| Autor: |
Jeong JY; Animal Nutrition and Physiology Division, National Institute of Animal Science, Wanju 55365, Republic of Korea., Kim J; Animal Nutrition and Physiology Division, National Institute of Animal Science, Wanju 55365, Republic of Korea., Kim M; Animal Nutrition and Physiology Division, National Institute of Animal Science, Wanju 55365, Republic of Korea., Shim SH; Animal Nutrition and Physiology Division, National Institute of Animal Science, Wanju 55365, Republic of Korea., Park C; Division of Animal Science, College of Agriculture and Life Sciences, Chonnam National University, Gwangju 61186, Republic of Korea., Jung S; Division of Animal Science, College of Agriculture and Life Sciences, Chonnam National University, Gwangju 61186, Republic of Korea., Jung H; Animal Nutrition and Physiology Division, National Institute of Animal Science, Wanju 55365, Republic of Korea. |
| Abstrakt: |
Mycotoxin-contaminated feed or food can affect physiological responses and cause illnesses in humans and animals. In this study, we evaluated the effects of deoxynivalenol (DON) toxicity on the growth performance, blood biochemistry, histology, microbiome, and metabolism of rats fed with different toxin concentrations. After 1 week of acclimatization, seven-week-old male rats received 0.9% saline as a control, 0.02 mg/kg DON as T1, and 0.2 mg/kg DON as T2 via oral gavage for 4 weeks. The final body weight of the T2 group was significantly lower than that of the control and T1; however, the average daily gain, feed intake, and feed conversion ratio did not differ. Fibrosis and apoptosis were observed in various tissues as DON concentration increased. Creatinine and alkaline phosphatase levels were significantly lower in the DON-treated group than in the control. Firmicutes and Desulfobacterota phyla dominated the cecum, whereas those in the feces were Proteobacteria and Bacteroidetes. Metabolomic profiling showed phenylalanine, tyrosine, and tryptophan biosynthesis as the most prominent pathways. Overall, our results suggest that low-dose and short-term DON exposure can trigger several adverse effects in rats. Dietary toxicants in rats may explain the physiological effects associated with the metabolism commonly reported in animals. |
