Dean Matthew, Murphy Brian T, Burdette Joanna E
Department of Medicinal Chemistry and Pharmacognosy, Center for Biomolecular Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.
Department of Medicinal Chemistry and Pharmacognosy, Center for Biomolecular Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.
Mol Cell Endocrinol. 2017 Feb 15;442:98-105. doi: 10.1016/j.mce.2016.12.013. Epub 2016 Dec 13.
Foods and botanical supplements can interfere with the endocrine system through the presence of phytosteroids - chemicals that interact with steroids receptors. Phytoestrogens are well studied, but compounds such as kaempferol, apigenin, genistein, ginsenoside Rf, and glycyrrhetinic acid have been shown to interact with non-estrogen nuclear receptors. These compounds can have agonist, antagonist, or mixed agonist/antagonist activity depending on compound, receptor, cell line or tissue, and concentration. Some phytosteroids have also been shown to inhibit steroid metabolizing enzymes, resulting in biological effects through altered endogenous steroid concentrations. An interesting example, compound A (4-[1-chloro-2-(methylamino)ethyl]phenyl acetate hydrochloride (1:1)) is a promising selective glucocorticoid receptor modulator (SGRM) based on a phytosteroid isolated from Salsola tuberculatiformis Botschantzev. Given that $6.9 billion of herbal supplements are sold each year, is clear that further identification and characterization of phytosteroids is needed to ensure the safe and effective use of botanical supplements.
食物和植物性补充剂中的植物甾醇(与类固醇受体相互作用的化学物质)会干扰内分泌系统。植物雌激素已得到充分研究,但诸如山奈酚、芹菜素、染料木黄酮、人参皂苷Rf和甘草次酸等化合物已被证明可与非雌激素核受体相互作用。根据化合物、受体、细胞系或组织以及浓度的不同,这些化合物可能具有激动剂、拮抗剂或混合激动剂/拮抗剂活性。一些植物甾醇还被证明可抑制类固醇代谢酶,通过改变内源性类固醇浓度产生生物学效应。一个有趣的例子是,化合物A(4-[1-氯-2-(甲氨基)乙基]苯基乙酸盐酸盐(1:1))是一种有前景的选择性糖皮质激素受体调节剂(SGRM),它基于从瘤果猪毛菜中分离出的一种植物甾醇。鉴于每年草药补充剂的销售额达69亿美元,显然需要进一步鉴定和表征植物甾醇,以确保植物性补充剂的安全有效使用。