Key result
Repetitive obstructive sleep apnea increases AF inducibility to ~56% in rats.
Why the study?
Obstructive sleep apnea promotes AF in humans but mechanisms are poorly understood, and the effects of long-term repetitive episodes prior to manifestation remain unclear.
Answers are grounded in this paper and cite their sources.
Demonstrates cardiac remodeling leading to atrial fibrillation in rats exposed to obstructive sleep apnea, suggesting potential therapeutic insights.
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.
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Iwasaki et al. (2014) studied Atrial Fibrillation (n=44). Repetitive Obstructive Sleep Apnea (OSA) model vs. Open airway rats and continuously ventilated sham rats was evaluated on Atrial fibrillation inducibility (p=< 0.05). Repetitive obstructive sleep apnea significantly increased atrial fibrillation inducibility to 56% compared to 15% in open airway and 13% in sham rats (p < 0.05).
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