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提高癌症化学保护多酚的代谢稳定性。

Improving metabolic stability of cancer chemoprotective polyphenols.

作者信息

Walle Thomas, Wen Xia, Walle U Kristina

机构信息

Medical University of South Carolina, Department of Cell and Molecular Pharmacology and Experimental Therapeutics, 173 Ashley Avenue, Charleston, SC 29425, USA.

出版信息

Expert Opin Drug Metab Toxicol. 2007 Jun;3(3):379-88. doi: 10.1517/17425255.3.3.379.

Abstract

Dietary flavonoids and other polyphenols have the potential to be developed as effective food supplements as well as drugs for the prevention, as well as treatment of, cancer and other disease conditions. However, their very poor oral bioavailability, mainly due to extensive conjugation by glucuronidation and sulfation, is a severe limiting factor. First, this review shows the use of a simple, commercially available model system, the human hepatic S9 fraction, by which metabolic stability can be assessed effectively and accurately. Second, permethylation of the polyphenols effectively blocks the metabolic conjugation reactions, thereby dramatically increasing both metabolic stability and intestinal absorption, while maintaining or even increasing the biologic activities. Thus, permethylated polyphenols may have a future as chemoprotective agents.

摘要

膳食类黄酮和其他多酚类物质有潜力被开发成为有效的食品补充剂以及用于预防和治疗癌症及其他疾病的药物。然而,它们极低的口服生物利用度,主要是由于通过葡萄糖醛酸化和硫酸化进行的广泛结合作用,是一个严重的限制因素。首先,本综述展示了使用一种简单的、市售的模型系统——人肝S9组分,通过该系统可以有效且准确地评估代谢稳定性。其次,多酚类物质的全甲基化有效地阻断了代谢结合反应,从而显著提高了代谢稳定性和肠道吸收,同时维持甚至增强了生物活性。因此,全甲基化多酚类物质可能有望成为化学预防剂。

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