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Effects of combined inhibition of the Na+–H+ exchanger and angiotensin-converting enzyme in rats with congestive heart failure after myocardial infarction

机译:心肌梗死后充血性心力衰竭对Na + –H +交换子和血管紧张素转化酶的联合抑制作用

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class="enumerated" style="list-style-type:decimal">We investigated the single vs the combined long-term inhibition of Na+–H+ exchanger-1 (NHE-1) and ACE in rats with congestive heart failure induced by myocardial infarction (MI).Rats with MI were randomized to receive either placebo, cariporide (3000 p.p.m. via chow), ramipril (1 mg kg−1 day−1 via drinking water) or their combination for 18 weeks starting on day 3 after surgery.Cardiac morphology and function was assessed by echocardiography and by means of a 2.0 F conductance catheter to determine left ventricular (LV) pressure volume relationships.MI for 18 weeks resulted in an increase in LV end-diastolic diameter (LVDed) in the placebo-treated group when compared to sham (placebo: 1.1±0.04 cm; sham: 0.86±0.01; P<0.05). Combined inhibition of NHE-1 and ACE, but not the monotherapies, significantly reduced LVDed (1.02±0.02 cm).Preload recruitable stroke work (PRSW), dp/dtmax (parameter of systolic function) and end-diastolic pressure volume relationship (EDPVR, diastolic function) were significantly impaired in placebo-treated MI group (PRSW: 39±7 mmHg; dp/dtmax: 5185±363 mmHg s−1; EDPVR: 0.042±0.001 mmHg μl−1; all P<0.05). Cariporide treatment significantly improved PRSW (64±7 mmHg), dp/dtmax (8077±525 mmHg s−1) and EDPVR (0.026±0.014 mmHg μl−1), and reduced cardiac hypertrophy in rats with MI. Combined inhibition of NHE-1 and ACE had even a more pronounced effect on PRSW (72±5 mmHg) and EDPVR (0.026±0.014 mmHg μl−1), as well as cardiac hypertrophy that, however, did not reach statistical significance compared to cariporide treatment alone.The NHE-1 inhibitor cariporide significantly improved LV remodeling and function in rats with congestive heart failure induced by MI. The effect of cariporide was comparable or tended to be stronger (e.g. systolic function) compared to ramipril. Combined treatment with cariporide and ramipril tended to be more effective on LV remodeling in rats with heart failure than the single treatments. Thus, inhibition of the NHE-1 may be a promising novel therapeutic approach for the treatment of congestive heart failure.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 我们研究了Na + –H + 交换物-1(NHE-1)和ACE对心肌性充血性心力衰竭大鼠的单一或联合长期抑制作用 患有MI的大鼠随机接受安慰剂,卡立哌利(通过食物3000 ppm),雷米普利(1mgmgkg -1 day -1) (通过饮用水)或其组合,从术后第3天开始持续18周。 通过超声心动图和2.0 aF电导导管评估心脏的形态和功能,以确定左心室(与假手术(安慰剂:1.1±0.04?cm;假手术:)相比,MI持续18周的MI导致安慰剂治疗组的LV舒张末期直径(LVDed)增加。 0.86±0.01; P <0.05)。联合抑制NHE-1和ACE而非单一疗法可显着降低LVDed(1.02±0.02 cm)。 预负荷可招募中风功(PRSW),dp / dtmax(收缩功能参数)和终止安慰剂治疗的MI组患者的舒张压压力关系(EDPVR,舒张功能)明显受损(PRSW:39±7 mmHg; dp / dtmax:5185±363 mmHg s -1 ; EDPVR:0.042 ±0.001 mmHgμl -1 ;所有P <0.05)。 Cariporide治疗可显着改善PRSW(64±7 mmHg),dp / dtmax(8077±525 mmHg s -1 )和EDPVR(0.026±0.014 mmHgμl -1 ),并减少心肌梗死大鼠的心脏肥大。 NHE-1和ACE的联合抑制对PRSW(72±5 mmHg)和EDPVR(0.026±0.014 mmHgμl -1 )以及心脏肥大的影响甚至更为明显,与单独使用卡立哌肽治疗相比,没有统计学意义。 NHI-1抑制剂卡立哌肽显着改善了MI所致充血性心力衰竭大鼠的左室重构和功能。与雷米普利相比,卡立哌肽的作用相当或倾向于更强(例如收缩功能)。与单药相比,卡立哌肽和雷米普利联合治疗对心力衰竭大鼠的左室重塑趋于有效。因此,抑制NHE-1可能是治疗充血性心力衰竭的一种有前途的新治疗方法。

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