Kauppila A, Isomaa V, Rönnberg L, Vierikko P, Vihko R
Fertil Steril. 1985 Oct;44(4):466-70. doi: 10.1016/s0015-0282(16)48913-2.
The effects of gestrinone (R 2323) on endometrial and endometriosis tissue concentrations of cytosol estrogen and progestin receptors and the activity of 17 beta-hydroxysteroid dehydrogenase (17 beta-HSD) were investigated in 11 patients operated on because of suspected external endometriosis. Serum concentrations of luteinizing hormone, follicle-stimulating hormone, estradiol (E2), progesterone, testosterone (T), and sex-hormone-binding globulin (SHBG) were also investigated. After one control cycle, the patients received 2.5 mg of oral gestrinone twice weekly from the fifth day of the first treatment cycle until the eighth day of the second treatment cycle, the day of operation being day 10. Treatment with gestrinone decreased serum concentrations of T during the second treatment cycle and effected a major decrease in SHBG during both treatment cycles, resulting in highly increased free T and free E2 indices. The effects of gestrinone on the endometrium, a decrease in estrogen and progestin receptors, and induction of 17 beta-HSD are characteristic progestin actions. These parameters remained unchanged in endometriosis tissue. Our data indicate that gestrinone has effects that are typical of androgens and progestins in patients with endometriosis.
在11例因疑似外在性子宫内膜异位症而接受手术的患者中,研究了孕三烯酮(R 2323)对子宫内膜和子宫内膜异位症组织中胞质雌激素和孕激素受体浓度以及17β-羟类固醇脱氢酶(17β-HSD)活性的影响。还研究了血清促黄体生成素、促卵泡激素、雌二醇(E2)、孕酮、睾酮(T)和性激素结合球蛋白(SHBG)的浓度。在一个对照周期后,患者从第一个治疗周期的第5天开始,每周两次口服2.5mg孕三烯酮,直至第二个治疗周期的第8天,手术日为第10天。孕三烯酮治疗在第二个治疗周期降低了血清T浓度,并且在两个治疗周期均使SHBG大幅下降,导致游离T和游离E2指数大幅升高。孕三烯酮对子宫内膜的影响、雌激素和孕激素受体减少以及17β-HSD的诱导是典型的孕激素作用。这些参数在子宫内膜异位症组织中保持不变。我们的数据表明,孕三烯酮在子宫内膜异位症患者中具有雄激素和孕激素的典型作用。