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[溴隐亭对多囊卵巢综合征内分泌环境的影响]

[Effects of bromocriptine on endocrine environment in the polycystic ovary syndrome].

作者信息

Huang H J, Ishimaru T, Yamabe T

机构信息

Department of Obstetric and Gynecology, School of Medicine, Nagasaki University, Japan.

出版信息

Nihon Naibunpi Gakkai Zasshi. 1988 Apr 20;64(4):265-78. doi: 10.1507/endocrine1927.64.4_265.

Abstract

In order to investigate the hormone feature and the effect of bromocriptine on endocrine profile in patients with polycystic ovary syndrome (PCO), twenty-four-hour secretion pattern of LH, FSH, PRL and testosterone were assessed in 8 PCO patients and 4 normal women as controls by obtaining serial blood samples, taken through a forearm cannula, at 30 minute intervals for 24 hours. Bromocriptine, 5 mg/day was given and 3 patients were reassessed in the follicular phase of the menstrual cycle after ovulatory periods were established during bromocriptine therapy. There was significant difference in pulse amplitude, but not in pulse frequency of LH and testosterone between PCO and normal women (23.1 +/- 9.49 vs 5.75 +/- 1.28 mIU/ml, p less than 0.01; 27.8 +/- 10.1 vs 10.2 +/- 2.63 ng/dl, p less than 0.01), and the 24 hour mean LH and testosterone levels were higher (p less than 0.01) in PCO (52.3 +/- 20.1 mIU/ml, 105.1 +/- 15.9 ng/dl) than in normal women (13.4 +/- 4.31 mIU/ml, 54.3 +/- 13.3 ng/dl). Though a pulsatility in FSH secretion was identified, no difference between normal women and PCO was observed. Mean PRL level was within the normal range in PCO but with a higher pulse frequency (p less than 0.01) and lower pulse amplitude (p less than 0.01) than those of the normal women. Furthermore, LH and testosterone secretions maintained the circadian changes in PCO patients against the normal women. During bromocriptine therapy, mean level and pulse amplitude of LH and testosterone were significantly suppressed, without changing in pulse frequency, whilst PRL secretory patterns were not reestablished. In conclusion we have found that PCO is associated with high level and pulse amplitude of LH and testosterone, with high frequency and low amplitude of PRL, and bromocriptine administration can blunt LH, PRL and testosterone secretion, suggesting a hypothalamic intervention in gonadotropic regulation in patient with PCO. In addition, the degree of bromocriptine to inhibit LH secretion might be related to the dose or duration of its administration, or to the sensitivity of the patients. The mechanism of bromocriptine for marked LH suppression in PCO patients remains to be elucidated.

摘要

为了研究多囊卵巢综合征(PCO)患者的激素特征以及溴隐亭对其内分泌状况的影响,通过在前臂留置套管,以30分钟的间隔连续采集血样24小时,评估了8例PCO患者和4例正常女性作为对照的LH、FSH、PRL和睾酮的24小时分泌模式。给予溴隐亭5mg/天,并在溴隐亭治疗期间建立排卵周期后的月经周期卵泡期对3例患者进行重新评估。PCO患者与正常女性之间LH和睾酮的脉冲幅度存在显著差异,但脉冲频率无差异(23.1±9.49对5.75±1.28mIU/ml,p<0.01;27.8±10.1对10.2±2.63ng/dl,p<0.01),PCO患者的24小时平均LH和睾酮水平高于正常女性(p<0.01)(52.3±20.1mIU/ml,105.1±15.9ng/dl),而正常女性为(13.4±4.31mIU/ml,54.3±13.3ng/dl)。虽然发现FSH分泌存在脉冲性,但未观察到正常女性与PCO患者之间存在差异。PCO患者的平均PRL水平在正常范围内,但与正常女性相比,脉冲频率较高(p<0.01),脉冲幅度较低(p<0.01)。此外,与正常女性相比,PCO患者的LH和睾酮分泌保持昼夜变化。在溴隐亭治疗期间,LH和睾酮的平均水平及脉冲幅度被显著抑制,脉冲频率未改变,而PRL分泌模式未恢复。总之,我们发现PCO与LH和睾酮的高水平及脉冲幅度、PRL的高频率和低幅度相关,给予溴隐亭可抑制LH、PRL和睾酮分泌,提示对PCO患者的促性腺激素调节存在下丘脑干预。此外,溴隐亭抑制LH分泌的程度可能与其给药剂量或持续时间有关,或与患者的敏感性有关。溴隐亭显著抑制PCO患者LH分泌的机制仍有待阐明。

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