Arslan M, Weinbauer G F, Schlatt S, Shahab M, Nieschlag E
Department of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
J Endocrinol. 1993 Feb;136(2):235-43. doi: 10.1677/joe.0.1360235.
The present study was designed to investigate the relative contributions of FSH and testosterone in the initiation of testicular growth and function in primates. Four groups (n = 4/group) of juvenile rhesus monkeys (Macaca mulatta), 12-18 months old, were treated with vehicle, a highly purified human FSH preparation (hFSH; Fertinorm, 3 IU/kg per day), testosterone (testosterone enanthate, 125 mg/week) or FSH plus testosterone, for a period of 12 weeks. Compared with vehicle treatment, the administration of hormones significantly (P < 0.05) increased testicular weight and volume, and the diameter of seminiferous tubules. The number of Sertoli cells per tubule cross-section also increased significantly (P < 0.05). Numbers of Ad (dark) spermatogonia (reserve stem cells) were not significantly influenced by any treatment. In contrast, the numbers of Ap (pale) spermatogonia (renewing stem cells) were significantly (P < 0.05) stimulated with hFSH and testosterone alone. Following the combined treatment, numbers of Ap spermatogonia were also higher compared with control but this effect did not attain statistical significance. In half of the animals in both testosterone-treated groups, a few prophase I spermatocytes were present. Inhibin concentrations reached adult levels in hFSH-treated groups but remained unaffected by testosterone. Conversely, testosterone failed to influence inhibin levels and, unlike hFSH, increased testicular androgen concentration and epididymal weights. Our observations suggest that hFSH and testosterone alone are capable of initiating testicular growth and gametogenesis in an immature primate. Both hormones probably act via activation of the proliferation of Ap spermatogonia, which are considered to be renewing stem cells within the testis.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究旨在调查促卵泡激素(FSH)和睾酮在灵长类动物睾丸生长启动及功能发挥过程中的相对作用。将四组(每组n = 4)12 - 18月龄的幼年恒河猴(猕猴)分别用赋形剂、高纯度人促卵泡激素制剂(hFSH;Fertinorm,每天3 IU/kg)、睾酮(庚酸睾酮,每周125 mg)或FSH加睾酮进行处理,为期12周。与赋形剂处理组相比,激素给药显著(P < 0.05)增加了睾丸重量和体积以及生精小管直径。每个小管横截面上支持细胞的数量也显著增加(P < 0.05)。任何处理对Ad(暗)精原细胞(储备干细胞)的数量均无显著影响。相反,单独使用hFSH和睾酮时,Ap(淡)精原细胞(更新干细胞)的数量受到显著(P < 0.05)刺激。联合处理后,Ap精原细胞数量与对照组相比也更高,但该效应未达到统计学显著性。在两个睾酮处理组的半数动物中,出现了一些减数分裂前期I的精母细胞。抑制素浓度在hFSH处理组达到成年水平,但不受睾酮影响。相反,睾酮未能影响抑制素水平,且与hFSH不同,它增加了睾丸雄激素浓度和附睾重量。我们的观察结果表明,单独使用hFSH和睾酮能够在未成熟灵长类动物中启动睾丸生长和配子发生。这两种激素可能都通过激活Ap精原细胞的增殖发挥作用,Ap精原细胞被认为是睾丸内的更新干细胞。(摘要截断于250字)