Davis J R, Vidal M E, Wilson E M, Sheppard M C
Department of Medicine, Queen Elizabeth Hospital, Edgbaston, Birmingham, England.
Acta Endocrinol (Copenh). 1989 May;120(5):672-6. doi: 10.1530/acta.0.1200672.
Two novel dopamine agonist drugs, CV 205-502 and CQP 201-403, have been investigated to compare their effects on prolactin secretion and prolactin mRNA accumulation in cultured rat pituitary cells. Both drugs gave dose-dependent suppression of prolactin release over a 24 h incubation period: when each drug was used at 100 nmol/l CV 205-502 and CQP 201-403 induced suppression to 8.9 +/- 1.7 and 10.2 +/- 1.8% of control release, respectively, compared to 26.7 +/- 4.8% of control with 100 nmol/l bromocriptine. There was no consistent effect on growth hormone release. Cytoplasmic accumulation of prolactin mRNA was also inhibited by both drugs at this concentration, to 50.2 +/- 5.5% of control values by CV 205-502 and to 67.4 +/- 8% of control by CQP 201-403, and to a similar extent by 100 nmol/l bromocriptine (50.6 +/- 9.1% of control). None of the drugs had any significant effect on GH mRNA levels. These data suggest that the agents exert their effect at a pretranslational stage of prolactin synthesis, as well as at the level of hormone release.
研究了两种新型多巴胺激动剂药物CV 205-502和CQP 201-403,比较它们对培养的大鼠垂体细胞中催乳素分泌和催乳素mRNA积累的影响。在24小时的孵育期内,两种药物均对催乳素释放产生剂量依赖性抑制:当每种药物以100 nmol/l使用时,CV 205-502和CQP 201-403分别将抑制作用诱导至对照释放的8.9±1.7%和10.2±1.8%,而100 nmol/l溴隐亭的对照释放为26.7±4.8%。对生长激素释放没有一致的影响。在该浓度下,两种药物也均抑制催乳素mRNA的细胞质积累,CV 205-502使其降至对照值的50.2±5.5%,CQP 201-403使其降至对照值的67.4±8%,100 nmol/l溴隐亭也有类似程度的抑制作用(对照值的50.6±9.1%)。这些药物对GH mRNA水平均无显著影响。这些数据表明,这些药物在催乳素合成的翻译前阶段以及激素释放水平发挥作用。