Swart Amanda C, Johannes Inge D, Sathyapalan Thozhukat, Atkin Stephen L
Department of Biochemistry, Stellenbosch University, Stellenbosch, South Africa.
Academic Diabetes, Endocrinology and Metabolism, University of Hull, Hull, United Kingdom.
Front Endocrinol (Lausanne). 2019 Apr 11;10:229. doi: 10.3389/fendo.2019.00229. eCollection 2019.
This study is a analysis of steroid hormones before and after administration of pharmacological doses of soy isoflavones in a large cohort of men and women from two independent studies. Isoflavones are reported to inhibit mineralo- and glucocorticoid hormone production as well as reproductive steroids and . We focused on cytochrome P450 17α-hydroxylase (CYP17A1) which catalyses the production of dehydroepiandrosterone (DHEA), in the androgen biosynthesis pathway to elucidate effects on sex steroids . Effects of soy isoflavones on steroid levels in two studies comprising 400 patients were examined: 200 men (study 1; 3 months duration) and 200 postmenopausal women (study 2; 6 months duration), randomized to consume 15 g soy protein with 66 mg isoflavones (SPI) or 15 g soy protein alone without isoflavones (SP) daily. Effects of genistein and daidzein on steroid metabolism were determined , in HEK293 cells expressing CYP17A1 and in the human adrenocortical carcinoma H295R cell model. SPI decreased serum dehydroepiandrosterone sulfate (DHEAS) levels in both men and women ( < 0.01), with decreased androstenedione (A4) ( < 0.01) in women not observed in men ( < 0.86). Cortisol, cortisone, 11-deoxycortisol, aldosterone, testosterone (T), or estradiol (E2) levels were unchanged. The dual hydroxylase and lyase activity of CYP17A1, which catalyses the biosynthesis of androgen precursors, and 3β-hydroxysteroid dehydrogenase (3βHSD2) were investigated . In transiently transfected HEK293 cells, only the lyase activity was inhibited by both genistein, 20% ( < 0.001) and daidzein, 58% ( < 0.0001). In forskolin-stimulated H295R cells DHEA production was decreased by daidzein ( < 0.05) and genistein, confirming inhibition of the lyase activity by the isoflavones. clinical data suggested inhibition of CYP17A1 17,20 lyase within the adrenal in men and within the ovary and adrenal in females. This was confirmed with inhibition of the lyase activity by both genistein and daidzein. In addition, 3βHSD2 was inhibited perhaps accounting for decreased A4 levels observed in females. The decreased DHEAS and A4 levels together with the inhibition of the 17,20 lyase activity of CYP17A1, may impact production of androgens in clinical conditions associated with androgen excess. ISRCTN number: ISRCTN55827330 ISRCTN number: ISRCTN 90604927.
本研究对两项独立研究中大量男性和女性服用药理剂量大豆异黄酮前后的甾体激素进行了分析。据报道,异黄酮可抑制盐皮质激素和糖皮质激素的产生以及生殖甾体激素。我们重点研究了细胞色素P450 17α-羟化酶(CYP17A1),其在雄激素生物合成途径中催化脱氢表雄酮(DHEA)的产生,以阐明对性甾体激素的影响。在两项共包含400名患者的研究中,检测了大豆异黄酮对甾体激素水平的影响:200名男性(研究1;为期3个月)和200名绝经后女性(研究2;为期6个月),随机分组,分别每日食用含66毫克异黄酮的15克大豆蛋白(SPI)或不含异黄酮的15克大豆蛋白(SP)。在表达CYP17A1的HEK293细胞和人肾上腺皮质癌H295R细胞模型中,测定了染料木黄酮和大豆苷元对甾体代谢的影响。SPI降低了男性和女性血清硫酸脱氢表雄酮(DHEAS)水平(P<0.01),女性雄烯二酮(A4)水平降低(P<0.01),而男性未观察到该现象(P>0.86)。皮质醇、可的松、11-脱氧皮质醇、醛固酮、睾酮(T)或雌二醇(E2)水平未发生变化。研究了催化雄激素前体生物合成的CYP17A1的双羟化酶和裂解酶活性以及3β-羟类固醇脱氢酶(3βHSD2)。在瞬时转染的HEK293细胞中,染料木黄酮(20%,P<0.001)和大豆苷元(58%,P<0.0001)均抑制了裂解酶活性。在福斯高林刺激的H295R细胞中,大豆苷元和染料木黄酮均降低了DHEA的产生,证实异黄酮对裂解酶活性有抑制作用。临床数据表明,男性肾上腺内以及女性卵巢和肾上腺内的CYP17A1 17,20-裂解酶受到抑制。染料木黄酮和大豆苷元对裂解酶活性的抑制作用证实了这一点。此外,3βHSD2可能受到抑制,这或许可以解释女性中观察到的A4水平降低。DHEAS和A4水平的降低以及CYP17A1的17,20-裂解酶活性受到抑制,可能会影响与雄激素过多相关临床情况下雄激素的产生。国际标准随机对照试验编号:ISRCTN55827330 国际标准随机对照试验编号:ISRCTN 90604927。