19 research outputs found

    Hepatic paramters in apoE<sup>-/-</sup> mice fed a high-fat diet (control) or a diet supplemented with 0.3% TTA for 12 weeks.

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    <p>In liver extracts, fatty acids were measured using gas-liquid chromotography, enzyme activities were measured spectrophotometrically and lipid deposition was assessed using Red Oil staining. <b>A</b>) Tetradecylthioacetic aicd and <b>B</b>) TTA:1n-8, <b>C</b>) Carnitine palmitoyltransferase 1a activity, <b>D</b>) carnitine palmitoyltransferase 2 <b>E</b>) 3-hydroxy-3-methylglutaryl coenzyme A synthase activity <b>F</b>) Citrate synthase activity, <b>G</b>) Acyl-coenzyme A oxidase activity, <b>H</b>) Lipids droplets and <b>I</b>) Triacylglycerols. Bars represent means ± SD in 4-6 mice for each diet. Unpaired <i>t</i>-test was used to detect statistical significance and results significantly different from control are indicated *P<0.05, **P<0.01, ***P<0.001.</p

    Levels of mRNA expression in aorta and inflammatory mediators in plasma in apoE<sup>−/−</sup> mice fed a high-fat diet (control) or a diet with 5% SPH for 12 weeks.

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    <p>(A) The gene expressions of the inflammatory markers <i>Icam1</i>, <i>Vcam1</i>, <i>Nos2</i> and <i>Mcp1</i> were measured in pooled aortic arch from six mice. Inflammatory markers in blood samples collected at day 77 of treatment were analysed (B) IL-1β, (C) IL-6, (D) IL-10, (E) TNF-α, (F) GM-CSF and bars represent means ± SD of 4 pooled samples of 3 mice for each diet. Unpaired <i>t</i>-test was used to assess statistical significance and results significantly different from control are indicated (*P<0.05, **P<0.01).</p

    Atherosclerotic plaque level in apoE<sup>−/−</sup> mice fed a high-fat diet (control) or a diet with 5% SPH.

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    <p>After 12 weeks of dietary treatment, whole aorta was collected and <i>en-face</i> analysis was performed to quantify aortic surface covered by atherosclerotic plaques. Bars represent means ± SD of 12 mice for each diet. Unpaired <i>t</i>-test was used to detect statistical significance (*P<0.05).</p

    Plasma concentration of inflammatory mediators in apoE<sup>-/-</sup> mice fed a high-fat diet (control) or a diet supplemented with 0.3% TTA for 11 weeks.

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    <p>Blood samples collected at day 77 of treatment were analysed <b>A</b>) IL-1α, <b>B</b>) IL-6, <b>C</b>) IL-17, <b>D</b>) TNF-α and <b>E</b>) IFN-γ. Bars represent means ± SD for 4 mice for each diet. Unpaired <i>t</i>-test was used to assess statistical significance and results significantly different from control are indicated *P<0.05, **P<0.01, ***P<0.001.</p

    Plasma lipid concentrations of apoE<sup>-/-</sup> mice fed a high-fat diet (control) or a diet supplemented with 0.3% TTA.

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    <p>After 28, 56 and 77 days of diet induction, blood was collected, EDTA plasma was isolated and plasma lipids were determined by enzymatic assay. <b>A</b>) Triacylglycerols, <b>B</b>) Non-esterified fatty acids, <b>C</b>) Cholesterol, <b>D</b>) Free cholesterol, <b>E</b>) High-density lipoprotein cholesterol and <b>F</b>) Low-density lipoprotein cholesterol. Bars represent means ± SD for 4 mice for each diet. Unpaired <i>t</i>-test was used to detect statistical significance and results significantly different from control are indicated *P<0.05, **P<0.01, ***P<0.001.</p
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