8 years multiple agents were on the market in the United States and Europe. Importantly, there is ample room to improve antiadrenergic therapy, through novel approaches exploiting the nuances of receptor biology and/or intracellular signaling, as well as through pharmacogenetic targeting. (Circ Res. 2011;109:1176-1194.)
引用
收藏
页码:1176 / 1194
页数:19
相关论文
共 179 条
  • [1] Coordinate changes in myosin heavy chain isoform gene expression are selectively associated with alterations in dilated cardiomyopathy phenotype
    Abraham, WT
    Gilbert, EM
    Lowes, BD
    Minobe, WA
    Larrabee, P
    Roden, RL
    Dutcher, D
    Sederberg, J
    Lindenfeld, JA
    Wolfel, EE
    Shakar, SF
    Ferguson, D
    Volkman, K
    Linseman, JV
    Quaife, RA
    Robertson, AD
    Bristow, MR
    [J]. MOLECULAR MEDICINE, 2002, 8 (11) : 750 - 760
  • [2] A STUDY OF THE ADRENOTROPIC RECEPTORS
    AHLQUIST, RP
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1948, 153 (03): : 586 - 600
  • [3] Cardioprotective and survival benefits of long-term combined therapy with β2 adrenoreceptor (AR) agonist and β1 AR blocker in dilated cardiomyopathy postmyocardial infarction
    Ahmet, Ismayil
    Krawczyk, Melissa
    Zhu, Weizhong
    Woo, Anthony Yiu-Ho
    Morrell, Christopher
    Poosala, Suresh
    Xiao, Riu-Ping
    Lakatta, Edward G.
    Talan, Mark I.
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2008, 325 (02) : 491 - 499
  • [4] Anand I, 2010, J AM COLL CARDIOL, V55, p[A37, E360]
  • [5] A RANDOMIZED TRIAL OF LOW-DOSE BETA-BLOCKADE THERAPY FOR IDIOPATHIC DILATED CARDIOMYOPATHY
    ANDERSON, JL
    LUTZ, JR
    GILBERT, EM
    SORENSEN, SG
    YANOWITZ, FG
    MENLOVE, RL
    BARTHOLOMEW, M
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1985, 55 (04) : 471 - 475
  • [6] CaMKII and a failing strategy for growth in heart
    Anderson, Mark E.
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (05) : 1082 - 1085
  • [7] ANDERSSON B, 1998, LANCET, V351, P1180
  • [8] [Anonymous], 1990, Lancet, V336, P1
  • [9] Dilated cardiomyopathy and sudden death resulting from constitutive activation of protein kinase A
    Antos, CL
    Frey, N
    Marx, SO
    Reiken, S
    Gaburjakova, M
    Richardson, JA
    Marks, AR
    Olson, EN
    [J]. CIRCULATION RESEARCH, 2001, 89 (11) : 997 - 1004
  • [10] EFFECTS OF THE BETA-2-ADRENOCEPTOR ANTAGONIST ICI-118,551 ON EXERCISE TACHYCARDIA AND ISOPRENALINE-INDUCED BETA-ADRENOCEPTOR RESPONSES IN MAN
    ARNOLD, JMO
    OCONNOR, PC
    RIDDELL, JG
    HARRON, DWG
    SHANKS, RG
    MCDEVITT, DG
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1985, 19 (05) : 619 - 630