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长期暴露于黄曲霉毒素B1和黄曲霉毒素M1对黄曲霉毒素B1与肝脏大分子在体内共价结合的影响。

Effects of chronic exposure to aflatoxin B1 and aflatoxin M1 on the in vivo covalent binding of aflatoxin B1 to hepatic macromolecules.

作者信息

Loury D N, Hsieh D P

出版信息

J Toxicol Environ Health. 1984;13(4-6):575-87. doi: 10.1080/15287398409530522.

Abstract

Induction of resistance to aflatoxin B1 (AFB1) binding to cellular macromolecules in the rat by chronic exposure to AFB1 and aflatoxin M1 (AFM1) was investigated. The binding of [14C]AFB1 to liver macromolecules was measured in F-344 rats fed 0.5 ppb or 50 ppb AFM1 or 50 ppb AFB1 for 41 wk. The animals then received an intragastric dose of [14C]AFB1 at 5 micrograms/kg and were sacrificed 6 h later. Hepatic DNA, RNA, and protein were isolated by chloroform-phenol extraction and hydroxylapatite chromatography. In animals preexposed to 50 ppb AFB1, labeled AFB1 binding to DNA, RNA, and protein was decreased by 72%, 74%, and 61%, respectively. Preexposure to AFM1 resulted in a small reduction in binding to nucleic acids. Glutathione transferase activity was increased by 133% in animals fed 50 ppb AFB1, by 48% in those preexposed to 50 ppb AFM1, and remained at control values in rats fed 0.5 ppb AFM1. These results suggest that the induction of detoxification enzymes following chronic exposure to aflatoxin might contribute to the reduction in covalent binding of AFB1 to macromolecules.

摘要

研究了长期暴露于黄曲霉毒素B1(AFB1)和黄曲霉毒素M1(AFM1)对大鼠细胞大分子与AFB1结合抗性的诱导作用。在给F-344大鼠喂食0.5 ppb或50 ppb AFM1或50 ppb AFB1 41周后,测定[14C]AFB1与肝脏大分子的结合情况。然后给这些动物以5微克/千克的剂量灌胃[14C]AFB1,并在6小时后处死。通过氯仿-苯酚萃取和羟基磷灰石色谱法分离肝脏中的DNA、RNA和蛋白质。在预先暴露于50 ppb AFB1的动物中,标记的AFB1与DNA、RNA和蛋白质的结合分别减少了72%、74%和61%。预先暴露于AFM1导致与核酸的结合略有减少。喂食50 ppb AFB1的动物中谷胱甘肽转移酶活性增加了133%,预先暴露于50 ppb AFM1的动物中增加了48%,而喂食0.5 ppb AFM1的大鼠中该酶活性保持在对照值。这些结果表明,长期暴露于黄曲霉毒素后解毒酶的诱导可能有助于减少AFB1与大分子的共价结合。

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