Spontaneous Atrial Fibrillation in Transgenic Goats With TGF (Transforming Growth Factor)-β1 Induced Atrial Myopathy With Endurance Exercise.

M. Regouski, O. Galenko, Jason Doleac, A. Olsen, Victoria Jacobs, D. Liechty, K. White, T. Bunch, Pamela M Lee, H. Rutigliano, I. Polejaeva, M. Cutler
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引用次数: 10

Abstract

BACKGROUND There is increasing evidence that endurance exercise is associated with increased risk of atrial fibrillation (AF). However, it is unknown if the relationship between endurance exercise and AF is dependent on an atrial myopathy. METHODS Six cardiac-specific TGF (transforming growth factor)-β1 transgenic and 6 wild-type (WT) goats were utilized for these studies. Pacemakers were implanted in all animals for continuous arrhythmia monitoring and AF inducibility. AF inducibility was evaluated using 5 separate 10 s bursts of atrial pacing (160-200 ms). Three months of progressive endurance exercise (up to 90 minutes at 4.5 mph) was performed. Quantitative assessment of circulating microRNAs and inflammatory biomarkers was performed. RESULTS Sustained AF (≥30 s) was induced with 10 s of atrial pacing in 4 out of 6 transgenic goats compared with 0 out of 6 WT controls at baseline (P<0.05). No spontaneous AF was observed at baseline. Interestingly, between 2 and 3 months of exercise 3 out of 6 transgenic animals developed self-terminating spontaneous AF compared with 0 out of 6 WT animals (P<0.05). There was an increase in AF inducibility in both transgenic and WT animals during the first 2 months of exercise with partial normalization at 3 months (transgenic 67%; 100%; 83% versus WT 0%; 67%; 17%). These changes in AF susceptibility were associated with a decrease in circulating microRNA-21 and microRNA-29 during the first 2 months of exercise with partial normalization at 3 months in both transgenic and WT animals. Finally, MMP9 (matrix metallopeptidase 9) was increased during the second and third months of exercise training. CONCLUSIONS This study demonstrates a novel transgenic goat model of cardiac fibrosis (TGF-β1 overexpression) to demonstrate that endurance exercise in the setting of an underlying atrial myopathy increases the incidence of spontaneous AF. Furthermore, endurance exercise seems to increase inducible AF secondary to altered expression of key profibrotic biomarkers that is independent of the presence of an atrial myopathy.
TGF(转化生长因子)-β1转基因山羊自发性心房颤动与耐力运动
背景:越来越多的证据表明,耐力运动与房颤(AF)风险增加有关。然而,目前尚不清楚耐力运动和房颤之间的关系是否依赖于心房肌病。方法选用6只心脏特异性TGF(转化生长因子)-β1转基因山羊和6只野生型山羊进行实验。所有动物均植入起搏器,用于持续监测心律失常和AF诱导。采用5次单独的10 s心房起搏(160-200 ms)评估心房颤动诱发性。进行了三个月的渐进式耐力锻炼(以4.5英里/小时的速度长达90分钟)。定量评估循环microrna和炎症生物标志物。结果6只转基因山羊中有4只在10秒心房起搏后诱发持续性房颤(≥30秒),而对照组6只中0只(P<0.05)。基线时未观察到自发性房颤。有趣的是,在2至3个月的运动期间,6只转基因动物中有3只发生了自终止性自发性房颤,而6只WT动物中没有发生(P<0.05)。在运动的前2个月,转基因和WT动物的AF诱导率都有所增加,3个月时部分正常化(转基因67%;100%;83% vs WT 0%;67%;17%)。这些AF易感性的变化与运动前2个月循环microRNA-21和microRNA-29的减少有关,转基因和WT动物在运动后3个月部分恢复正常。最后,MMP9(基质金属肽酶9)在运动训练的第二和第三个月增加。结论:本研究建立了一种新的转基因山羊心肌纤维化模型(TGF-β1过表达),证明了在潜在心房肌病的情况下,耐力运动增加了自发性房颤的发生率。此外,耐力运动似乎增加了诱导性房颤,继发于与心房肌病存在无关的关键纤维化生物标志物的表达改变。
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