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栀子苷对大鼠肝脏细胞色素P-450依赖性单加氧酶、谷胱甘肽及谷胱甘肽S-转移酶的调节作用

Modulation of cytochrome P-450-dependent monooxygenases, glutathione and glutathione S-transferase in rat liver by geniposide from Gardenia jasminoides.

作者信息

Kang J J, Wang H W, Liu T Y, Chen Y C, Ueng T H

机构信息

Institute of Toxicology, College of Medicine, National Taiwan University, Taipei, Taiwan, ROC.

出版信息

Food Chem Toxicol. 1997 Oct-Nov;35(10-11):957-65. doi: 10.1016/s0278-6915(97)87265-1.

Abstract

Geniposide is an iridoid glycoside extracted from the fruits of Gardenia jasminoides, which are used as a food colorant and as a traditional Chinese medicine for treatment of hepatic and inflammatory diseases. The effects of geniposide and G. jasminoides fruit crude extract on liver cytochrome P-450 (P-450)-dependent monooxygenases, glutathione and glutathione S-transferase were investigated using rats treated orally with the iridoid glycoside (0.1 g/kg body weight/day) or the fruit crude extract (2 g/kg/day) for 4 days. The treatments decreased serum urea nitrogen level but increased liver to body weight ratio, total hepatic glutathione content and hepatic cytosolic glutathione S-transferase activity. Treatments with geniposide and G. jasminoides decreased P-450 content, benzo[a]pyrene hydroxylation, 7-ethoxycoumarin O-deethylation, and erythromycin N-demethylation activities in liver microsomes without affecting aniline hydroxylation activity. The natural products had no effect on glutathione content and monooxygenase activities in kidney microsomes. Immunoblotting analyses of liver microsomal proteins using mouse monoclonal antibody 2-13-1 to rat P4503A1/2 revealed that geniposide and G. jasminoides crude extract decreased the intensity of a P4503A-immunorelated protein. Protein blots probed with mouse monoclonal antibody 1-12-3 to rat P4501A1 and rabbit polyclonal antibody against human P4502E1 showed that both treatments had little or no effect on P4501A and 2E proteins. The present findings demonstrate that geniposide from G. jasminoides has the ability to inhibit a P4503A monooxygenase and increase glutathione content in rat liver.

摘要

栀子苷是从栀子果实中提取的一种环烯醚萜苷,栀子果实被用作食用色素和治疗肝脏及炎症性疾病的传统中药。采用大鼠口服环烯醚萜苷(0.1克/千克体重/天)或果实粗提物(2克/千克/天)4天的方法,研究了栀子苷和栀子果实粗提物对肝脏细胞色素P-450(P-450)依赖性单加氧酶、谷胱甘肽及谷胱甘肽S-转移酶的影响。这些处理降低了血清尿素氮水平,但增加了肝体比、肝脏总谷胱甘肽含量及肝脏胞质谷胱甘肽S-转移酶活性。栀子苷和栀子处理降低了肝微粒体中P-450含量、苯并[a]芘羟化、7-乙氧基香豆素O-脱乙基及红霉素N-脱甲基活性,而不影响苯胺羟化活性。这些天然产物对肾微粒体中的谷胱甘肽含量及单加氧酶活性没有影响。使用针对大鼠P4503A1/2的小鼠单克隆抗体2-13-1对肝微粒体蛋白进行免疫印迹分析显示,栀子苷和栀子粗提物降低了P4503A免疫相关蛋白的强度。用针对大鼠P4501A1的小鼠单克隆抗体1-12-3及针对人P4502E1的兔多克隆抗体进行蛋白印迹检测表明,两种处理对P4501A和2E蛋白几乎没有影响或没有影响。目前的研究结果表明,栀子中的栀子苷具有抑制大鼠肝脏中P4503A单加氧酶并增加谷胱甘肽含量的能力。

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