Melis G B, Gambacciani M, Paoletti A M, Mais V, Cagnacci A, Petacchi F D, Fioretti P
Neuroendocrinology. 1985 Aug;41(2):138-41. doi: 10.1159/000124167.
To evaluate whether ovarian steroids modify the prolactin (PRL) response to opioid receptor blockade, the effects of naloxone infusion (1.6 mg/h for 4 h) on PRL secretion were studied in 5 postmenopausal women. Naloxone infusion was performed in basal conditions and after chronic oral treatment with conjugated estrogens (CE) (1.25 mg/day, for 20 days) or CE plus medroxyprogesterone acetate (MPA) (10 mg/day, for 20 days). Under basal conditions, 17 beta-estradiol, estrone, gonadotropin, and PRL plasma levels were in the normal range for postmenopausal women, and naloxone failed to affect PRL secretion. Naloxone induced a significant PRL increase after CE treatment alone (p less than 0.001) or in combination with MPA (p less than 0.001). The increase was significantly higher (p less than 0.05) after CE + MPA treatment than after CE treatment alone. These data suggest that steroids modulate the stimulatory effect of naloxone on PRL secretion in postmenopausal women.
为评估卵巢类固醇是否改变催乳素(PRL)对阿片受体阻断的反应,我们对5名绝经后女性研究了纳洛酮输注(1.6毫克/小时,共4小时)对PRL分泌的影响。纳洛酮输注在基础状态下进行,以及在接受共轭雌激素(CE)(1.25毫克/天,共20天)或CE加醋酸甲羟孕酮(MPA)(10毫克/天,共20天)的慢性口服治疗后进行。在基础状态下,17β-雌二醇、雌酮、促性腺激素和PRL血浆水平处于绝经后女性的正常范围内,纳洛酮未能影响PRL分泌。单独使用CE治疗(p<0.001)或与MPA联合使用(p<0.001)后,纳洛酮可引起PRL显著升高。CE + MPA治疗后的升高显著高于单独使用CE治疗(p<0.05)。这些数据表明,类固醇可调节纳洛酮对绝经后女性PRL分泌的刺激作用。