Target sites for suppressing fertility in the male.

Advances in sex hormone research Pub Date : 1976-01-01
M R Prasad, M Rajalakshmi
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Abstract

The present status and perspectives in the control of fertility in the male have been reviewed. There are two potential sites in the male reproductive processes that can be used as targets for regulation of fertility in the male: (1) inhibition of spermatogenesis, and (2) interference with sperm maturation in the epididymis. A variety of compounds tested for their antispermatogenic action in laboratory animals have no future for the control of fertility in the human male because of a number of undesirable side effects (cf. Prasad, 1973). Progestational compounds inhibit spermatogenesis by affecting the hypothalamo-hypophysial system and result in impairment of libido. The possibility of adjustment of the minimal dose of progestational compounds required to induce suppression of spermatogenesis and reduction of plasma testosterone to a level compatible with the maintenance of normalcy of libido and potency needs to be studied. A new approach to contraception in the male involves the use of a combination of progestational compounds for suppression of spermatogenesis along with testosterone (administered through silastic capsule implants or as intramuscular injections) for maintenance of libido and accessory sex gland function. A number of such combinations have been tested clinically with some success. However, the limitations of side effects, such as weight gain, gynecomastia, and psychological complications preclude their long-term use for contraception in man. Short-term use of these combination regimens by the male for 1 year followed by use of a contraceptive method by the female may be desirable to encourage partnership in family planning. Although testosterone and other androgens suppress spermatogenesis in man, the feasibility of their use for contraception depends on the establishment of a dosage and mode of adminstration that provide antispermatogenic action without causing more general metabolic alterations. Inhibition of spermatogenesis by selective interference with the action of FSH on the Sertoli cells by active or passive immunization or by selective suppression of synthesis and release of FSH by administration of "Inhibin" offers exciting possibilities in the control of fertility in the male. Studies on the physiology of the rete testis highlight its importance as a post-tubular site of action of antifertility agents in conveying (to the epididymis) compounds interfering with epididymal functions and/or viability of spermatozoa. A new approach to the induction of functional sterility in the male by selective alteration of epididymal function by a local androgen deprivation effect has been successfully tested in clinical trials. Small doses of cyproterone acetate, administered orally, result in maintenance of libido and accessory sex gland function accompanied by a decrease in the motility of ejaculated spermatozoa and incomplete inhibition of spermatogenesis...

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抑制男性生育能力的靶点。
综述了男性生育控制的研究现状和前景。在男性生殖过程中,有两个潜在的位点可以作为男性生育调节的靶点:(1)抑制精子发生,(2)干扰附睾中的精子成熟。在实验动物身上测试的各种化合物的抗生精作用,由于许多不良的副作用,在控制人类男性的生育能力方面没有前途(cf. Prasad, 1973)。孕激素化合物通过影响下丘脑-垂体系统抑制精子发生,导致性欲受损。需要研究调节诱导抑制精子发生和血浆睾酮降低到与维持正常性欲和效力相容的水平所需的孕激素化合物的最小剂量的可能性。一种新的男性避孕方法是结合使用孕激素化合物来抑制精子发生,同时使用睾酮(通过硅胶胶囊植入或肌肉注射)来维持性欲和副性腺功能。许多这样的组合已经在临床试验中取得了一些成功。然而,副作用的局限性,如体重增加、男性乳房发育症和心理并发症,使其无法长期用于男性避孕。为了鼓励计划生育中的伙伴关系,男性短期使用这些联合方案1年,然后女性使用一种避孕方法可能是可取的。尽管睾酮和其他雄激素抑制男性的精子生成,但它们用于避孕的可行性取决于确定的剂量和给药方式,既能提供抗精子生成的作用,又不会引起更普遍的代谢改变。通过主动或被动免疫选择性地干扰卵泡刺激素对支持细胞的作用,或通过给予抑制素选择性地抑制卵泡刺激素的合成和释放,从而抑制精子发生,这为控制男性的生育能力提供了令人兴奋的可能性。对睾丸网生理学的研究强调了它作为抗生育药物在输送(到附睾)干扰附睾功能和/或精子活力的化合物时的管后作用部位的重要性。一种通过局部雄激素剥夺效应选择性改变附睾功能来诱导男性功能性不育的新方法已经成功地在临床试验中得到验证。口服小剂量醋酸环丙孕酮,可维持性欲和辅助性腺功能,同时降低射精精子的运动能力和不完全抑制精子发生。
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