Turpen C, Knigge K M
Horm Res. 1979;11(3):128-41. doi: 10.1159/000179048.
An acute incubation procedure, using explanted normal rat hemipituitaries pretreated with fresh plasma obtained from pituitary donor animals, was employed to further investigate the in vitro stimulation of prolactin (PRL release by thyrotropin-releasing hormone (TRH). Pretreatment with dopamine (0.1 microgram/ml) caused a 30-50% decrease in the amount of PRL released into incubation media; the inhibitory effect of dopamine was not reversed by treatment with 0.5-6.0 ng. TRH, although these TRH concentrations consistently stimulated PRL release from pituitaries not exposed to dopamine. Treatment with thyroxine (10(-6) to 10(-5) M) showed a competitive inhibition of thyrotropin release by TRH (0.5 ng), but was without effect on TRH-stimulated PRL release. Cycloheximide (100 microgram/ml) blocked a net increase in PRL levels. TRH, nevertheless, significantly increased PRL release in the presence of cycloheximide. The results indicate that neither dopamine nor thyroxine compete with TRH in causing PRL release, and that the TRH stimulation of PRL release is unrelated to ongoing levels of hormone synthesis.
采用一种急性孵育程序,即使用取自垂体供体动物的新鲜血浆预处理的正常大鼠半垂体进行体外孵育,以进一步研究促甲状腺激素释放激素(TRH)对催乳素(PRL)释放的体外刺激作用。用多巴胺(0.1微克/毫升)预处理可使释放到孵育培养基中的PRL量减少30 - 50%;多巴胺的抑制作用不会因用0.5 - 6.0纳克TRH处理而逆转,尽管这些TRH浓度能持续刺激未接触多巴胺的垂体释放PRL。用甲状腺素(10⁻⁶至10⁻⁵摩尔/升)处理显示对TRH(0.5纳克)刺激的促甲状腺激素释放有竞争性抑制作用,但对TRH刺激的PRL释放无影响。放线菌酮(100微克/毫升)可阻止PRL水平的净增加。然而,在存在放线菌酮的情况下,TRH仍能显著增加PRL释放。结果表明,多巴胺和甲状腺素在引起PRL释放方面均不与TRH竞争,且TRH对PRL释放的刺激作用与激素合成的现有水平无关。