G. J. Friedman Diabetes Institute and Division of Endocrinology, Department of Medicine, Beth Israel Medical Center, Albert Einstein College of Medicine, New York, USA.
Horm Metab Res. 2010 Sep;42(10):754-7. doi: 10.1055/s-0030-1262837. Epub 2010 Aug 13.
Vitamin D Receptor (VDR) is expressed in both animal and human ovarian tissue, however, the role of vitamin D in human ovarian steroidogenesis is unknown. Cultured human ovarian cells were incubated in tissue culture medium supplemented with appropriate substrates, with or without 50 pM-150 pM or 50 nM-150 nM of 1,25-(OH)2D3, and in the presence or absence of insulin. Progesterone, testosterone, estrone, estradiol, and IGFBP-1 concentrations in conditioned tissue culture medium were measured. Vitamin D receptor was present in human ovarian cells. 1,25-(OH)2D3 stimulated progesterone production by 13% (p<0.001), estradiol production by 9% (p<0.02), and estrone production by 21% (p<0.002). Insulin and 1,25-(OH)2D3 acted synergistically to increase estradiol production by 60% (p<0.005). 1,25-(OH)2D3 alone stimulated IGFBP-1 production by 24% (p<0.001), however, in the presence of insulin, 1,25-(OH)2D3 enhanced insulin-induced inhibition of IGFBP-1 production by 13% (p<0.009). Vitamin D stimulates ovarian steroidogenesis and IGFBP-1 production in human ovarian cells likely acting via vitamin D receptor. Insulin and vitamin D synergistically stimulate estradiol production. Vitamin D also enhances inhibitory effect of insulin on IGFBP-1 production.
维生素 D 受体(VDR)在动物和人类卵巢组织中均有表达,然而,维生素 D 在人类卵巢甾体生成中的作用尚不清楚。将培养的人类卵巢细胞在补充有适当底物的组织培养培养基中孵育,有或没有 50 pM-150 pM 或 50 nM-150 nM 的 1,25-(OH)2D3,并在有或没有胰岛素的情况下孵育。测量条件培养基中孕酮、睾酮、雌酮、雌二醇和 IGFBP-1 的浓度。维生素 D 受体存在于人类卵巢细胞中。1,25-(OH)2D3 使孕酮的产生增加了 13%(p<0.001),使雌二醇的产生增加了 9%(p<0.02),使雌酮的产生增加了 21%(p<0.002)。胰岛素和 1,25-(OH)2D3 协同作用使雌二醇的产生增加了 60%(p<0.005)。1,25-(OH)2D3 单独使 IGFBP-1 的产生增加了 24%(p<0.001),然而,在胰岛素存在的情况下,1,25-(OH)2D3 增强了胰岛素诱导的 IGFBP-1 产生的抑制作用 13%(p<0.009)。维生素 D 可能通过维生素 D 受体刺激人类卵巢细胞的卵巢甾体生成和 IGFBP-1 产生。胰岛素和维生素 D 协同刺激雌二醇的产生。维生素 D 还增强了胰岛素对 IGFBP-1 产生的抑制作用。