Dekanski J B
Br J Pharmacol. 1980;71(1):11-6. doi: 10.1111/j.1476-5381.1980.tb10903.x.
1 Endocrine and anti-fertility studies were carried out on a fluorinated bibenzyl, bifluranol, in rats and mice. 2 A potent anti-prostatic activity of bifluranol was shown to be comparable to diethylstilboestrol (DES). In contrast, its oestrogenic potency by the oral route was about eight times less than that of DES. 3 In comparative short and long-term anti-androgenic and fertility studies in rats and in studies on sexual potency and reproductive performance in male mice, bifluranol given orally was shown to produce fully reversible suppression of accessory sexual structures without impairment of spermatogenesis and fertility. In contrast, DES administered in the same dose reduced spermatogenesis as well as accessory sexual glands. 4 Bifluranol lowered serum luteinising hormone (LH) levels without affecting follicle stimulating hormone (FSH). Under similar conditions DES reduces both LH and FSH levels. Since bifluranol does not antagonize androgen-induced stimulation of the prostate in castrated rats, its anti-prostatic effect is interpreted as a negative, hormonostatic feedback activity, mediated through a selective inhibition of LH secretion.
对一种氟化联苄——双氟拉醇,在大鼠和小鼠身上进行了内分泌及抗生育研究。
双氟拉醇显示出强效的抗前列腺活性,可与己烯雌酚(DES)相媲美。相比之下,其经口服途径的雌激素活性约为DES的八分之一。
在大鼠的短期和长期抗雄激素及生育研究以及雄性小鼠的性功能和生殖性能研究中,口服双氟拉醇被证明能完全可逆地抑制附属性器官结构,而不损害精子发生和生育能力。相比之下,给予相同剂量的DES会降低精子发生以及附属性腺。
双氟拉醇降低血清促黄体生成素(LH)水平,而不影响促卵泡生成素(FSH)。在类似条件下,DES会降低LH和FSH水平。由于双氟拉醇不会拮抗去势大鼠中雄激素诱导的前列腺刺激,其抗前列腺作用被解释为一种通过选择性抑制LH分泌介导的负性、激素稳态反馈活性。