We have previously shown that α-linolenic acid (ALA), a (n-3) PUFA exerts in vitro antiinflammatory effects in the intestine. In this study, we aimed to evaluate its effect on inflammatory and oxidative stress in a colitis model. Colitis was induced in 2 groups at d 0 by intrarectal injection of 2-4-6-trinitrobenzen sulfonic acid (TNBS), whereas the control group received the vehicle. Rats we fed 450 mg . kg(-1) . d(-1) of ALA (TNBS+ALA) while the other colitic group (TNBS) and the control group were fed an isocaloric corn oil formula for 14 d (from d -7 to d 7). RBC fatty acid composition was assessed. Oxidative stress was studied by measuring urinary 8-isoprostanes (8-IP) and colon glutathione (GSH) concentration and inducible nitric oxide synthase (iNOS) expression. Colitis was assessed histologically, by production of proinflammatory mediators, including cytokines, leukotrienes B(4) (LTB(4)), and cyclooxygenase-2 (COX-2) and by nuclear factor-κB (NF-κB) activation. The ALA-rich diet significantly increased the RBC levels of ALA, eicosapentaenoic acid, and docosapentaenoic acid (n-3) compared with the TNBS group (P < 0.01 for all). The beneficial effect of ALA supplementation on oxidative stress was reflected by lower urinary 8-IP levels (P < 0.05), a normalized colon GSH concentration (P < 0.01), and reduced colon iNOS expression (P < 0.05) compared with the TNBS group. ALA also protected against colon inflammation as assessed by lower tumor necrosis factor-α secretion and mRNA level (P < 0.05), reduced NF-κB activation (P = 0.01), and lower colon lipid mediator concentrations such as LTB(4) and COX-2 (P < 0.05) compared with the TNBS group. These findings show that an ALA-rich formula is beneficial to TNBS-induced colitic rats via inhibition of oxidative and inflammatory stress.
Three dimensionally ordered macroporous layered double hydroxides (3-DOM LDH) have been synthesized using sacrificial polystyrene (PS) colloidal crystal templates impregnated by divalent and trivalent metal salts. LDH spatially confined coprecipitation occurs during soaking in NaOH solution, and the PS template is subsequently removed by dissolution to preserve the hydroxyl structure. This synthetic process can be applied to a wide range of LDH compositions (MII: Mg, Ni, Co, Zn and MIII: Al, Cr). On the basis of XRD, SEM, TEM, chemical analysis, nitrogen adsorption, XAS experiments, and TGA, structural, textural, and thermal properties of these new nanostructured LDH particles are described. In particular, the study shows that both macro- and mesoporosity can be present and that the macroporosity is maintained after calcination at temperatures as high as 800 °C, giving rise to the presence of macroporous metal and mixed metal oxides. The photocatalytic activity experiments indicate that decatungstate intercalated into the 3-DOM LDH exhibits a higher photocatalytic activity for the photodegradation of 2,6-dimethylphenol than the decatungstate intercalated into the standard coprecipitated LDH parent material.
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