Corbin A, Beattie C W, Jones R, Bex F
Int J Gynaecol Obstet. 1979 Mar-Apr;16(5):359-72. doi: 10.1002/j.1879-3479.1979.tb00466.x.
A prototype LH-RH antagonist dampened the proestrous gonadotropin surge and blocked ovulation but had no effect on pregnant animals. In contrast, LH-RH and two highly potent LH-RH agonists terminated pregnancy when administrated prior to or following implantation. This contragestational effect, as well as other antireproductive properties of the agonists, coupled with the reversibility of their effects, strongly suggest that peptides may provide a new basis for contraception.
一种促黄体生成素释放激素(LH-RH)拮抗剂原型可抑制动情前期促性腺激素激增并阻止排卵,但对妊娠动物无效。相比之下,促黄体生成素释放激素(LH-RH)和两种高效的促黄体生成素释放激素激动剂在植入前或植入后给药时可终止妊娠。这种抗孕作用以及激动剂的其他抗生殖特性,再加上其作用的可逆性,有力地表明肽类可能为避孕提供新的基础。