Omega 3 Fatty Acid Inhibition of Inflammatory Cytokine-Mediated Connexin43 Regulation in the Heart

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Omega 3 Fatty Acid Inhibition of Inflammatory Cytokine-Mediated Connexin43 Regulation in the Heart

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Title: Omega 3 Fatty Acid Inhibition of Inflammatory Cytokine-Mediated Connexin43 Regulation in the Heart
Author: Baum, Jennifer R.; Duffy, Heather S.; Dolmatova, Elena; Tan, Alex Yu Hong

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Citation: Baum, Jennifer R., Elena Dolmatova, Alex Yu Hong Tan, and Heather S. Duffy. 2012. Omega 3 fatty acid inhibition of inflammatory cytokine-mediated Connexin43 regulation in the heart. Frontiers in Physiology 3:272.
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Abstract: Background: The proinflammatory cytokine \(Interleukin-1\beta\) \((IL-1\beta)\), which increases in the heart post myocardial infarction (MI), has been shown to cause loss of Connexin43 (Cx43) function, an event known to underlie formation of the arrhythmogenic substrate. Omega 3 Fatty acids exhibit antiarrhythmic properties and impact \(IL-1\beta\) signaling. We hypothesize that Omega-3 fatty acids prevent arrhythmias in part, by inhibiting \(IL-1\beta\) signaling thus maintaining functional Cx43 channels. Methods: Rat neonatal myocytes or Madin-Darby Canine Kidney Epithelial (MDCK) cells grown in media in the absence (Ctr) or presence of \(30 \mu M\) docosahexaenoic acid (DHA, an Omega-3 Fatty acid) were treated with \(0.1 \mu M\) activated \(IL-1\beta\). We determined Cx43 channel function using a dye spread assay. Western blot and immunostaining were used to examine Cx43 levels/localization and downstream effectors of \(IL-1\beta\). In addition we used a murine model of MI for 24 h to determine the impact of an Omega-3 fatty acid enriched diet on Cx43 levels/localization post MI. Results: \(IL-1\beta\) significantly inhibited Cx43 function in Ctr cells \((200.9 \pm 17.7 \mu m [Ctr] vs. 112.8 \pm 14.9 \mu m [0.1 \mu M IL-1\beta], p<0.05)\). However, DHA-treated cells remained highly coupled in the presence of \(IL-1\beta\) \([167.9 \pm 21.9 \mu m [DHA] vs. 164.4 \pm 22.3 \mu m [DHA + 0.1 \ muM IL-1\beta], p<0.05, n = 4]\). Additionally, western blot showed that \(IL-1\beta\) treatment caused a 38.5% downregulation of Cx43 \([1.00 au [Ctr] vs. 0.615 au (0.1 \mu M IL-1\beta)\) which was completely abolished in DHA-treated cells \((0.935 au [DHA] vs. 1.02 au [DHA + 0.1 \mu M IL-1\beta), p < 0.05, n = 3]\). Examination of the downstream modulator of \(IL-1\beta\), \(NF\kappa \beta\) showed that while hypoxia caused translocation of \(NF\kappa \beta\) to the nucleus, this was inhibited by DHA. Additionally we found that a diet enriched in Omega-3 Fatty acids inhibited lateralization of Cx43 in the post-MI murine heart as well as limited activation of fibroblasts which would lead to decreased fibrosis overall. Conclusions: Omega 3 Fatty acid treatment inhibited \(IL-1\beta\)-stimulated loss of Cx43 protein, and more importantly, inhibited loss of Cx43 function by inhibiting translocation of \(NF\kappa \beta\). In the intact heart a diet enriched in Omega 3 Fatty Acids limited loss of Cx43 at the intercalated disk in the heart following MI. These data suggest that one of cardio-protective mechanisms by which Omega 3 Fatty acids work includes prevention of the pro-arrhythmic loss of Cx43 post MI and the attenuation of cardiac fibrosis after injury.
Published Version: doi:10.3389/fphys.2012.00272
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429046
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10352024
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