Santell R C, Chang Y C, Nair M G, Helferich W G
Department of Food Science and Human Nutrition, Michigan State University, E. Lansing 48824, USA.
J Nutr. 1997 Feb;127(2):263-9. doi: 10.1093/jn/127.2.263.
These studies were undertaken to assess the estrogenic and antiestrogenic effects of dietary genistein. To determine estrogenic effects, genistein was mixed into a modified AIN-76 or AIN-93G semipurified diet at 0 (negative control), 150, 375 or 750 microg/g and 17, beta-estradiol at 1.0 microg/g and fed to ovariectomized 70-d-old Sprague-Dawley rats. Estrogenic potency was determined by analyzing uterine weight, mammary gland development, plasma prolactin and expression of uterine c-fos. Dietary genistein (375 and 750 microg/g) increased uterine wet and dry weights (P < 0.05). Mammary gland regression following ovariectomy was significantly inhibited by dietary genistein at 750 microg/g (P < 0.05). Plasma prolactin was significantly greater in ovariectomized rats fed genistein (750 microg/g) compared with comparable rats not receiving genistein. The relative binding affinity of genistein to the estrogen receptor (ER) was 0.01 that of estradiol. Genistein (750 microg/g) induced the uterine expression of c-fos. To evaluate potential antiestrogenic effects, genistein and estradiol were mixed into the modified AIN diets at the doses noted above and fed to ovariectomized rats. Dietary genistein (375 or 750 microg/g) did not inhibit the effects of estradiol on uterine weight, mammary gland development or plasma prolactin. Serum concentration of total genistein (conjugated plus free) in rats fed 750 microg/g was 2.2 micromol/L and free genistein was 0.4 micromol/L. Administration of dietary genistein at 750 microg/g can exert estrogenic effects in the uterus, mammary gland and hypothalamic/pituitary axis. Dietary genistein (750 microg/g) did not antagonize the action of estradiol in estradiol-supplemented ovariectomized rats or in intact rats.
开展这些研究以评估膳食染料木黄酮的雌激素和抗雌激素作用。为确定雌激素作用,将染料木黄酮以0(阴性对照)、150、375或750微克/克的剂量混入改良的AIN - 76或AIN - 93G半纯化日粮中,将17β - 雌二醇以1.0微克/克的剂量混入,然后喂给70日龄去卵巢的斯普拉格 - 道利大鼠。通过分析子宫重量、乳腺发育、血浆催乳素和子宫c - fos的表达来确定雌激素效力。膳食染料木黄酮(375和750微克/克)增加了子宫湿重和干重(P < 0.05)。750微克/克的膳食染料木黄酮显著抑制了去卵巢后的乳腺退化(P < 0.05)。与未接受染料木黄酮的对照大鼠相比,喂食染料木黄酮(750微克/克)的去卵巢大鼠血浆催乳素显著更高。染料木黄酮与雌激素受体(ER)的相对结合亲和力是雌二醇的0.01。染料木黄酮(750微克/克)诱导子宫c - fos的表达。为评估潜在的抗雌激素作用,将染料木黄酮和雌二醇以上述剂量混入改良的AIN日粮中喂给去卵巢大鼠。膳食染料木黄酮(375或750微克/克)并未抑制雌二醇对子宫重量、乳腺发育或血浆催乳素的作用。喂食750微克/克染料木黄酮的大鼠血清中总染料木黄酮(结合型加游离型)浓度为2.2微摩尔/升,游离染料木黄酮为0.4微摩尔/升。以750微克/克的剂量给予膳食染料木黄酮可在子宫、乳腺和下丘脑/垂体轴发挥雌激素作用。膳食染料木黄酮(750微克/克)在补充雌二醇的去卵巢大鼠或完整大鼠中并未拮抗雌二醇的作用。