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Effect of Compound Probiotics and Mycotoxin Degradation Enzymes on Alleviating Cytotoxicity of Swine Jejunal Epithelial Cells Induced by Aflatoxin B 1 and Zearalenone

机译:复合益生菌和霉菌毒素降解酶对黄曲霉毒素B 1和玉米赤霉烯酮诱导的猪空肠上皮细胞细胞毒性的减轻

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Zearalenone (ZEA) and aflatoxin B 1 (AFB 1 ) are two main kinds of mycotoxins widely existing in grain and animal feed that cause a lot of economic loss and health problems for animals and humans. In order to alleviate the cytotoxic effects of AFB 1 and ZEA on swine jejunal epithelial cells (IPEC-J2), the combination of a cell-free supernatant of compound probiotics (CFSCP) with mycotoxin degradation enzymes (MDEs) from Aspergillus oryzae was tested. The results demonstrated that coexistence of AFB 1 and ZEA had synergetic toxic effects on cell viability. The cell viability was decreased with mycotoxin concentrations increasing, but increased with incubation time extension. The necrotic cell rates were increased when 40 μg/L AFB 1 and/or 500 μg/L ZEA were added, but the addition of CFSCP + MDE suppressed the necrotic effects of AFB 1 + ZEA. The viable cell rates were decreased when AFB 1 and/or ZEA were added: However, the addition of CFSCP + MDE recovered them. The relative mRNA abundances of Bcl-2 , occludin , and ZO-1 genes were significantly upregulated, while Bax , caspase-3 , GLUT2 , ASCT2 , PepT1 , and IL6 genes were significantly downregulated by CFSCP + MDE addition, compared to the groups containing 40 μg/L AFB 1 and 500 μg/L ZEA. This research provided an effective strategy in alleviating mycotoxin cytotoxicity and keeping normal intestinal cell structure and animal health.
机译:玉米赤霉烯酮(ZEA)和黄曲霉毒素B 1(AFB 1)是谷物和动物饲料中广泛存在的两种主要霉菌毒素,它们对动物和人类造成许多经济损失和健康问题。为了减轻AFB 1和ZEA对猪空肠上皮细胞(IPEC-J2)的细胞毒性作用,测试了复合益生菌的无细胞上清液(CFSCP)与米曲霉的霉菌毒素降解酶(MDE)的组合。结果表明,AFB 1和ZEA的共存对细胞活力具有协同毒性作用。细胞活性随着霉菌毒素浓度的增加而降低,但随着孵育时间的延长而增加。当添加40μg/ L AFB 1和/或500μg/ L ZEA时,坏死细胞率增加,但是CFSCP + MDE的添加抑制了AFB 1 + ZEA的坏死作用。当添加AFB 1和/或ZEA时,活细胞率降低:但是,添加CFSCP + MDE可以恢复它们。与含CSCP的组相比,Bcl-2,occludin和ZO-1基因的相对mRNA丰度显着上调,而CFx + MDE的添加显着下调了Bax,caspase-3,GLUT2,ASCT2,PepT1和IL6基因。 40μg/ L AFB 1和500μg/ L ZEA。该研究为减轻霉菌毒素的细胞毒性,保持肠道细胞的正常结构和动物健康提供了有效的策略。

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