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去甲二氢愈创木酸在克隆-9大鼠肝细胞培养物中的促氧化活性和毒性。

Prooxidant activity and toxicity of nordihydroguaiaretic acid in clone-9 rat hepatocyte cultures.

作者信息

Sahu Saura C, Ruggles Dennis I, O'Donnell Michael W

机构信息

Division of Toxicology, Office of Applied Research and Safety Assessment, Center for Food Safety and Applied Nutrition, US Food and Drug Administration, 8301 Muirkirk Road, Laurel, MD 20708, USA.

出版信息

Food Chem Toxicol. 2006 Oct;44(10):1751-7. doi: 10.1016/j.fct.2006.05.016. Epub 2006 Jun 7.

Abstract

Nordihydroguaiaretic acid (NDGA) is a polyphenol. It is present at high concentrations in the leaves of the evergreen desert shrub, Larrea tridentate (Creosote bush), which has a long history of medicinal use traditionally by the native Americans and Mexicans. It is generally believed that the antioxidant properties of NDGA are responsible for the medicinal value of this desert shrub. The clone-9 rat hepatocyte cultures were used as an in vitro model to assess the hepatotoxic potential of NDGA and to determine whether it exhibits any prooxidant activity. The hepatocyte cultures were treated with NDGA for 2 h at 37 degrees C at concentrations of 0-100 microM. After the treatment period the cells, the culture supernatants and cell lysates were assayed for evaluation of prooxidant activity and toxicity of NDGA. Oxidative stress level and oxidative cell injury as measured by the peroxidation of membrane lipids and DNA double-strand breaks were used to index prooxidant activity. Cytotoxicity as measured by the leakage of the liver enzyme lactate dehydrogenase (LDH) into the culture medium, mitochondrial function and extent of cell proliferation were used as the endpoints of toxicity. Significant concentration-dependent differences were observed in these biomarkers over the concentration range examined demonstrating the prooxidant activity and toxicity of NDGA in clone-9 rat hepatocyte cultures.

摘要

去甲二氢愈创木酸(NDGA)是一种多酚。它在常绿沙漠灌木三齿拉瑞阿(Larrea tridentate,又称牧豆树)的叶子中含量很高,美洲原住民和墨西哥人传统上使用这种植物治病已有很长历史。人们普遍认为,NDGA的抗氧化特性是这种沙漠灌木具有药用价值的原因。克隆9大鼠肝细胞培养物被用作体外模型,以评估NDGA的肝毒性潜力,并确定它是否具有任何促氧化活性。将肝细胞培养物在37摄氏度下用浓度为0 - 100微摩尔的NDGA处理2小时。处理期结束后,对细胞、培养上清液和细胞裂解物进行检测,以评估NDGA的促氧化活性和毒性。通过膜脂质过氧化和DNA双链断裂测量的氧化应激水平和氧化性细胞损伤被用作促氧化活性的指标。通过肝酶乳酸脱氢酶(LDH)泄漏到培养基中的情况、线粒体功能和细胞增殖程度来测量的细胞毒性被用作毒性终点。在所研究的浓度范围内,这些生物标志物存在显著的浓度依赖性差异,表明NDGA在克隆9大鼠肝细胞培养物中具有促氧化活性和毒性。

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