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二萜糖苷白术内酯的生物化学与毒理学

Biochemistry and toxicology of the diterpenoid glycoside atractyloside.

作者信息

Obatomi D K, Bach P H

机构信息

Department of Biochemistry, University of Jos, Nigeria.

出版信息

Food Chem Toxicol. 1998 Apr;36(4):335-46. doi: 10.1016/s0278-6915(98)00002-7.

Abstract

Atractyloside (Atr) is a diterpenoid glycoside that occurs naturally in plants (many of which are used in ethnomedicines) found in Europe, Africa, South America, Asia and the far East. It is also present in animal grazing forage. Atr (and its analogues) may be present at levels as high as 600 mg/kg dried plant material. Consumption of the plants containing Atr or carboxyatractyloside (carboxyAtr) has caused fatal renal proximal tubule necrosis and/or centrilobular hepatic necrosis in man and farm animals. Although pure Atr and crude plant extracts disrupt carbohydrate homeostasis and induce similar pathophysiological lesions in the kidney and liver, it is also possible that the toxicity of Atr may be confounded by the presence of other natural constituents in plants. Atr competitively inhibits the adenine nucleoside carrier in isolated mitochondria and thus blocks oxidative phosphorylation. This has been assumed to explain changes in carbohydrate metabolism and the toxic effects in liver and kidney. Although the acute toxicity of Atr is well described, many aspects of Atr toxicity (subchronic and chronic toxicity, reproductive toxicity, mutagenicity and carcinogenicity) have not been investigated and pharmacokinetic and metabolism data are limited. In vitro proximal tubular cells are selectively sensitive to Atr, whereas other renal cell types are quite resistant. There are also differences in the response of liver and renal tissue to Atr. Thus, not all of the clinical, biochemical and morphological changes caused by Atr can simply be explained on the basis of inhibition of mitochondrial phosphorylation. The relevance to a wider human risk is shown by the presence of Atr analogues in dried roasted Coffea arabica beans (17.5 32 mg/kg). There are no data to help identify the risk of low dose chronic exposure in human coffee consumers, nor is there information on the levels of Atr or its analogues in other commonly consumed human foodstuffs.

摘要

苍术苷(Atr)是一种二萜糖苷,天然存在于欧洲、非洲、南美洲、亚洲和远东地区的植物中(其中许多植物被用于民族医药)。它也存在于动物食用的草料中。Atr(及其类似物)在干燥植物材料中的含量可能高达600毫克/千克。食用含有Atr或羧基苍术苷(carboxyAtr)的植物已导致人类和农场动物发生致命的肾近端小管坏死和/或小叶中心性肝坏死。尽管纯Atr和粗植物提取物会破坏碳水化合物稳态,并在肾脏和肝脏中诱发类似的病理生理损伤,但Atr的毒性也可能因植物中其他天然成分的存在而受到混淆。Atr在离体线粒体中竞争性抑制腺嘌呤核苷载体,从而阻断氧化磷酸化。这被认为可以解释碳水化合物代谢的变化以及对肝脏和肾脏的毒性作用。尽管Atr的急性毒性已有充分描述,但Atr毒性的许多方面(亚慢性和慢性毒性、生殖毒性、致突变性和致癌性)尚未得到研究,药代动力学和代谢数据也有限。体外近端小管细胞对Atr具有选择性敏感性,而其他肾细胞类型则具有相当的抗性。肝脏和肾脏组织对Atr的反应也存在差异。因此,并非所有由Atr引起的临床、生化和形态学变化都能简单地基于线粒体磷酸化的抑制来解释。干燥烘焙的阿拉伯咖啡豆中存在Atr类似物(17.5 - 32毫克/千克),这表明其与更广泛的人类风险相关。目前尚无数据帮助确定咖啡消费者低剂量长期接触的风险,也没有关于其他常见人类食品中Atr或其类似物含量的信息。

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