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首页> 外文期刊>Circulation: An Official Journal of the American Heart Association >Mechanisms of atrial tachyarrhythmias associated with coronary artery occlusion in a chronic canine model.
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Mechanisms of atrial tachyarrhythmias associated with coronary artery occlusion in a chronic canine model.

机译:在慢性犬模型中与冠状动脉闭塞相关的心房性心律失常的机制。

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BACKGROUND: Coronary artery disease predisposes to atrial fibrillation (AF), but the effects of chronic atrial ischemia/infarction on AF-related substrates are unknown. METHODS AND RESULTS: Regional right atrial myocardial infarction (MI) was created in 40 dogs by ligating an artery that supplies the right atrial free wall and not the ventricles; 35 sham dogs with the same artery isolated but not ligated were controls. Dogs were observed 8 days after MI and subjected to open-chest study, in vitro optical mapping, and/or cell isolation for patch-clamp and Ca(2+) imaging on day 8. Holter ECGs showed more spontaneous atrial ectopy in MI dogs (eg, 662+/-281 on day 7 versus 34+/-25 ectopic complexes per day at baseline; 52+/-21 versus 1+/-1 atrial tachycardia episodes per day). Triggered activity was increased in MI border zone cells, which had faster decay of caffeine-evoked Ca(2+) transients and enhanced (by approximately 73%) Na(+)-Ca(2+) exchange current. Spontaneous Ca(2+) sparks (confocal microscopy) occurred under beta-adrenergic stimulation in more MI dog cells (66+/-9%) than in control cells (29+/-4%; P<0.01). Burst pacing induced long-lasting AF in MI dogs (1146+/-259 versus 30+/-14 seconds in shams). Increased border zone conduction heterogeneity was confirmed by both bipolar electrode mapping in vivo and optical mapping. Optical mapping demonstrated stable border zone reentry in all 9 MI preparations but in none of 6 shams. Border zone tissue showed increased fibrous tissue content. CONCLUSIONS: Chronic atrial ischemia/infarction creates substrates for both spontaneous ectopy (Ca(2+)-release events, increased Na(+)-Ca(2+) exchange current) and sustained reentry (conduction abnormalities that anchor reentry). Thus, chronic atrial infarction in dogs promotes both AF triggers and the substrate for AF maintenance. These results provide novel insights into potential AF mechanisms in patients with coronary artery disease.
机译:背景:冠状动脉疾病易诱发心房纤颤(AF),但慢性心房缺血/梗死对AF相关基质的影响尚不清楚。方法和结果:40只狗结扎了一条供应右心房游离壁而不是心室的动脉,从而产生了局部右心房心肌梗塞(MI)。将35只具有相同动脉但未结扎的假狗作为对照。 MI后8天观察狗,并在第8天进行开胸研究,体外光学测绘和/或膜片钳和Ca(2+)成像的细胞分离,动态心电图显示MI狗有更多自发性心房异位(例如,第7天为662 +/- 281,而基线时为每天34 +/- 25异位复合物;每天52 +/- 21,而心房心动过速为1 +/- 1)。 MI边界带细胞中触发的活动增加,它具有咖啡因诱发的Ca(2+)瞬变的更快衰减和增强(大约73%)Na(+)-Ca(2+)交换电流。自发的Ca(2+)火花(锥镜)在β-肾上腺素能刺激下比对照组细胞(29 +/- 4%; P <0.01)更多的MI狗细胞(66 +/- 9%)发生。突发起搏可在MI狗中诱发持久的AF(1146 +/- 259秒,而短毛犬则为30 +/- 14秒)。通过体内双极电极标测和光学标测,证实边界区传导异质性增加。光学测绘显示,在所有9种MI制剂中,边界区的折返稳定,但在6种毛囊中均没有。边界区组织显示纤维组织含量增加。结论:慢性心房缺血/梗塞创建自发性异位(Ca(2 +)-释放事件,Na(+)-Ca(2+)交换电流增加)和持续折返(传导异常,锚定折返)的底物。因此,犬的慢性心梗会促进房颤触发和房颤维持的基质。这些结果为冠心病患者潜在的房颤机制提供了新颖的见解。

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