Department of Medicine, Unit of Cardiology, Karolinska Institutet, D1:04, 171 76 Stockholm, Sweden.
Heart and Vascular Theme, Karolinska University Hospital, Norrbacka, S1:02, 171 76 Stockholm, Sweden.
Eur Heart J. 2023 Jun 9;44(22):2009-2025. doi: 10.1093/eurheartj/ehad100.
Ghrelin is an endogenous appetite-stimulating peptide hormone with potential cardiovascular benefits. Effects of acylated (activated) ghrelin were assessed in patients with heart failure and reduced ejection fraction (HFrEF) and in ex vivo mouse cardiomyocytes.
In a randomized placebo-controlled double-blind trial, 31 patients with chronic HFrEF were randomized to synthetic human acyl ghrelin (0.1 µg/kg/min) or placebo intravenously over 120 min. The primary outcome was change in cardiac output (CO). Isolated mouse cardiomyocytes were treated with acyl ghrelin and fractional shortening and calcium transients were assessed. Acyl ghrelin but not placebo increased cardiac output (acyl ghrelin: 4.08 ± 1.15 to 5.23 ± 1.98 L/min; placebo: 4.26 ± 1.23 to 4.11 ± 1.99 L/min, P < 0.001). Acyl ghrelin caused a significant increase in stroke volume and nominal increases in left ventricular ejection fraction and segmental longitudinal strain and tricuspid annular plane systolic excursion. There were no effects on blood pressure, arrhythmias, or ischaemia. Heart rate decreased nominally (acyl ghrelin: 71 ± 11 to 67 ± 11 b.p.m.; placebo 69 ± 8 to 68 ± 10 b.p.m.). In cardiomyocytes, acyl ghrelin increased fractional shortening, did not affect cellular Ca2+ transients, and reduced troponin I phosphorylation. The increase in fractional shortening and reduction in troponin I phosphorylation was blocked by the acyl ghrelin antagonist D-Lys 3.
In patients with HFrEF, acyl ghrelin increased cardiac output without causing hypotension, tachycardia, arrhythmia, or ischaemia. In isolated cardiomyocytes, acyl ghrelin increased contractility independently of preload and afterload and without Ca2+ mobilization, which may explain the lack of clinical side effects. Ghrelin treatment should be explored in additional randomized trials.
ClinicalTrials.gov Identifier: NCT05277415.
Ghrelin 是一种内源性食欲刺激肽激素,具有潜在的心血管益处。在射血分数降低的心力衰竭(HFrEF)患者和体外小鼠心肌细胞中评估了酰化(激活)ghrelin 的作用。
在一项随机、安慰剂对照、双盲试验中,31 名慢性 HFrEF 患者被随机分为静脉内给予合成人酰基 ghrelin(0.1μg/kg/min)或安慰剂,持续 120 分钟。主要终点是心输出量(CO)的变化。用酰基 ghrelin 处理分离的小鼠心肌细胞,并评估其缩短分数和钙瞬变。酰基 ghrelin 而非安慰剂增加心输出量(酰基 ghrelin:4.08±1.15 至 5.23±1.98 L/min;安慰剂:4.26±1.23 至 4.11±1.99 L/min,P<0.001)。酰基 ghrelin 导致每搏量显著增加,左室射血分数和节段性纵向应变和三尖瓣环平面收缩期位移名义增加。对血压、心律失常或缺血无影响。心率名义上略有下降(酰基 ghrelin:71±11 至 67±11 bpm;安慰剂 69±8 至 68±10 bpm)。在心肌细胞中,酰基 ghrelin 增加缩短分数,不影响细胞 Ca2+瞬变,并减少肌钙蛋白 I 磷酸化。缩短分数的增加和肌钙蛋白 I 磷酸化的减少被酰基 ghrelin 拮抗剂 D-Lys3 阻断。
在 HFrEF 患者中,酰基 ghrelin 增加心输出量而不引起低血压、心动过速、心律失常或缺血。在分离的心肌细胞中,酰基 ghrelin 增加收缩力,不依赖于前负荷和后负荷,并且不动员 Ca2+,这可能解释了缺乏临床副作用的原因。应该在其他随机试验中探索 ghrelin 治疗。
ClinicalTrials.gov 标识符:NCT05277415。