Richardson B A, Vaughan M K, Petterborg L J, Johnson L Y, King T S, Smith I, Reiter R J
J Neural Transm. 1983;56(2-3):187-97. doi: 10.1007/BF01243277.
The potential antigonadotrophic properties of a number of synthetic and natural melatonin analogues were examined. Adult male hamsters received daily subcutaneous injections (25 micrograms/animal/day) each afternoon for 7 or 10 weeks. The only analogue to possess antigonadotrophic activity similar to melatonin wa 6-chloromelatonin; melatonin and 6-chloromelatonin produced a significant reduction in both testicular and accessory sex organ weights, plasma LH and pituitary prolactin. These results suggest that, in the Syrian hamster, 6-chloromelatonin acts as a melatonin agonist and may be of use to elucidate further the physiological role of melatonin.
研究了多种合成和天然褪黑素类似物的潜在抗促性腺激素特性。成年雄性仓鼠每天下午接受皮下注射(25微克/动物/天),持续7或10周。唯一具有与褪黑素类似的抗促性腺激素活性的类似物是6-氯褪黑素;褪黑素和6-氯褪黑素均使睾丸和附属生殖器官重量、血浆促黄体生成素(LH)和垂体催乳素显著降低。这些结果表明,在叙利亚仓鼠中,6-氯褪黑素作为褪黑素激动剂,可能有助于进一步阐明褪黑素的生理作用。