The protective effects of an adsorbent against oxidative stress in quails fed aflatoxin-contaminated diet

Migliorini, Marcos José; Silva, Aleksandro Schafer da; Santurio, Janio Morais; Bottari, Nathieli Bianchi; Gebert, Roger Rocha; Reis, João Henrique; Volpato, Andreia; Morsch, Vera Maria; Baldissera, Matheus Dellaméa; Stefani, Lenita Moura; Boiago, Marcel Manete

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The protective effects of an adsorbent against oxidative stress in quails fed aflatoxin-contaminated diet

Migliorini, Marcos JoséSilva, Aleksandro Schafer daSanturio, Janio MoraisBottari, Nathieli BianchiGebert, Roger RochaReis, João HenriqueVolpato, AndreiaMorsch, Vera MariaBaldissera, Matheus DellaméaStefani, Lenita MouraBoiago, Marcel Manete

Background: Contamination of crops with aflatoxin is considered a serious global threat to food safety, since potent carcinogenic, teratogenic, mutagenic and immunosuppressive effects of aflatoxins are well recognized. Recently, the use of adsorbents has been linked with protective effects against oxidative stress in several diseases. Thus, the aim of this study was to assess the occurrence of oxidative stress in quails (Coturnix coturnix) fed with aflatoxin-contaminated diet, as well as the protective effect of an adsorbent.Materials, Methods & Results: Twenty-eight quails were divided into four groups (n = 7): diet without additives (control; the group A), diet and adsorbent containing aluminosilicates (the group B), aflatoxin-contaminated diet (200 ppb) (the group C), and aflatoxin-contaminated diet (200 ppb) and adsorbent containing aluminosilicates (the group D). The composition of the adsorbent containing aluminosilicates was 0.3% based on yeast cell wall, silymarin, and bentonite. The animals received feed and water ad libitum during 20 days. At the end of the experimental period, total blood was collected by cardiac puncture in tubes without anticoagulant to obtain serum (centrifuged at 3500 g during 10 min) for later determination of biochemical parameters. The liver was placed in a solution of TrisHCl 10 mM, pH 7.4 for TBARS (Thiobarbituric acid reactive substances), ROS (Reactive oxygen species), SOD (Superoxide dismutase) and CAT (Catalase) analysis. The hepatic tissue was gently homogenized in a glass potter in specific buffer, homogenated, and centrifuged at 10.000 g at 4ºC for 10 min to yield a supernatant (S1) used for analyses. Homogenate aliquots were stored at -80°C until utilization. Fragments of liver and intestine (5 cm) were collected for histopathological analyses. Between days 15 to 20 of the experiment, group C quails showed clinical signs, such as apathy, creepy feathers and reduced feed intake.[...](AU)