Cataldo N A, Cooper D S, Chin W W, Maloof F, Ridgway E C
Metabolism. 1982 Jun;31(6):589-94. doi: 10.1016/0026-0495(82)90097-x.
The effect of thyroid hormones and thyrotropin releasing hormone (TRH) on prolactin (PRL) secretion has been studied using a primary calf anterior pituitary cell culture system. After mechanical and enzymatic dispersion, cultured pituitary cells were preincubated with T3 or T4 for 48 hr prior to a 24 hr experimental incubation. T3 stimulated the release of PRL into the medium in a dose-related fashion, with an ED50 of 3 nM; at 10 nM T3, a maximal 52 +/- 5% stimulation (p less than 0.001) was observed. T4 at 100 nM stimulated medium PRL 27 +/- 10% (p less than 0.05); the ED50 for T4 was 20 nM. Neither T3 nor T4 affected intracellular PRL content. The stimulation of medium PRL by T3 was observed in medium containing 10% euthyroid as well as 10% charcoal-stripped hypothyroid calf serum. The relative stimulation by TRH of PRL release into the medium was significantly diminished by 10 nM T3 in euthyroid and stripped hypothyroid serum medium, but only as a consequence of the stimulation of basal medium PRL by T3; there was no change in maximal TRH-stimulated PRL release. In medium supplemented with unstripped hypothyroid serum, however, T3 did decrease absolute TRH-stimulated PRL release.
利用原代小牛垂体前叶细胞培养系统,研究了甲状腺激素和促甲状腺激素释放激素(TRH)对催乳素(PRL)分泌的影响。经机械和酶分散处理后,培养的垂体细胞在进行24小时实验性孵育前,先用T3或T4预孵育48小时。T3以剂量相关方式刺激PRL释放到培养基中,半数有效剂量(ED50)为3 nM;在10 nM T3时,观察到最大刺激为52±5%(p<0.001)。100 nM的T4刺激培养基中的PRL增加27±10%(p<0.05);T4的ED50为20 nM。T3和T4均不影响细胞内PRL含量。在含有10%正常甲状腺以及10%经活性炭处理的甲状腺功能减退小牛血清的培养基中,均观察到T3对培养基中PRL的刺激作用。在正常甲状腺和经处理的甲状腺功能减退血清培养基中,10 nM T3可使TRH刺激PRL释放到培养基中的相对刺激作用显著降低,但这只是T3刺激基础培养基中PRL的结果;TRH刺激的PRL最大释放量没有变化。然而,在补充未处理的甲状腺功能减退血清的培养基中,T3确实降低了TRH刺激的PRL绝对释放量。