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      Testosterone and Dihydrotestosterone, but Not Estradiol, Selectively Maintain Pituitary and Serum Follicle-Stimulating Hormone in Gonadotropin-Releasing Hormone Antagonist Treated Male Rats

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          Abstract

          Recently it has been found that testosterone can maintain and restimulate serum and pituitary follicle-stimulating hormone (FSH) in the gonadotropin-releasing hormone (GnRH) antagonist treated adult male rat. The present investigation was undertaken to determine (1) which metabolite of testosterone, dihydrotestosterone (DHT), or estradiol accounts for the effects of testosterone in GnRH antagonist suppressed rats and (2) whether these effects of testosterone are influenced by other testicular factors. Eight groups of 6–8 adult male Sprague-Dawley rats were subjected to the following treatments: vehicle, GnRH antagonist (75 µg/day s.c), testosterone-filled Silastic implants (3 × 5 cm, s.c), DHT-filled Silastic implants (3 × 5 cm, s.c), estradiol ben-zoate (15 µg/day s.c), and combined administration of GnRH antagonist with either steroid. In addition, the GnRH antagonist/ testosterone treatment regimen was applied to rats orchidectomized 72 h prior to initiation of treatments. After 3 weeks of treatment, serum was analyzed for concentrations of luteinizing-hormone (LH), FSH, testosterone, DHT, and estradiol. Pituitary extracts were analyzed for LH and FSH content. Except for the vehicle-treated groups, serum and pituitary LH concentrations were markedly suppressed by all treatments. In intact rats treated with GnRH antagonist alone and/or estradiol, the pituitary FSH level was reduced by more than 70% relative to controls, while both testosterone and DHT maintained pituitary FSH. Similarly, testosterone and DHT, but not estradiol, delayed the decline of serum FSH induced with GnRH antagonist alone. In orchidectomized animals, testosterone was also capable of preventing a reduction of pituitary FSH despite concomitant GnRH antagonist administration. It is concluded that testosterone and DHT selectively maintain FSH in the GnRH antagonist treated male rat. This paradoxical stimulation of FSH occurs in the absence of other testicular factors.

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          Author and article information

          Journal
          NEN
          Neuroendocrinology
          10.1159/issn.0028-3835
          Neuroendocrinology
          S. Karger AG
          0028-3835
          1423-0194
          1989
          1989
          02 April 2008
          : 49
          : 4
          : 395-401
          Affiliations
          Max Planck Clinical Research Unit for Reproductive Medicine and Department of Reproductive Medicine, University of Münster, FRG
          Article
          125144 Neuroendocrinology 1989;49:395–401
          10.1159/000125144
          2497399
          © 1989 S. Karger AG, Basel

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          Page count
          Pages: 7
          Categories
          Original Paper

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