Tsukashita Masaki, Marui Akira, Nishina Takeshi, Yoshikawa Eiji, Kanemitsu Hideo, Wang Jian, Ikeda Tadashi, Komeda Masashi
Department of Cardiovascular Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
J Thorac Cardiovasc Surg. 2008 Jul;136(1):58-64. doi: 10.1016/j.jtcvs.2007.11.016. Epub 2008 May 7.
Although left ventricular restoration is effective for treating ischemic cardiomyopathy caused by left ventricular remodeling and redilation, the initial improvement in left ventricular function is not always sustained. We have reported that the inhibition of the renin-angiotensin-aldosterone system by angiotensin-converting enzyme inhibitors and angiotensin receptor blockers is effective in preventing late remodeling after left ventricular restoration. However, the effects of spironolactone--an aldosterone blocker--after left ventricular restoration have not been elucidated.
Myocardial infarction was induced by ligating the left anterior descending artery. The rats developed left ventricular aneurysms and underwent left ventricular restoration by the plication of the left ventricular aneurysm 4 weeks after the ligation. Thereafter, the rats were randomized into a left ventricular restoration (vehicle) group and left ventricular restoration with spironolactone (100 mg/kg/d, by mouth) group.
Echocardiography revealed that in the left ventricular restoration with spironolactone group, late cardiac redilation was significantly attenuated (left ventricular end-diastolic area: 0.51 +/- 0.03 cm(2) vs 0.63 +/- 0.03 cm(2), P < .05) and late left ventricular function was preserved (fractional area change: 48.8% +/- 3.0% vs 35.8% +/- 2.4%, P < .01). Hemodynamically, rats in the left ventricular restoration with spironolactone group exhibited improved systolic function (maximal end-systolic pressure-volume relationship: 0.38 +/- 0.03 mm Hg/microL vs 0.11 +/- 0.04 mm Hg/microL, P < .01) and diastolic function (tau: 18.5 +/- 1.5 sec vs 23.1 +/- 1.4 sec, P < .05) than those in the LVR group. Histologically, interstitial fibrosis in the remote area was significantly reduced (5.6% +/- 1.3% vs 12% +/- 1.0%, P < .01), and fibrosis around the pledgets (near area) was also attenuated in the left ventricular restoration with spironolactone group. The myocardial messenger ribonucleic acid expressions of transforming growth factor-beta1 and brain natriuretic peptide measured using the real-time polymerase chain reaction were lower in the left ventricular restoration with spironolactone group (transforming growth factor-beta1: 0.13 +/- 0.02 vs 0.28 +/- 0.02, P < .01; brain natriuretic peptide: 0.99 +/- 0.14 vs 1.54 +/- 0.18, P < .05). The systemic blood pressure and heart rate did not differ between the 2 groups.
Spironolactone reduced the gene expression of transforming growth factor-beta1 and brain natriuretic peptide and alleviated not only cardiac redilation but also the deterioration of left ventricular function late after left ventricular restoration without inducing hypotension, a major side effect of angiotensin-converting enzyme inhibitors or angiotensin receptor blocker. Spironolactone is a promising therapeutic option for alleviating remodeling after left ventricular restoration.
尽管左心室修复术对治疗由左心室重构和再扩张引起的缺血性心肌病有效,但左心室功能的初始改善并不总是能持续。我们曾报道,血管紧张素转换酶抑制剂和血管紧张素受体阻滞剂对肾素 - 血管紧张素 - 醛固酮系统的抑制作用可有效预防左心室修复术后的晚期重构。然而,醛固酮阻滞剂螺内酯在左心室修复术后的作用尚未阐明。
通过结扎左冠状动脉前降支诱导心肌梗死。大鼠形成左心室室壁瘤,并在结扎后4周通过左心室室壁瘤折叠术进行左心室修复。此后,将大鼠随机分为左心室修复(赋形剂)组和左心室修复联合螺内酯(100 mg/kg/d,口服)组。
超声心动图显示,在左心室修复联合螺内酯组中,晚期心脏再扩张明显减轻(左心室舒张末期面积:0.51±0.03 cm²对0.63±0.03 cm²,P <.05),且晚期左心室功能得以保留(面积变化分数:48.8%±3.0%对35.8%±2.4%,P <.01)。血流动力学方面,左心室修复联合螺内酯组大鼠的收缩功能(最大收缩末期压力 - 容积关系:0.38±0.03 mmHg/μL对0.11±0.04 mmHg/μL,P <.01)和舒张功能(时间常数:18.5±1.5秒对23.1±1.4秒,P <.05)均优于左心室修复组。组织学检查显示,远处区域的间质纤维化明显减少(5.6%±1.3%对12%±1.0%),左心室修复联合螺内酯组中补片周围(近处区域)的纤维化也有所减轻。使用实时聚合酶链反应测量的转化生长因子 -β1和脑钠肽的心肌信使核糖核酸表达在左心室修复联合螺内酯组中较低(转化生长因子 -β1:0.13±0.02对0.28±0.02,P <.01;脑钠肽:0.99±0.14对1.54±0.18,P <.05)。两组间的全身血压和心率无差异。
螺内酯降低了转化生长因子 -β1和脑钠肽的基因表达,不仅减轻了心脏再扩张,还缓解了左心室修复术后晚期左心室功能的恶化,且未诱发血管紧张素转换酶抑制剂或血管紧张素受体阻滞剂的主要副作用低血压。螺内酯是减轻左心室修复术后重构的一种有前景的治疗选择。