Importance of inhibin B in the regulation of FSH secretion in the human male.

Détails

ID Serval
serval:BIB_A78BE3D4F9C5
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Importance of inhibin B in the regulation of FSH secretion in the human male.
Périodique
Journal of Clinical Endocrinology and Metabolism
Auteur⸱e⸱s
Hayes F.J., Pitteloud N., DeCruz S., Crowley W.F., Boepple P.A.
ISSN
0021-972X (Print)
ISSN-L
0021-972X
Statut éditorial
Publié
Date de publication
2001
Peer-reviewed
Oui
Volume
86
Numéro
11
Pages
5541-5546
Langue
anglais
Notes
Publication types: Clinical Trial ; Journal Article
Résumé
Regulation of FSH secretion in the male involves a complex balance between stimulation by GnRH from the hypothalamus, inhibitory feedback by sex steroids (T and E2) and inhibin B (Inh B) from the gonads, and autocrine/paracrine modulation by activin and follistatin within the pituitary. The aim of the present study was to delineate the feedback control of FSH in the human male with specific reference to the relative roles of sex steroids vs. Inh B. Two experimental human models were used: 1) normal (NL) men subjected to acute sex steroid withdrawal (-T, -E2, + Inh B), and 2) functional castrate males (-T, -E2, -Inh B). Nine NL men (age range, 25-45 yr) and three castrate males (age range, 23-47 yr) were studied. The NL men underwent acute sex steroid suppression using high dose ketoconazole (1-g loading dose, followed by 400 mg, orally, four times daily for 150 h). Gonadotropin secretion was characterized by frequent blood sampling every 10 min for 12 h at baseline and on d 3 and 6 of sex steroid ablation. In the three castrate subjects, blood sampling was performed every 5 min for 24 h 8 wk after discontinuing androgen replacement therapy. In the NL men, treatment with ketoconazole resulted in a decline to castrate levels in T (451 +/- 20 to 38 +/- 7 ng/dl; P < 0.0005) and E2 (39 +/- 4 to 15 +/- 2 pg/ml; P < 0.005) and a modest, but significant, decline in Inh B levels, which remained within the normal range (183 +/- 19 to 136 +/- 13 pg/ml; P < 0.005). This suppression of sex steroids was associated with a more marked increase in mean LH (9.5 +/- 0.9 to 24.9 +/- 2.0 IU/liter; P < 0.0001) than FSH levels (5.1 +/- 0.7 to 10.0 +/- 1.5 IU/liter; P < 0.005), with the latter not exceeding the normal adult male range. The castrate subjects had a mean T level of 66 +/- 8 ng/dl, an E2 level of 20 +/- 1 pg/ml, and undetectable Inh B levels. Despite a similar sex steroid milieu, the mean FSH levels observed in NL men after acute sex steroid ablation were approximately 6-fold lower than those seen in the castrate subjects (10.0 +/- 1.5 vs. 59.5 +/- 17.7 IU/liter; P < 0.0005). In contrast, mean LH levels in the NL men were less than 3-fold lower than those in castrate subjects (24.9 +/- 2.0 vs. 66.8 +/- 20.1 IU/liter; P < 0.005). From this human model of acute sex steroid withdrawal, we conclude that Inh B is likely to be the major feedback regulator of FSH secretion in the human male.
Mots-clé
Adult, Estradiol/blood, Feedback/physiology, Follicle Stimulating Hormone/blood, Follicle Stimulating Hormone/metabolism, Hormone Antagonists/pharmacology, Humans, Inhibins/blood, Inhibins/physiology, Ketoconazole/pharmacology, Luteinizing Hormone/blood, Male, Middle Aged, Neurosecretory Systems/physiology, Orchiectomy, Testosterone/blood
Pubmed
Open Access
Oui
Création de la notice
03/12/2014 16:43
Dernière modification de la notice
20/08/2019 16:12
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