The effects of dietary verbascoside on blood and liver oxidative stress status induced by a high n-6 polyunsaturated fatty acids diet in piglets

• Published in: Journal of animal science Vol. 93; no. 6; pp. 2849 - 2859
• Main Authors: Di Giancamillo, A, Rossi, R, Pastorelli, G, Deponti, D, Carollo, V, Casamassima, D, Domeneghini, C, Corino, C
• Format: Journal Article
• Language: English
• Published: United States 01.06.2015
• Subjects: Alanine Transaminase - blood; Animals; Antioxidants - metabolism; Antioxidants - pharmacology; Aspartate Aminotransferases - blood; Blotting, Western - veterinary; Catalase - blood; Diet, High-Fat - veterinary; Dietary Supplements; Fatty Acids, Omega-6 - metabolism; Female; gamma-Glutamyltransferase - blood; Glucosides - administration & dosage; Glucosides - pharmacology; Glutathione Peroxidase - blood; Immunohistochemistry - veterinary; Liver - metabolism; Oxidation-Reduction - drug effects; Oxidative Stress - drug effects; Phenols - administration & dosage; Phenols - pharmacology; Plant Oils - administration & dosage; Sunflower Oil; Superoxide Dismutase - blood; Sus scrofa - metabolism; Swine
• ISSN: 1525-3163
• DOI: 10.2527/jas.2014-8607

Twenty-four weaned female Hypor piglets (10.9 ± 0.1 kg mean BW) were used to evaluate the antioxidant effect of a natural extract, titrated in verbascoside, on blood and liver oxidative status in relation to a high intake of n-6 PUFA, inducing oxidative stress. Piglets were assigned to 1 of 3 experimental groups; the first group was fed a diet with 9% sunflower oil (T1) and the second received the sunflower oil diet supplemented with 5 mg of verbascoside/kg feed from Verbenaceae extract (Lippia spp.; T2). The third group was fed a control diet (CTR), in which an isoenergetic replacement of oil by starch was done. Blood samples were collected at the beginning and the end of the trial (30 d). At the end of the trial, the animals were slaughtered and the liver specimens were collected. Oxidative stress markers, including total antiradical activity, superoxide dismutase (SOD), glutathione peroxidase (GPX), and catalase (CAT) activities, were determined in blood samples. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and γ-glutamyl transferase (GGT) plasma levels were also evaluated. Immunohistochemistry and western blot analyses were performed in liver to evaluate heat shock protein (Hsp) 70, Hsp90, and Kupffer and Ito cell activation. Liver activities of SOD, GPX, and CAT were also determined. Total antiradical activity in blood and red blood cells were affected (P < 0.01) by dietary treatments. The n-6 PUFA supplementation at a high dosage for 30 d induced oxidative stress, decreasing total antiradical activity in blood and red blood cells (CTR vs. T1 + T2; P < 0.01) and plasma CAT activity (CTR vs. T1 + T2; P = 0.088) and increasing ALT value (CTR vs. T1 + T2; P < 0.01). Also, in liver, the CAT and GPX activities tended to be lower in pigs fed n-6 PUFA diets than pigs fed a control diet (CTR vs. T1 + T2; = 0.090 and = 0.085, respectively). The liver samples presented a normal architecture and no Ito and Kupffer cell activations were observed. In liver, the SOD activity tended to be lower in the T1 group (P = 0.064) than in the CTR and T2 groups. Moreover, the level of Hsp70 was higher (P < 0.01) in the T1 group than the CTR and T2 groups. These data suggest that the dose of dietary verbascoside partially restores the antioxidant status of the liver without affecting the systemic responses to oxidative stress induced by a high-fat diet.