Ronis Martin J J
a Department of Pharmacology & Experimental Therapeutics , Louisiana State University Health Sciences Center , New Orleans , LA , USA.
Drug Metab Rev. 2016 Aug;48(3):331-41. doi: 10.1080/03602532.2016.1206562. Epub 2016 Jul 20.
Cytochromes P450 (CYPs) play an important role in metabolism and clearance of most clinically utilized drugs and other xenobiotics. They are important in metabolism of endogenous compounds including fatty acids, sterols, steroids and lipid-soluble vitamins. Dietary factors such as phytochemicals are capable of affecting CYP expression and activity, which may be important in diet-drug interactions and in the development of fatty liver disease, cardiovascular disease and cancer. One important diet-CYP interaction is with diets containing plant proteins, particularly soy protein. Soy diets are traditionally consumed in Asian countries and are linked to lower incidence of several cancers and of cardiovascular disease in Asian populations. Soy is also an important protein source in vegetarian and vegan diets and the sole protein source in soy infant formulas. Recent studies suggest that consumption of soy can inhibit induction of CY1 enzymes by polycyclic aromatic hydrocarbons (PAHs) which may contribute to cancer prevention. In addition, there are data to suggest that soy components promiscuously activate several nuclear receptors including PXR, PPAR and LXR resulting in increased expression of CYP3As, CYP4As and CYPs involved in metabolism of cholesterol to bile acids. Such soy-CYP interactions may alter drug pharmacokinetics and therapeutic efficacy and are associated with improved lipid homeostasis and reduced risk of cardiovascular disease. The current review summarizes results from in vitro; in vivo and clinical studies of soy-CYP interactions and examines the evidence linking the effects of soy diets on CYP expression to isoflavone phytoestrogens, particularly, genistein and daidzein that are associated with soy protein.
细胞色素P450(CYPs)在大多数临床使用药物及其他外源性物质的代谢和清除过程中发挥着重要作用。它们在内源性化合物(包括脂肪酸、固醇、类固醇和脂溶性维生素)的代谢中也很重要。植物化学物质等饮食因素能够影响CYPs的表达和活性,这在饮食与药物的相互作用以及脂肪肝疾病、心血管疾病和癌症的发展过程中可能具有重要意义。一种重要的饮食与CYPs的相互作用是与含有植物蛋白,特别是大豆蛋白的饮食之间的相互作用。在亚洲国家,传统上人们食用大豆饮食,并且亚洲人群中几种癌症和心血管疾病的发病率较低与大豆饮食有关。大豆也是素食和纯素饮食中的重要蛋白质来源,并且是大豆婴儿配方奶粉中的唯一蛋白质来源。最近的研究表明,食用大豆可以抑制多环芳烃(PAHs)对CY1酶的诱导作用,这可能有助于预防癌症。此外,有数据表明,大豆成分可广泛激活多种核受体,包括孕烷X受体(PXR)、过氧化物酶体增殖物激活受体(PPAR)和肝X受体(LXR),从而导致参与胆固醇代谢为胆汁酸的CYP3A、CYP4A和CYPs的表达增加。这种大豆与CYPs的相互作用可能会改变药物的药代动力学和治疗效果,并与改善脂质稳态及降低心血管疾病风险有关。本综述总结了大豆与CYPs相互作用的体外、体内及临床研究结果,并探讨了将大豆饮食对CYPs表达的影响与异黄酮植物雌激素(特别是与大豆蛋白相关的染料木黄酮和大豆苷元)联系起来的证据。