Meijs-Roelofs H M, Kramer P, Gribling-Hegge L
J Endocrinol. 1982 Jan;92(1):37-42. doi: 10.1677/joe.0.0920037.
A possible role of 5 alpha-androstane-3 alpha, 17 beta-diol (3 alpha-androstanediol) in the control of FSH secretion was studied at various ages in ovariectomized rats. In the rat strain used, vaginal opening, coincident with first ovulation, generally occurs between 37 and 42 days of age. If 3 alpha-androstanediol alone was given as an ovarian substitute, an inhibitory effect on FSH release was evident with all three doses tested (50, 100, 300 microgram/100 g body wt) between 13 and 30 days of age; at 33-35 days of age only the 300 microgram dose caused some inhibition of FSH release. Results were more complex if 3 alpha-androstanediol was given in combined treatment with oestradiol and progesterone. Given with progesterone, 3 alpha-androstanediol showed a synergistic inhibitory action on FSH release between 20 and 30 days of age. However, when 3 alpha-androstanediol was combined with oestradiol a clear decrease in effect, as compared to the effect of oestradiol alone, was found between 20 and 30 days of age. Also the effect of combined oestradiol and progesterone treatment was greater than the effect of combined treatment with oestradiol, progesterone and 3 alpha-androstanediol. At all ages after day 20 none of the steroid combinations tested was capable of maintaining FSH levels in ovariectomized rats similar to those in intact rats. It is concluded that 3 alpha-androstanediol might play a role in the control of FSH secretion in the immature rat, but after day 20 the potentially inhibitory action of 3 alpha androstanediol on FSH secretion is limited in the presence of oestradiol.
在去卵巢大鼠的不同年龄段,研究了5α-雄甾烷-3α,17β-二醇(3α-雄甾二醇)在促卵泡激素(FSH)分泌调控中的可能作用。在所使用的大鼠品系中,与首次排卵同时发生的阴道开口通常出现在37至42日龄之间。如果单独给予3α-雄甾二醇作为卵巢替代物,在13至30日龄时,所测试的所有三种剂量(50、100、300微克/100克体重)对FSH释放均有明显的抑制作用;在33 - 35日龄时,只有300微克剂量对FSH释放有一定抑制作用。如果3α-雄甾二醇与雌二醇和孕酮联合使用,结果会更复杂。与孕酮联合使用时,3α-雄甾二醇在20至30日龄之间对FSH释放表现出协同抑制作用。然而,当3α-雄甾二醇与雌二醇联合使用时,在20至30日龄之间,与单独使用雌二醇的效果相比,作用明显减弱。同时,雌二醇和孕酮联合治疗的效果也大于雌二醇、孕酮和3α-雄甾二醇联合治疗的效果。在20日龄后的所有年龄段,所测试的任何类固醇组合都无法使去卵巢大鼠的FSH水平维持在与完整大鼠相似的水平。结论是,3α-雄甾二醇可能在未成熟大鼠的FSH分泌调控中发挥作用,但在20日龄后,在有雌二醇存在的情况下,3α-雄甾二醇对FSH分泌的潜在抑制作用受到限制。