首页> 外文期刊>Turkish Journal of Veterinary and Animal Sciences >Ochratoxin A-induced serum biochemical alterations in New Zealand white rabbits (Oryctolagus cuniculus)
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Ochratoxin A-induced serum biochemical alterations in New Zealand white rabbits (Oryctolagus cuniculus)

机译:ch曲毒素A诱导的新西兰白兔(Oryctolagus cuniculus)血清生化变化

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Our objective was to study the effects of oral ochratoxin A (OT-A) intoxication in rabbits. New Zealand white rabbits of 8 weeks age, weighing 350-400 g, were utilized for the study. Rabbits were allotted randomly to 3 groups. Group 1 (6 animals) served as control. Groups 2 and 3 (12 animals each) were fed diets supplemented with 1000 and 2000 ppb OT-A, respectively, for 8 weeks. Blood samples were collected at weekly intervals from day 0 up to week 8 and sera were separated for biochemical analysis. Serum glucose and chloride levels showed marked progressive decrease whereas a marginal decrease was noticed in total protein and albumin. Serum levels of creatinine, and urea, and activities of aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase enzymes were increased in OT-A given groups. The effects were dose dependent. Globulins and albumin:globulin ratio was not affected significantly. SDS-PAGE revealed noticeable decrease in 81, 55-66, 48, and 44.5 KDa protein bands. Absence of 52 KDa proteins in the serum of rabbits fed 2000 ppb OT-A diets was noted. In conclusion, the observation of predominant serum biochemical alterations caused by 1000 and 2000 ppb OT-A in time and dose related fashion suggested progressive nephrotoxic and hepatotoxic effects in rabbits.
机译:我们的目的是研究口服曲毒素A(OT-A)中毒对兔子的影响。使用8周龄的新西兰白兔,体重350-400g,进行研究。将兔子随机分为3组。第1组(6只动物)用作对照。第2组和第3组(每组12只动物)分别饲喂补充有1000 ppb和2000 ppb OT-A的日粮,持续8周。从第0天到第8周,每周采集一次血样,并分离血清进行生化分析。血清葡萄糖和氯化物水平显示出明显的进行性下降,而总蛋白和白蛋白则有少量下降。 OT-A给予组的血清肌酐和尿素水平以及天冬氨酸转氨酶,丙氨酸转氨酶和碱性磷酸酶的活性增加。影响是剂量依赖性的。球蛋白和白蛋白:球蛋白比例未受到明显影响。 SDS-PAGE显示81、55-66、48和44.5 KDa蛋白条带明显减少。观察到饲喂2000 ppb OT-A日粮的兔血清中没有52 KDa蛋白。总之,以时间和剂量相关的方式观察到由1000和2000 ppb OT-A引起的主要血清生化改变,表明对兔具有逐步的肾毒性和肝毒性作用。

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