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膳食 ω-3 脂肪酸与室颤易感性:缺乏保护作用和致心律失常作用。

Dietary omega-3 fatty acids and susceptibility to ventricular fibrillation: lack of protection and a proarrhythmic effect.

机构信息

Department of Physiology and Cell Biology, College of Pharmacy, The Ohio State University, Columbus, OH 43210-1218, USA.

出版信息

Circ Arrhythm Electrophysiol. 2012 Jun 1;5(3):553-60. doi: 10.1161/CIRCEP.111.966739. Epub 2012 Feb 14.

Abstract

BACKGROUND

Recent clinical studies that evaluated the effects of supplemental omega-3 polyunsaturated fatty acids (n-3 PUFAs) on sudden cardiac death have yielded conflicting results. Our aim was to clarify this issue using an established and clinical relevant canine model of sudden cardiac death.

METHODS AND RESULTS

Susceptibility to ventricular fibrillation (VF) was evaluated using a 2-minute left circumflex artery occlusion during the last minute of an exercise test in 76 dogs (from 2 independent studies) with healed myocardial infarctions (MI); 44 developed VF (susceptible, VF+), whereas 32 did not (resistant, VF-). These dogs were then randomly assigned to either placebo (1 g/d, corn oil; 15 VF+, 11 VF-) or n-3 PUFA (1-4 g/d, docosahexaenoic acid+eicosapentaenoic acid ethyl esters, 29 VF+, 21 VF-) groups. Seven sham (no-MI) dogs were also treated with n-3 PUFA (4 g/d). After treatment (3 months), the exercise+ischemia test was repeated. Dietary n-3 PUFAs produced significant (P<0.01) increases in red blood cell and left ventricular n-3 PUFA levels. Nine post-MI (5 placebo versus 4 n-3 PUFA) and 2 sham dogs died suddenly during the 3-month treatment period. The n-3 PUFA treatment failed to prevent arrhythmias in VF+ dogs (decreased in 27% placebo versus 24% n-3 PUFA, P=0.5646) but induced VT/VF in VF- animals (n-3 PUFA 33% versus placebo 0%, P=0.0442).

CONCLUSIONS

Despite large increases in cardiac tissue n-3 PUFA content, dietary n-3 PUFAs did not prevent ischemia-induced VF and actually increased arrhythmia susceptibility in both noninfarcted and low-risk post-MI dogs.

摘要

背景

最近评估补充欧米伽-3 多不饱和脂肪酸(n-3 PUFA)对心源性猝死影响的临床研究得出了相互矛盾的结果。我们的目的是使用已建立的且与临床相关的犬心源性猝死模型来阐明这个问题。

方法和结果

在 76 只患有心肌梗死(MI)的狗(来自 2 项独立研究)中,在运动试验的最后 1 分钟进行 2 分钟左回旋支动脉闭塞,评估心室颤动(VF)的易感性;其中 44 只发生 VF(易感性,VF+),32 只未发生 VF(抗性,VF-)。然后,这些狗被随机分配到安慰剂(1 克/天,玉米油;15 只 VF+,11 只 VF-)或 n-3 PUFA(1-4 克/天,二十二碳六烯酸+二十碳五烯酸乙酯,29 只 VF+,21 只 VF-)组。7 只假手术(无 MI)狗也接受 n-3 PUFA(4 克/天)治疗。治疗(3 个月)后,重复运动+缺血试验。饮食 n-3 PUFA 可显著(P<0.01)增加红细胞和左心室 n-3 PUFA 水平。9 只 MI 后(5 只安慰剂与 4 只 n-3 PUFA)和 2 只假手术狗在 3 个月治疗期间突然死亡。n-3 PUFA 治疗未能预防 VF+狗的心律失常(安慰剂组减少 27%,n-3 PUFA 组减少 24%,P=0.5646),但诱导 VF-动物的 VT/VF(n-3 PUFA 33%,安慰剂 0%,P=0.0442)。

结论

尽管心脏组织 n-3 PUFA 含量大幅增加,但饮食 n-3 PUFA 并不能预防缺血引起的 VF,实际上还增加了非梗死和低风险 MI 后狗的心律失常易感性。

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