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少精子症男性的雄激素不敏感:重新评估

Androgen insensitivity in oligospermic men: a reappraisal.

作者信息

Bouchard P, Wright F, Portois M C, Couzinet B, Schaison G, Mowszowicz I

出版信息

J Clin Endocrinol Metab. 1986 Nov;63(5):1242-6. doi: 10.1210/jcem-63-5-1242.

Abstract

Androgen insensitivity has been reported to be present in as many as 40% of patients with severe oligospermia. In order to evaluate further the role of androgen resistance in male infertility we studied 24 men with severe oligospermia. Plasma T and LH were measured by RIA and the T X LH product was calculated. Fibroblasts were grown from genital skin obtained during testicular biopsies and androgen receptor maximal binding capacity (BMAX) and affinity (KD) were measured in fibroblast monolayers. Pubic skin 5 alpha-reductase activity, an androgen-dependent enzyme, was measured in skin homogenates. Plasma T values were in the upper normal range [7.0 +/- 1.7 (SEM) ng ml-1] whereas the T X LH product was high (greater than 50) in only six patients. Mean BMAX and KD values for the androgen receptor were normal [BMAX: 788 +/- 259 fmol mg DNA-1 (patients, n = 20), 726 +/- 227 (normal men, n = 20), and KD: 0.27 +/- 0.24 (patients, n = 20), 0.18 +/- 0.09 (normal men, n = 15), respectively]. However, four men had supranormal KD values. The mean BMAX was also normal when the group of men with sperm densities below 10(6) per ejaculate was considered separately. Public skin 5 alpha-reductase activity was normal in all but four patients (patients: 177.1 +/- 91 fmol/mg skin/h, n = 30, normal men: 210 +/- 45, n = 20 patients). In conclusion, androgen receptor BMAX levels were normal in all patients studied, regardless of the sperm density and the T X LH product. Pubic skin 5 alpha-reductase activity was also normal in all but four patients. In these four patients, a qualitative defect of the androgen receptor cannot be excluded. In this group of patients with severe oligospermia, infertility did not seem to be related to quantitative abnormality of the androgen receptor as was previously reported.

摘要

据报道,高达40%的严重少精子症患者存在雄激素不敏感。为了进一步评估雄激素抵抗在男性不育中的作用,我们研究了24名严重少精子症男性。采用放射免疫分析法测定血浆睾酮(T)和促黄体生成素(LH),并计算T×LH乘积。从睾丸活检时获取的生殖器皮肤培养成纤维细胞,并在成纤维细胞单层中测定雄激素受体的最大结合容量(BMAX)和亲和力(KD)。在皮肤匀浆中测定雄激素依赖性酶——耻骨皮肤5α-还原酶活性。血浆T值处于正常上限[7.0±1.7(标准误)ng/ml-1],而仅6例患者的T×LH乘积较高(大于50)。雄激素受体的平均BMAX和KD值正常[BMAX:788±259 fmol/mg DNA-1(患者,n = 20),726±227(正常男性,n = 20);KD:0.27±0.24(患者,n = 20),0.18±0.09(正常男性,n = 15)]。然而,4名男性的KD值超常。当单独考虑精子密度低于每射精10⁶个的男性组时,平均BMAX也正常。除4例患者外,所有患者的耻骨皮肤5α-还原酶活性均正常(患者:177.1±91 fmol/mg皮肤/h,n = 30;正常男性:210±45,n = 20例患者)。总之,在所研究的所有患者中,无论精子密度和T×LH乘积如何,雄激素受体BMAX水平均正常。除4例患者外,所有患者的耻骨皮肤5α-还原酶活性也正常。在这4例患者中,不能排除雄激素受体存在定性缺陷。在这组严重少精子症患者中,不育似乎与先前报道的雄激素受体定量异常无关。

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