Gearhart J P, Linhard H R, Berkovitz G D, Jeffs R D, Brown T R
James Buchanan Brady Urological Institute, Johns Hopkins Hospital, Baltimore, Maryland.
J Urol. 1988 Nov;140(5 Pt 2):1243-6. doi: 10.1016/s0022-5347(17)42014-3.
The cause of hypospadias in the majority of patients is unknown. We examined the hypothesis that hypospadias might be explained by androgen receptor abnormalities in the atretic spongiosal tissue commonly known as chordee. We studied 10 patients with relatively severe hypospadias but with a predominantly male phenotype and no readily ascertained explanation for the defect, including no evidence of an abnormality in testosterone biosynthesis. Eight subjects had midshaft hypospadias and 2 had a penoscrotal meatus. All 10 patients had severe chordee. Serum concentrations of testosterone, and luteinizing and follicle-stimulating hormones were measured before human chorionic gonadotropin stimulation and a serum testosterone level was determined 24 hours after the last dose of a 5-day human chorionic gonadotropin stimulation (3,000 units per M.2 per day). Androgen receptor content and binding affinity were assayed in fibroblasts cultured from preputial skin and chordee tissue of patients and foreskin from normal male neonates. With the endogenous ligand dihydrotestosterone the mean number (maximum binding capacity) of androgen receptors was 1,013 fmol. per mg. deoxyribonucleic acid in preputial skin and 833 fmol. per mg. deoxyribonucleic acid in chordee tissue of patients, and 627 fmol. per mg. deoxyribonucleic acid in the foreskin of controls. With the nonmetabolizable, synthetic androgen methyltrienolone (R1881) the mean maximum binding capacity was 1,004, 722 and 758 fmol. per mg. deoxyribonucleic acid, respectively. Dihydrotestosterone receptor affinity (dissociation constant) was similar in preputial skin (0.20 nM.) and chordee tissue (0.21 nM.) from patients, and foreskin (0.29 nM.) from controls. Androgen receptor binding affinity of R1881 also was similar (0.30, 0.24 and 0.21 nM., respectively). Furthermore, the 5 alpha-reductase activity of preputial skin and chordee tissue of patients with hypospadias was similar to that of foreskin from normal neonates. In conclusion, isolated hypospadias in these subjects was not associated with androgen insensitivity of the spongiosal tissues on the basis of either decreased androgen receptor binding affinity, receptor number or conversion of testosterone to dihydrotestosterone.
大多数患者尿道下裂的病因尚不清楚。我们检验了一种假说,即尿道下裂可能是由通常称为阴茎硬结的闭锁海绵体组织中的雄激素受体异常所导致。我们研究了10例患有相对严重尿道下裂但主要表现为男性表型且无法轻易确定缺陷原因的患者,包括没有睾酮生物合成异常的证据。8名受试者患有阴茎中段尿道下裂,2名受试者有阴茎阴囊型尿道口。所有10例患者均有严重的阴茎硬结。在人绒毛膜促性腺激素刺激前测定睾酮、黄体生成素和促卵泡激素的血清浓度,并在5天的人绒毛膜促性腺激素刺激(每天每平方米体表面积3000单位)的最后一剂后24小时测定血清睾酮水平。对患者的包皮皮肤和阴茎硬结组织以及正常男性新生儿的包皮培养的成纤维细胞进行雄激素受体含量和结合亲和力测定。对于内源性配体双氢睾酮,患者包皮皮肤中雄激素受体的平均数量(最大结合容量)为每毫克脱氧核糖核酸1013飞摩尔,患者阴茎硬结组织中为每毫克脱氧核糖核酸833飞摩尔,对照组包皮中为每毫克脱氧核糖核酸627飞摩尔。对于不可代谢的合成雄激素甲基三烯醇酮(R1881),平均最大结合容量分别为每毫克脱氧核糖核酸1004、722和758飞摩尔。患者包皮皮肤(0.20纳摩尔)和阴茎硬结组织(0.21纳摩尔)以及对照组包皮(0.29纳摩尔)中的双氢睾酮受体亲和力(解离常数)相似。R1881的雄激素受体结合亲和力也相似(分别为0.30、0.24和0.21纳摩尔)。此外,尿道下裂患者的包皮皮肤和阴茎硬结组织的5α-还原酶活性与正常新生儿的包皮相似。总之,基于雄激素受体结合亲和力降低、受体数量减少或睾酮向双氢睾酮的转化,这些受试者的孤立性尿道下裂与海绵体组织的雄激素不敏感无关。