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[双氢麦角汀的降血催乳素活性]

[Blood prolactin-lowering activity of dihydroergocristine].

作者信息

Cocchi D, Müller E E, Boselli P, Faini D

出版信息

Farmaco Sci. 1985 Jul;40(7):534-40.

PMID:3930286
Abstract

The prolactin lowering activity of dihydroergocristine, a dihydrogenated ergopeptine derivative, was evaluated in male rats. The drug caused a significant decrease of prolactin levels both in the normoprolactinemic animals and in reserpine-induced hyperprolactinaemia at 5 mg/kg p.o. while 0.2 and 1 mg/kg p.o. were ineffective. In a second experiment the prolactin lowering activity of dihydroergocristine (0.2; 1.5 mg/kg), in reserpine-induced hyperprolactinaemia was compared with bromocryptine (0.1; 0.5; 2.5 mg/kg) administered intraperitoneally. Both dihydroergocristine and bromocryptine caused a significant decrease of prolactin plasma concentrations at all dose levels. Moreover the prolactin lowering effect was independent of the dose administered. Our data suggest prolactin lowering activity of oral or i.p. dihydroergocristine both on normal plasma concentrations and on the experimentally-induced hypersecretion of the hormone.

摘要

在雄性大鼠中评估了二氢麦角隐亭(一种双氢麦角肽衍生物)降低催乳素的活性。该药物在口服剂量为5mg/kg时,对正常催乳素水平的动物和利血平诱导的高催乳素血症动物均能显著降低催乳素水平,而口服剂量为0.2mg/kg和1mg/kg时则无效。在第二个实验中,将二氢麦角隐亭(0.2mg/kg;1.5mg/kg)在利血平诱导的高催乳素血症中的降低催乳素活性与腹腔注射的溴隐亭(0.1mg/kg;0.5mg/kg;2.5mg/kg)进行了比较。二氢麦角隐亭和溴隐亭在所有剂量水平下均能显著降低催乳素血浆浓度。此外,降低催乳素的作用与给药剂量无关。我们的数据表明,口服或腹腔注射二氢麦角隐亭对正常血浆浓度以及实验诱导的激素分泌过多均有降低催乳素的活性。

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