Gold M S, Donabedian R K, Redmond D E
Endocrinology. 1978 Apr;102(4):1183-9. doi: 10.1210/endo-102-4-1183.
Intravenous administration of 2,5 mg/kg piperoxane produced a rapid and significant increase in serum PRL concentrations in four non-human primates. This PRL increase was maximal 15 min after piperoxane infusion and significant, when compared with baseline levels, in the +15, +30, +45, +60, and +90-min samples. The iv administration of 5 mg/kg piperoxane also produced a rapid and significant increase, whereas saline 0.5 mg/kg or 1.0 mg/kg, did not change serum PRL levels. The iv administration of 10 microgram/kg clonidine, but not saline, produced a rapid and significant reduction in serum PRL levels. PRL levels were significantly reduced +15, +30, and +60 min after the clonidine infusion. Pretreatment with a bolus of 10 microgram/kg clonidine at -15 min caused a significant attenuation of the piperoxane-induced elevation in serum PRL in two monkeys. These data support the hypothesis that alpha-adrenergic receptors are involved in the inhibition of PRL secretion. These data are compatible with noradrenergic or adrenergic mechanisms which remain to be defined.
对四只非人灵长类动物静脉注射2.5毫克/千克的哌罗克生后,血清催乳素(PRL)浓度迅速显著升高。这种PRL升高在输注哌罗克生后15分钟达到最大值,与基线水平相比,在输注后15、30、45、60和90分钟时的样本中差异显著。静脉注射5毫克/千克的哌罗克生也能迅速显著升高PRL,而0.5毫克/千克或1.0毫克/千克的生理盐水则不会改变血清PRL水平。静脉注射10微克/千克的可乐定(而非生理盐水)能迅速显著降低血清PRL水平。在输注可乐定后15、30和60分钟时,PRL水平显著降低。在输注前15分钟静脉注射一剂10微克/千克的可乐定,可使两只猴子中哌罗克生诱导的血清PRL升高显著减弱。这些数据支持α-肾上腺素能受体参与抑制PRL分泌这一假说。这些数据与有待确定的去甲肾上腺素能或肾上腺素能机制相符。