van Bergeijk L, Gooren L J
Horm Metab Res. 1986 Apr;18(4):272-6. doi: 10.1055/s-2007-1012292.
This study was designed to investigate the role of endogenous oestrogens in the dopaminergic regulation of prolactin and TSH release in 16 normogonadotrophic oligozoospermic men. Three months' administration of the oestrogen-receptor antagonist tamoxifen (10 mg twice daily), blocking oestrogen-receptors both in the CNS and peripherally, did not affect basal prolactin and TSH levels. Neither was the prolactin or TSH response to stimulation with the anti-dopaminergic agents metoclopramide (10 mg i.v.) (acting both in the CNS and peripherally) and domperidone (10 mg i.v.) (acting peripherally) affected by tamoxifen administration. The response of prolactin and TSH to metoclopramide proved to be no greater than to domperidone. It is concluded that: Endogenous oestrogens, in as far as receptor-mediated, do not affect basal or anti-dopaminergic stimulated release of both prolactin and TSH in normogonadotrophic oligozoospermic men. The anti-dopaminergic activity of metoclopramide in the release of prolactin and TSH is likely for the greater part peripheral.
本研究旨在调查内源性雌激素在16名正常促性腺激素性少精子症男性催乳素和促甲状腺激素释放的多巴胺能调节中的作用。给予雌激素受体拮抗剂他莫昔芬(每日两次,每次10 mg)三个月,阻断中枢神经系统和外周的雌激素受体,并未影响基础催乳素和促甲状腺激素水平。他莫昔芬的给药也未影响催乳素或促甲状腺激素对抗多巴胺能药物甲氧氯普胺(静脉注射10 mg)(在中枢神经系统和外周均起作用)和多潘立酮(静脉注射10 mg)(在外周起作用)刺激的反应。事实证明,催乳素和促甲状腺激素对甲氧氯普胺的反应并不比对多潘立酮的反应更大。得出以下结论:就受体介导而言,内源性雌激素不影响正常促性腺激素性少精子症男性催乳素和促甲状腺激素的基础释放或抗多巴胺能刺激释放。甲氧氯普胺在催乳素和促甲状腺激素释放中的抗多巴胺能活性可能大部分在外周。