Nappi C, Colace G, Di Renzo G F, Taglialatela M, Amoroso S, Annunziato L, Montemagno U
Eur J Clin Pharmacol. 1987;32(5):457-60. doi: 10.1007/BF00637669.
In the present study, 122 post puerperal women received at random bromoergocriptine, domperidone, bromoergocriptine plus domperidone or placebo treatment. Domperidone started 20-24 h after delivery and given for 10 or 15 days did not antagonize either the decrease in serum PRL induced by bromoergocriptine or the inhibition of lactation. It did suppress nausea and vomiting in the patients. The results are compatible with the idea that domperidone binds with a higher affinity than bromoergocriptine to DA (dopamine) receptors in the area postrema or the stomach. The converse phenomenon occurs at the level of the DA receptors on the PRL- secreting cells of the anterior pituitary gland.
在本研究中,122名产后妇女被随机给予溴隐亭、多潘立酮、溴隐亭加 多潘立酮或安慰剂治疗。多潘立酮在分娩后20 - 24小时开始给药,持续10或15天,既不拮抗溴隐亭引起的血清催乳素降低,也不抑制泌乳。它确实抑制了患者的恶心和呕吐。这些结果与以下观点相符,即多潘立酮比溴隐亭以更高的亲和力与最后区或胃中的多巴胺(DA)受体结合。相反的现象发生在垂体前叶催乳素分泌细胞的多巴胺受体水平。