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在亚慢性膳食暴露于黄曲霉毒素B1期间猪肝中药物代谢酶的选择性损伤

Selective impairment of drug-metabolizing enzymes in pig liver during subchronic dietary exposure to aflatoxin B1.

作者信息

Meissonnier Guylaine M, Laffitte Joelle, Loiseau Nicolas, Benoit Etienne, Raymond Isabelle, Pinton Philippe, Cossalter Anne-Marie, Bertin Gérard, Oswald Isabelle P, Galtier Pierre

机构信息

Laboratoire de Pharmacologie-Toxicologie UR66, INRA, F-31931 Toulouse Cedex 9, France.

出版信息

Food Chem Toxicol. 2007 Nov;45(11):2145-54. doi: 10.1016/j.fct.2007.05.012. Epub 2007 Jun 2.

Abstract

Consequences of subchronic exposure to aflatoxin B1 (AFB1) on liver monooxygenase and transferase enzymes were compared in control pigs and pigs given 385, 867 or 1,807 microg AFB1/kg of feed for 4 weeks. Animals exposed to the highest dose of toxin developed clinical signs of aflatoxicosis, like liver fibrosis, hepatic dysfunction and decreased weight gain. This group had significantly lower levels of liver cytochrome P450, ethoxyresorufin O-deethylase (EROD) activity, testosterone metabolism, P450 1A and P450 3A protein expression. By comparison, mild degenerative hepatic changes, no hepatic dysfunction but a similar pattern of liver P450 enzymes activity without changes in P450 3A expression were observed in pigs exposed to 867 microg AFB1/kg of feed. Benzphetamine and aminopyrine N-demethylase activities were increased in pigs exposed to 867 or 1,807microg AFB1/kg of feed. Pigs exposed to 385 microg AFB1/kg of feed had low levels of EROD activity and all other biotransformation and clinical parameters remained at control levels. Aniline hydroxylase activity, P450 2C protein expression, UDP-glucuronosyl and glutathione S-transferase activities were unaffected at all doses of AFB1. In conclusion, P450 1A and P450 3A appear to be specific targets of AFB1 even if pig did not display clinical sign of liver toxicosis.

摘要

在对照猪和喂食含385、867或1807微克黄曲霉毒素B1(AFB1)/千克饲料4周的猪中,比较了亚慢性暴露于AFB1对肝脏单加氧酶和转移酶的影响。暴露于最高剂量毒素的动物出现了黄曲霉毒素中毒的临床症状,如肝纤维化、肝功能障碍和体重增加减少。该组肝脏细胞色素P450、乙氧异吩恶唑酮O-脱乙基酶(EROD)活性、睾酮代谢、P450 1A和P450 3A蛋白表达水平显著降低。相比之下,在喂食867微克AFB1/千克饲料的猪中,观察到轻度的肝脏退行性变化,无肝功能障碍,但肝脏P450酶活性模式相似,P450 3A表达无变化。暴露于867或1807微克AFB1/千克饲料的猪中,苄非他明和氨基比林N-脱甲基酶活性增加。暴露于385微克AFB1/千克饲料的猪EROD活性水平较低,所有其他生物转化和临床参数保持在对照水平。在所有AFB1剂量下,苯胺羟化酶活性、P450 2C蛋白表达、UDP-葡萄糖醛酸基转移酶和谷胱甘肽S-转移酶活性均未受影响。总之,即使猪未表现出肝脏中毒的临床症状,P450 1A和P450 3A似乎也是AFB1的特定靶点。

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