Current Targets and Future Directions of Positive Inotropes for Heart Failure

被引:2
|
作者
Fairuz, Shadreen [1 ]
Ang, Chee Wei [1 ]
Mraiche, Fatima [2 ]
Goh, Joo Kheng [1 ]
机构
[1] Monash Univ, Sch Sci, Jalan Lagoon Selatan, Subang Jaya 47500, Selangor, Malaysia
[2] Univ Alberta, Dept Pharmacol, 116 St & 85 Av, Edmonton, AB T6G 2R3, Canada
关键词
Positive inotropes; heart failure; myocardial contraction; protein targets; small molecule; organ dysfunction; BIOLOGICAL EVALUATION; DERIVATIVES; RECEPTOR; MODULATION; MECHANISMS; DIGITALIS; SERCA2A; DESIGN; AGENTS; PHOSPHODIESTERASES;
D O I
10.2174/0109298673262360231018193823
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While a congestive heart failure patient will ultimately need an assist device or even a replacement heart as the disease progresses, not every patient is qualified for such advanced therapy. Such patients awaiting better circulatory support benefit from positive inotropes in the meantime as palliative care. These agents are often prescribed in patients with acute decompensated heart failure, with reduced left ventricular ejection fraction and symptoms of organ dysfunction. Although positive inotropes, for example, digoxin, dobutamine, milrinone, levosimendan, etc., are successfully marketed and in use, a lot of their adverse effects, like arrhythmias, hypotension, and even sudden cardiac death, are rather encouraging further research on the development of novel positive inotropes. This review has investigated the molecular mechanisms of some of these adverse effects in terms of the proteins they target, followed by research on newer targets. Studies from 2013-2023 that have reported new small molecules with positive inotropic effects have been revisited in order to determine the progress made so far in drug discovery.
引用
收藏
页码:6971 / 6991
页数:21
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