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长期重复阻塞性睡眠呼吸暂停促进大鼠心房颤动。

Atrial fibrillation promotion with long-term repetitive obstructive sleep apnea in a rat model.

机构信息

Department of Medicine, Montréal Heart Institute and Université de Montréal, Montreal, Quebec, Canada; Department of Cardiovascular Medicine, Nippon Medical School, Tokyo, Japan.

Department of Medicine, Montréal Heart Institute and Université de Montréal, Montreal, Quebec, Canada.

出版信息

J Am Coll Cardiol. 2014 Nov 11;64(19):2013-23. doi: 10.1016/j.jacc.2014.05.077. Epub 2014 Nov 3.

Abstract

BACKGROUND

Obstructive sleep apnea (OSA) importantly contributes to the occurrence of atrial fibrillation (AF) in humans, but the mechanisms are poorly understood. Experimental research has provided insights into AF promotion by acute OSA episodes. However, patients with OSA usually have frequent nocturnal episodes for some time before manifesting AF.

OBJECTIVES

The goal of this study was to test the hypothesis that repetitive OSA causes cardiac remodeling that predisposes to AF.

METHODS

We mimicked OSA by using a mechanical ventilator and closing the airway at end-expiration with a 3-way stopcock (OSA rats). Matched control groups included rats with the ventilator stopped but airway left open (open airway rats) and continuously ventilated rats (sham rats). OSA rats were exposed to 20 consecutive 2-min cycles of 40 s of apnea/80 s of ventilation per day, 5 days per week for 4 weeks.

RESULTS

OSA significantly increased the duration of AF from (median [interquartile range]) 2.6 s [1.9 s to 8.9 s] (shams) and 16 s [1.8 s to 93 s] (open airway) to 49s [34 s to 444 s]. AF inducibility increased to 56% (9 of 16) of OSA rats; this is up from 15% (2 of 13) and 13% (2 of 15) in open airway and sham rats, respectively (p < 0.05). OSA rats exhibited substantial atrial conduction slowing on optical mapping, along with connexin-43 down-regulation on both quantitative immunofluorescence (expression reduced by 58% vs sham rats) and Western blot (reduced by 38%), as well as increased atrial fibrous tissue content (by 71%). OSA also caused left ventricular hypertrophy, dilation, and diastolic dysfunction and enhanced AF inducibility during superimposed acute OSA episodes to 82.4% of rats.

CONCLUSIONS

Chronically repeated OSA episodes cause AF-promoting cardiac remodeling, with conduction abnormalities related to connexin dysregulation and fibrosis playing a prominent role. This novel animal model provides mechanistic insights into an important clinical problem and may be useful for further exploration of underlying mechanisms and therapeutic approaches.

摘要

背景

阻塞性睡眠呼吸暂停(OSA)是导致人类心房颤动(AF)发生的重要原因,但机制尚不清楚。实验研究为急性 OSA 发作引起 AF 提供了一些见解。然而,患有 OSA 的患者通常在出现 AF 之前会有一段时间出现频繁的夜间发作。

目的

本研究旨在验证反复性 OSA 引起心脏重构从而导致 AF 的假说。

方法

我们使用机械呼吸机并通过三通阀在呼气末关闭气道来模拟 OSA(OSA 大鼠)。匹配的对照组包括呼吸机停止但气道仍保持开放的大鼠(开放气道大鼠)和持续通气的大鼠(假手术大鼠)。OSA 大鼠每天接受 20 个连续的 2 分钟周期,每个周期包括 40 秒的呼吸暂停和 80 秒的通气,每周 5 天。

结果

OSA 显著增加了 AF 的持续时间,从(中位数[四分位数范围])2.6 秒[1.9 秒至 8.9 秒](假手术)和 16 秒[1.8 秒至 93 秒](开放气道)增加至 49 秒[34 秒至 444 秒]。AF 的诱导率增加到 56%(16 只大鼠中的 9 只);与开放气道和假手术大鼠的 15%(13 只大鼠中的 2 只)和 13%(15 只大鼠中的 2 只)相比,这一比例显著增加(p<0.05)。OSA 大鼠在光学图谱上表现出明显的心房传导减慢,同时定量免疫荧光(与假手术大鼠相比,表达减少 58%)和 Western blot(减少 38%)上的连接蛋白 43 下调,以及心房纤维组织含量增加(增加 71%)。OSA 还导致左心室肥厚、扩张和舒张功能障碍,并在叠加急性 OSA 发作期间增强了 82.4%大鼠的 AF 诱导率。

结论

慢性反复性 OSA 发作导致促 AF 心脏重构,传导异常与连接蛋白失调和纤维化有关。这种新的动物模型为一个重要的临床问题提供了机制上的见解,并可能有助于进一步探索潜在的机制和治疗方法。

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