Circulation Journal
Online ISSN : 1347-4820
Print ISSN : 1346-9843
ISSN-L : 1346-9843
Long-Term Treatment With Eicosapentaenoic Acid Ameliorates Myocardial Ischemia-Reperfusion Injury in Pigs In Vivo
– Involvement of Rho-Kinase Pathway Inhibition –
Jun Yi GaoSatoshi YasudaRyuji TsuburayaYoshitaka ItoTakashi ShirotoKiyotaka HaoKentaro AizawaYoku KikuchiKenta ItoHiroaki Shimokawa
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2011 Volume 75 Issue 8 Pages 1843-1851


Background: Eicosapentaenoic acid (EPA), the major n-3 fatty acid in fish oil, exerts cardioprotective effects against ischemic heart disease; however, the detailed mechanisms remain to be elucidated. Rho-kinase plays an important role in the pathogenesis of cardiovascular diseases including ischemia-reperfusion (I/R) injury. Thus, the hypothesis that long-term EPA treatment ameliorates myocardial I/R injury through Rho-kinase pathway inhibition in pigs in vivo was investigated. Methods and Results: Male pigs were treated with either a control chow or EPA (600·mg·kg-1·day-1) for 3 weeks (n=8 each) and were subjected to myocardial ischemia by 90-min occlusion of the left circumflex coronary artery and subsequent 60-min reperfusion. The EPA group had an increased EPA level in red blood cells (4.4±0.3mol%). The EPA treatment significantly ameliorated myocardial I/R injury, including regional wall motion abnormality (EPA 5.3±3.6 vs. control 35.1±3.8 unit, P<0.0001), left ventricular ejection fraction (EPA 43±9% vs. control 32±7%, P<0.05), occurrence of ventricular arrhythmias (EPA 181±73 vs. control 389±51 events, P<0.0001) and histological accumulation of inflammatory cells (P<0.01). Importantly, the EPA treatment significantly inhibited myocardial Rho-kinase activity (assessed by the extent of the myosin-binding subunit phosphorylation) (EPA 0.47±0.11 vs. control 0.77±0.14, P<0.05) and preserved myocardial eNOS activity (EPA 0.56±0.13 vs. control 0.23±0.07, P<0.01) with a significant correlation noted between them. Conclusions: Long-term treatment with EPA ameliorates I/R injury partly through Rho-kinase pathway inhibition in vivo. (Circ J 2011; 75: 1843-1851)

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