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通过在大鼠饮食中添加丁香酚来增强其肝脏中UDP-葡萄糖醛酸基转移酶、UDP-葡萄糖脱氢酶和谷胱甘肽S-转移酶的活性。

Enhancement of UDP-glucuronyltransferase, UDP-glucose dehydrogenase, and glutathione S-transferase activities in rat liver by dietary administration of eugenol.

作者信息

Yokota H, Hashimoto H, Motoya M, Yuasa A

机构信息

Department of Veterinary Biochemistry, School of Veterinary Medicine, Rakuno Gakuen University, Hokkaido, Japan.

出版信息

Biochem Pharmacol. 1988 Mar 1;37(5):799-802. doi: 10.1016/0006-2952(88)90164-5.

Abstract

Male Fisher rats were fed a diet ad lib. containing eugenol (4-allyl-2-methoxyphenol) to observe its effects on liver drug-detoxifying enzymes such as UDP-glucuronyltransferase (GT), UDP-glucose dehydrogenase (DH) and glutathione S-transferase (GST). Liver weights were not affected significantly by a diet containing 3% eugenol (w/w) for 13 weeks. The activities of GT of liver microsomes toward various xenobiotic substances such as 4-nitrophenol, 1-naphthol, 4-hydroxybiphenyl and 4-methylumbelliferone were enhanced by dietary administration of eugenol, but the activity of GT toward its endogenous substrate, bilirubin, was not changed. Dose-response relationships between the enhancement of GT activities toward these xenobiotics and the dose of eugenol were observed. The induced higher activities of GT toward these xenobiotics were maintained during 13 weeks of eugenol treatment. Similar results on DH and GST activities in the liver cytosol were obtained by dietary administration of eugenol, while no effect on cytochrome P-450 content in the liver microsomes from the rats fed the eugenol diet was observed during 13 weeks. These results suggest that the intracellular content of the active intermediates of various drugs or carcinogens would be reduced by this specific enhancement of drug-detoxifying enzymes in the liver of rats given a diet containing eugenol, as previously described for a diet containing 2(3)-tert-butyl-4-hydroxyanisole (BHA) [Y-N. Cha and H. S. Heine, Cancer Res. 42, 2609 (1982)].

摘要

对雄性Fisher大鼠随意喂食含丁香酚(4 - 烯丙基 - 2 - 甲氧基苯酚)的饲料,以观察其对肝脏药物解毒酶如尿苷二磷酸葡萄糖醛酸基转移酶(GT)、尿苷二磷酸葡萄糖脱氢酶(DH)和谷胱甘肽S - 转移酶(GST)的影响。含3%(w/w)丁香酚的饲料喂养13周,对肝脏重量无显著影响。通过饮食给予丁香酚可增强肝脏微粒体中GT对多种外源物质如4 - 硝基苯酚、1 - 萘酚、4 - 羟基联苯和4 - 甲基伞形酮的活性,但GT对其内源性底物胆红素的活性未改变。观察到GT对这些外源物质活性增强与丁香酚剂量之间的剂量 - 反应关系。在丁香酚处理的13周内,诱导产生的GT对这些外源物质的较高活性得以维持。通过饮食给予丁香酚,在肝脏胞液中对DH和GST活性也得到了类似结果,而在13周内,观察到给丁香酚饲料喂养的大鼠肝脏微粒体中细胞色素P - 450含量无影响。这些结果表明,如先前对含2(3) - 叔丁基 - 4 - 羟基茴香醚(BHA)的饲料所描述的那样,给含丁香酚饲料喂养的大鼠肝脏中药物解毒酶的这种特异性增强会降低各种药物或致癌物活性中间体的细胞内含量[Y - N. Cha和H. S. Heine,《癌症研究》42, 2609 (1982)]。

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