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Antioxidative and Antimycotoxigenic Efficacies of Lindl. for Addressing Aflatoxicosis in Cherry Valley Ducks. | LitMetric

AI Article Synopsis

Article Abstract

This study aimed to assess the effectiveness of aflatoxin B (AFB) and extract (TLE) in the diets of Cherry Valley ducklings. Our investigation covered growth indicators, blood biochemical indices, meat quality, intestinal morphology, immune response, and CP450 enzyme-related gene expression. We conducted the study with 180 seven-day-old Cherry Valley ducks, randomly divided into five dietary treatments. These treatments included a basal diet without AFB (T1 group), TLE, or a commercial binder; the basal diet containing 0.1 mg AFB/kg (T2 group), 0.1 mg AFB/kg and 100 mg TLE/kg (T3 group), 0.1 mg AFB/kg and 200 mg TLE/kg (T4 group), and 0.1 mg AFB/kg and 0.5 g/kg of a commercial binder (T5 group), respectively. Ducklings fed with the T2 diet exhibited lower final body weight (BW), average body weight gain (ADG), and poor feed conversion ratio (FCR) during the 42-day trials. However, all ducklings in the T3, T4, and T5 groups showed significant improvements in final BW, ADG, and FCR compared to the T2 group. Increased alanine transaminase (ALT) concentration and increased expression of CYP1A1 and CYP1A2 indicated hepatotoxicity in ducklings fed the T2 diet. In contrast, ducklings fed T3, T4, and T5 diets all showed a decrease in the expression of CYP1A1 and CYP1A2, but only the T4 treatment group showed improvement in ALT concentration. AFB toxicity considerably raised the crypt depth (CD) in both the duodenum and jejunum of the T2 group, while the administration of 200 mg TLE/kg (T4) or a commercial binder (T5) effectively reduced this toxicity. Additionally, the villus width of the jejunum in the T2 treatment group decreased significantly, while all T3, T4, and T5 groups showed improvement in this regard. In summary, extract can detoxify aflatoxicosis, leading to growth reduction and hepatic toxicosis in Cherry Valley ducklings.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11360618PMC
http://dx.doi.org/10.3390/toxins16080334DOI Listing

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