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Dietary Supplementation with Omega-3 Polyunsaturated Fatty Acids Modulate Matrix Metalloproteinase Immunoreactivity in a Mouse Model of Pre-abdominal Aortic Aneurysm
Journal article   Open access   Peer reviewed

Dietary Supplementation with Omega-3 Polyunsaturated Fatty Acids Modulate Matrix Metalloproteinase Immunoreactivity in a Mouse Model of Pre-abdominal Aortic Aneurysm

Kristyn Kavazos, Maria Nataatmadja, Kathryn Wales, Elke Hartland, Chloe Williams and Fraser D Russell
Heart, Lung and Circulation, Vol.24(4), pp.377-385
2015
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https://doi.org/10.1016/j.hlc.2014.11.005View
Published Version

Abstract

abdominal aortic aneurysm matrix metalloproteinases long chain omega-3 polyunsaturated fatty acids transforming growth factor-β1
Background: Two-day infusion of angiotensin II to apolipoprotein E-deficient (ApoE-/-) mice provides a model of pre-abdominal aortic aneurysm. Long chain omega-3 polyunsaturated fatty acids (n-3 PUFAs) have anti-inflammatory effects. This study examined the effect of an eight-week low or high n-3 PUFA diet in ApoE-/- mice on matrix metalloproteinase (MMP) expression and elastin degradation. Methods: ApoE-/- mice were fed a low or high n-3 PUFA diet for eight weeks prior to two-day infusion with angiotensin II. The omega-3 index, MMP-2, MMP-9, TIMP-1, and TGF-β1 immunoreactivity, and elastin fragmentation were measured. Results: The omega-3 index with the low and high n-3 PUFA diet was 3.78% and 13.03%, respectively. MMP-9 immunoreactive stain intensity was lower in mice fed the high, compared to the low n-3 PUFA diet in endothelial cells (suprarenal aorta), and inflammatory cells (suprarenal and infrarenal aorta). Inflammatory cells had higher TIMP-1 and TGF-β1 stain intensity in mice fed the high, compared to the low n-3 PUFA diet (suprarenal aorta). MMP-2 immunoreactivity was unaffected by diet. A non-significant trend for reduced elastin fragmentation was observed in mice fed the high n-3 PUFA diet. Conclusion: Dietary supplementation with n-3 PUFAs may have protective anti-inflammatory effects mediated through modulation of MMPs and TIMPs.

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Cardiac & Cardiovascular Systems

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