Seppälä M, Unnérus H A, Hirvonen E, Ranta T
J Clin Endocrinol Metab. 1976 Aug;43(2):474-7. doi: 10.1210/jcem-43-2-474.
In a series of 23 patients bromocriptine increased the plasma estradiol-17 beta level from 44.0 +/- 9.5 (mean +/- SE) to 144.1 +/- 31.8 pg/ml after 3 - 5 weeks' treatment (p less than 0.01). In normoprolactinemic patients (N = 12) the level increased from 59.6 +/- 16.3 to 186.5 +/- 50.5 pg/ml (p less than 0.05), and in hyperprolactinemic patients (N = 11) the corresponding values were 27.0 +/- 6.2 and 97.8 +/- 34.6 pg/ml (p less than 0.05). Bromocriptine treatment did not significantly alter the FSH and LH levels. The results suggest that bromocriptine treatment induces endocrine recovery also in patients whose clinical findings give no indication of prolactin suppression.
在一组23例患者中,经3至5周的治疗后,溴隐亭使血浆雌二醇-17β水平从44.0±9.5(均值±标准误)升高至144.1±31.8 pg/ml(p<0.01)。在血催乳素正常的患者(n = 12)中,该水平从59.6±16.3升高至186.5±50.5 pg/ml(p<0.05),而在高催乳素血症患者(n = 11)中,相应数值分别为27.0±6.2和97.8±34.6 pg/ml(p<0.05)。溴隐亭治疗未显著改变促卵泡激素(FSH)和促黄体生成素(LH)水平。结果表明,对于临床检查未显示催乳素受抑制迹象的患者,溴隐亭治疗也能促使内分泌恢复。