Literature DB >> 11459772

Testosterone and estrogen act via different pathways to inhibit puberty in the male Siberian hamster (Phodopus sungorus).

T R Pak1, G R Lynch, P S Tsai.   

Abstract

The peripubertal transition in male mammals is accompanied by a gradual decrease in sensitivity to the inhibitory effects exerted by gonadal hormones, such as T and E2. Here, we investigated the effects of chronic T and its metabolites, 5alpha-dihydrotestosterone and E2 on the hypothalamo-pituitary-gonadal axis at puberty. We also examined if T effects are distinct or mediated through its conversion to 5alpha-dihydrotestosterone or E2. Twenty-day-old male Siberian hamsters were sc implanted with a SILASTIC brand capsule containing varying doses of T, 5alpha-dihydrotestosterone, or E2. Several functional parameters of the hypothalamo-pituitary-gonadal axis were evaluated including hypothalamic GnRH concentration, pituitary and plasma FSH levels, pituitary FSH and LH mRNA, and testicular status. Our results showed that gonadal steroids inhibited puberty in a dose-dependent manner as evaluated by testes mass (undiluted steroid: T, 27 +/- 3 mg; 5alpha-dihydrotestosterone, 18 +/- 1 mg; and E2, 62 +/- 4 mg relative to cholesterol-implanted controls, 510 +/- 42 mg). Also, T decreased plasma FSH below detectable levels, but pituitary FSH concentration was unaffected (1.37 +/- 0.16 ng/microg protein) while E2-treated hamsters had normal plasma FSH levels (3.5 +/- 0.98 ng/ml) yet significantly lower pituitary FSH concentration (0.09 +/- 0.04 ng/microg protein). These results showed that the pathways of T and E2 action on the hypothalamo-pituitary-gonadal axis are distinct.

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Year:  2001        PMID: 11459772     DOI: 10.1210/endo.142.8.8321

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  6 in total

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Authors:  Yathindar S Rao; Natasha N Mott; Toni R Pak
Journal:  Endocrine       Date:  2011-03-09       Impact factor: 3.633

2.  Opposite-sex housing reactivates the declining GnRH system in aged transgenic male mice with FGF signaling deficiency.

Authors:  Johanna R Rochester; Wilson C J Chung; Tyrone B Hayes; Pei-San Tsai
Journal:  Am J Physiol Endocrinol Metab       Date:  2012-10-09       Impact factor: 4.310

3.  Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice.

Authors:  John Falardeau; Wilson C J Chung; Andrew Beenken; Taneli Raivio; Lacey Plummer; Yisrael Sidis; Elka E Jacobson-Dickman; Anna V Eliseenkova; Jinghong Ma; Andrew Dwyer; Richard Quinton; Sandra Na; Janet E Hall; Celine Huot; Natalie Alois; Simon H S Pearce; Lindsay W Cole; Virginia Hughes; Moosa Mohammadi; Pei Tsai; Nelly Pitteloud
Journal:  J Clin Invest       Date:  2008-08       Impact factor: 14.808

4.  The effect of testosterone, dihydrotestosterone and oestradiol on the re-initiation of spermatogenesis in the adult photoinhibited Djungarian hamster.

Authors:  Sarah J Meachem; Stefan Schlatt; Saleela M Ruwanpura; Peter G Stanton
Journal:  J Endocrinol       Date:  2007-03       Impact factor: 4.286

5.  Alteration of the hypothalamic-pituitary-gonadal axis in estrogen- and androgen-treated adult male leopard frog, Rana pipiens.

Authors:  Pei-San Tsai; Ann E Kessler; Jeremy T Jones; Kathleen B Wahr
Journal:  Reprod Biol Endocrinol       Date:  2005-01-10       Impact factor: 5.211

6.  Fgf8-Deficient Mice Compensate for Reduced GnRH Neuronal Population and Exhibit Normal Testicular Function.

Authors:  Wei Zhang; Joshua I Johnson; Pei-San Tsai
Journal:  Front Endocrinol (Lausanne)       Date:  2015-09-22       Impact factor: 5.555

  6 in total

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