Oh Jin Kyu, Im Young Jae, Park Kwanjin, Paick Jae-Seung
Department of Urology, College of Medicine, Gachon University, Incheon, Republic of Korea.
Department of Urology, College of Medicine, Seoul National University, Seoul, Republic of Korea.
Endocr Connect. 2018 Nov;7(11):1150-1157. doi: 10.1530/EC-18-0200.
Although it is well known that penile growth is dependent on androgens, few clinical studies have reported successful treatment of micropenis with testosterone, likely due to concerns regarding the efficacy and safety of prolonged testosterone use. Thus, we assessed the synergenic effects of growth hormone (GH) treatments with and without testosterone on phallic growth in a rat model of micropenis. Fifty Sprague-Dawley rats were assigned to control (C), microphallus (MP), testosterone, GH (G) and GH plus testosterone (GT) treatment groups, and microphallus was induced by secondary hypogonadism. Pre-pubertal treatments with testosterone, GH or the combination were initiated from 7 days after birth and were maintained until 12 weeks of age. To assess the efficacy of treatments, phallic dimensions were determined and histological markers of cavernosal integrity were evaluated. Skeletal and gonadal safety profiles of the treatments were then assessed according to right tibial lengths and testicular weights, respectively. No monotreatments normalised penile dimensions, whereas combination treatments led to complete restoration. The combination treatment also prevented decreases in histological indicators of cavernosal integrity, including smooth muscle actin and collagen III expression levels and fat globule accumulation and sinusoidal density. These synergenic effects of GH treatments on penile growth may follow changes in androgen receptor expression levels and were accompanied by decreased testicular volume losses. Although the physiological conditions of phallic growth differ between humans and rats, this proof-of-concept study provides a strategy for circumventing the problems of testosterone monotherapy for human micropenis.
尽管众所周知阴茎生长依赖雄激素,但很少有临床研究报道使用睾酮成功治疗小阴茎,这可能是由于担心长期使用睾酮的疗效和安全性。因此,我们在小阴茎大鼠模型中评估了生长激素(GH)单独或联合睾酮治疗对阴茎生长的协同作用。将50只Sprague-Dawley大鼠分为对照组(C)、小阴茎组(MP)、睾酮组、生长激素组(G)和生长激素加睾酮组(GT),通过继发性性腺功能减退诱导小阴茎形成。从出生后7天开始对青春期前的大鼠进行睾酮、生长激素或联合治疗,并持续至12周龄。为评估治疗效果,测定阴茎尺寸并评估海绵体完整性的组织学标志物。然后分别根据右胫骨长度和睾丸重量评估治疗的骨骼和性腺安全性。单一治疗均未使阴茎尺寸恢复正常,而联合治疗导致阴茎尺寸完全恢复。联合治疗还防止了海绵体完整性组织学指标的下降,包括平滑肌肌动蛋白和胶原蛋白III表达水平、脂肪球积聚和血窦密度。生长激素治疗对阴茎生长的这些协同作用可能与雄激素受体表达水平的变化有关,并伴有睾丸体积减少的减轻。尽管人类和大鼠阴茎生长的生理条件不同,但这项概念验证研究为规避人类小阴茎睾酮单一疗法的问题提供了一种策略。