Medical University of South Carolina, Charleston, 29425, USA.
Circulation. 2010 Jul 6;122(1):20-32. doi: 10.1161/CIRCULATIONAHA.110.936872. Epub 2010 Jun 21.
Disruption of the balance between matrix metalloproteinases (MMP) and MMP inhibitors (TIMPs) within a myocardial infarct (MI) contributes to left ventricular wall thinning and changes in regional stiffness at the MI region. This study tested the hypothesis that a targeted regional approach through localized high-frequency stimulation (LHFS) using low-amplitude electric pulses instituted within a formed MI scar would alter MMP/TIMP levels and prevent MI thinning.
At 3 weeks after MI, pigs were randomized for LHFS (n=7; 240 bpm, 0.8 V, 0.05-ms pulses) or were left unstimulated (UNSTIM; n=10). At 4 weeks after MI, left ventricular wall thickness (echocardiography; 0.89+/-0.07 versus 0.67+/-0.08 cm; P<0.05) and regional stiffness (piezoelectric crystals; 14.70+/-2.08 versus 9.11+/-1.24; P<0.05) were higher with LHFS than in UNSTIM. In vivo interstitial MMP activity (fluorescent substrate cleavage; 943+/-59 versus 1210+/-72 U; P<0.05) in the MI region was lower with LHFS than in UNSTIM. In the MI region, MMP-2 levels were lower and TIMP-1 and collagen levels were higher with LHFS than in UNSTIM (all P<0.05). Transforming growth factor-beta receptor 1 and phosphorylated SMAD-2/3 levels within the MI region were higher with LHFS than in UNSTIM. Electric stimulation (4 Hz) of isolated fibroblasts resulted in reduced MMP-2 and MT1-MMP levels but increased TIMP-1 levels compared with unstimulated fibroblasts.
These unique findings demonstrate that LHFS of the MI region altered left ventricular wall thickness and material properties, likely as a result of reduced regional MMP activity. Thus, LHFS may provide a novel means to favorably modify left ventricular remodeling after MI.
心肌梗死(MI)内基质金属蛋白酶(MMP)和 MMP 抑制剂(TIMPs)之间平衡的破坏导致左心室壁变薄和 MI 区域的局部硬度变化。本研究通过 MI 瘢痕内局部高频刺激(LHFS)用低振幅电脉冲检测假设,即在形成的 MI 瘢痕内实施靶向局部方法会改变 MMP/TIMP 水平并防止 MI 变薄。
在 MI 后 3 周,猪被随机分为 LHFS 组(n=7;240 bpm,0.8 V,0.05-ms 脉冲)或未刺激组(UNSTIM;n=10)。在 MI 后 4 周,与 UNSTIM 相比,LHFS 时左心室壁厚度(超声心动图;0.89+/-0.07 与 0.67+/-0.08 cm;P<0.05)和局部硬度(压电晶体;14.70+/-2.08 与 9.11+/-1.24;P<0.05)更高。MI 区域内 MMP 活性(荧光底物裂解;943+/-59 与 1210+/-72 U;P<0.05)在 LHFS 时低于 UNSTIM。在 MI 区域内,MMP-2 水平低于 UNSTIM,TIMP-1 和胶原水平高于 UNSTIM(均 P<0.05)。与 UNSTIM 相比,MI 区域内转化生长因子-β受体 1 和磷酸化 SMAD-2/3 水平更高。与未刺激的成纤维细胞相比,分离的成纤维细胞的电刺激(4 Hz)导致 MMP-2 和 MT1-MMP 水平降低,但 TIMP-1 水平升高。
这些独特的发现表明,MI 区域的 LHFS 改变了左心室壁厚度和材料特性,可能是由于局部 MMP 活性降低所致。因此,LHFS 可能为 MI 后有利地改变左心室重构提供一种新的方法。