McCartney Christopher R, Bellows Amy B, Gingrich Melissa B, Hu Yun, Evans William S, Marshall John C, Veldhuis Johannes D
Center for Research in Reproduction, Division of Endocrinology, Department of Internal Medicine, University of Virginia Health System, Charlottesville, VA 22908, USA.
Am J Physiol Endocrinol Metab. 2004 Jun;286(6):E902-8. doi: 10.1152/ajpendo.00415.2003. Epub 2004 Jan 21.
Studies using pharmacological gonadotropin stimulation suggest that ovarian steroidogenesis is abnormal in the polycystic ovary syndrome (PCOS). We assessed ovarian steroid secretion in response to near-physiological gonadotropin stimuli in 12 ovulatory controls and 7 women with PCOS. A gonadotropin-releasing hormone-receptor antagonist (ganirelix, 2 mg sc) was given to block endogenous LH secretion, followed by dexamethasone (0.75 mg orally) to suppress adrenal androgen secretion. After ganirelix injection (12 h), intravenous infusions of recombinant human LH (0, 10, 30, 100, and 300 IU; each over 8 min) were administered at 4-h intervals in a pseudorandomized (highest dose last) manner. Plasma LH, 17-hydroxyprogesterone (17-OHP), androstenedione, and testosterone were measured concurrently. LH dose-steroid response relationships (mean sex-steroid concentration vs. mean LH concentration over 4 h postinfusion) were examined for each subject. Linear regression of 17-OHP on LH yielded a higher (mean +/- SE) slope in PCOS (0.028 +/- 0.010 vs. 0.005 +/- 0.005, P < 0.05), whereas extrapolated 17-OHP at zero LH was similar. The slopes of other regressions did not differ from zero in either PCOS or controls. We conclude that near-physiological LH stimulation drives heightened 17-OHP secretion in patients with PCOS, suggesting abnormalities of early steps of ovarian steroidogenesis. With the exception of 17-OHP response in PCOS, no acute LH dose-ovarian steroid responses were observed in controls or PCOS. Defining the precise mechanistic basis of heightened precursor responsiveness to LH in PCOS will require further clinical investigation.
使用药物性促性腺激素刺激的研究表明,多囊卵巢综合征(PCOS)患者的卵巢类固醇生成异常。我们评估了12名排卵正常的对照者和7名PCOS女性在接近生理水平的促性腺激素刺激下的卵巢类固醇分泌情况。给予促性腺激素释放激素受体拮抗剂(醋酸加尼瑞克,2mg皮下注射)以阻断内源性LH分泌,随后给予地塞米松(0.75mg口服)以抑制肾上腺雄激素分泌。在注射醋酸加尼瑞克(12小时)后,以伪随机方式(最高剂量最后给予)每隔4小时静脉输注重组人LH(0、10、30、100和300IU;每次持续8分钟)。同时测定血浆LH、17-羟孕酮(17-OHP)、雄烯二酮和睾酮。检查了每个受试者的LH剂量-类固醇反应关系(输注后4小时内平均性类固醇浓度与平均LH浓度)。17-OHP对LH的线性回归在PCOS患者中产生了更高的(平均值±标准误)斜率(0.028±0.010对0.005±0.005,P<0.05),而LH为零时的外推17-OHP相似。在PCOS患者或对照者中,其他回归的斜率均无统计学差异。我们得出结论,接近生理水平的LH刺激会导致PCOS患者17-OHP分泌增加,提示卵巢类固醇生成早期步骤存在异常。除了PCOS患者中17-OHP的反应外,在对照者或PCOS患者中均未观察到急性LH剂量-卵巢类固醇反应。明确PCOS患者中前体对LH反应性增强的确切机制基础需要进一步的临床研究。