Sinha Y N, Salocks C B, VanderLaan W P
Horm Metab Res. 1976 Sep;8(5):332-6. doi: 10.1055/s-0028-1093627.
The influence of 2-bromo-alpha-ergocryptine (CB-154) and 2-chloro-6-methyl-ergoline-8beta-acetonitrile methanesulfonate (lergotrile mesylate) on prolactin (PRL) and growth hormone (GH) secretion in mice was investigated. Both drugs inhibited the nursing-induced rise in serum PRL in lactating mice, CB-154 being effective at a somewhat lower dosage than lergotrile mesylate. Both drugs reduced basal concentrations of serum PRL by more than 90% within an hr after administration, but the effect of CB-154 lasted for several hr longer than that of lergotrile mesylate. CB-154 did not change the resting concentrations of GH in mice, but it promoted the induction of GH release by nursing; injection of lergotrile mesylate, on the other hand, seemed to enhance the basal concentrations of GH in lactating mice that were separated from their young for 12 hr. The results show that both drugs can be used successfully for reducing PRL secretion in the mouse.
研究了2-溴-α-麦角隐亭(CB-154)和2-氯-6-甲基麦角灵-8β-乙腈甲磺酸盐(甲磺酸麦角腈)对小鼠催乳素(PRL)和生长激素(GH)分泌的影响。两种药物均抑制哺乳期小鼠因哺乳引起的血清PRL升高,CB-154在比甲磺酸麦角腈稍低的剂量下即有效。两种药物在给药后1小时内均使血清PRL基础浓度降低90%以上,但CB-154的作用持续时间比甲磺酸麦角腈长数小时。CB-154未改变小鼠GH的静息浓度,但促进了哺乳诱导的GH释放;另一方面,注射甲磺酸麦角腈似乎提高了与幼崽分离12小时的哺乳期小鼠的GH基础浓度。结果表明,两种药物均可成功用于降低小鼠的PRL分泌。