Vanĕcek J
Institute of Physiology, Czechoslovak Academy of Sciences, Prague.
Neuroendocrinology. 1988 Aug;48(2):201-3. doi: 10.1159/000125008.
The development of melatonin receptors in the rat pituitary and median eminence was studied using [125I]melatonin as a ligand. The specific binding was detected in pituitaries of 20-day-old fetuses already. The affinity of the receptor to the ligand (Kd) was in the range 63-133 pM and it did not change significantly during development. The pituitary concentration of [125I]melatonin binding sites was highest in 20-day-old fetuses (Bmax = 31 fmol/mg protein) and then it gradually decreased in the course of postnatal development, until it reached 10% of that value in 29-day-old males. In contrast, the concentration of melatonin receptors in median eminence did not change markedly in the course of development and it was about 15 fmol/mg protein. The marked decrease in the number of the pituitary receptors may be the cause of the reported developmental loss of the melatonin inhibitory effect on LHRH-induced LH release from anterior pituitary.
使用[125I]褪黑素作为配体,研究了大鼠垂体和正中隆起中褪黑素受体的发育情况。在20日龄胎儿的垂体中已检测到特异性结合。受体对配体的亲和力(Kd)在63 - 133 pM范围内,在发育过程中无显著变化。[125I]褪黑素结合位点的垂体浓度在20日龄胎儿中最高(Bmax = 31 fmol/mg蛋白),然后在出生后发育过程中逐渐降低,直至在29日龄雄性大鼠中降至该值的10%。相反,正中隆起中褪黑素受体的浓度在发育过程中无明显变化,约为15 fmol/mg蛋白。垂体受体数量的显著减少可能是报道中褪黑素对促性腺激素释放激素诱导的垂体前叶促黄体生成素释放的抑制作用在发育过程中丧失的原因。