Author:
GAREM YEHIA F. EL,ARINI ALI F. EL,BEHEIRY ADEL H. EL,ZEID SAMI A. ABOU,COMHAIRE FRANK H.
Abstract
ABSTRACT: Inhibin B is bidirectionally secreted by Sertoli cells, basal secretion into the circulation exerts negative feedback on follicle‐stimulating hormone secretion, and serum inhibin B is considered a marker of spermatogenesis. The precise role of apical secretion is unknown. The objective of our work was to study the relationship between seminal inhibin B and spermatogenesis. Dimeric inhibin B was measured by immunoassay in seminal plasma of volunteers with normozoospermia (n = 10, group 1), in men after vasectomy (n = 10, group 2), and in men with azoospermia (n = 50, group 3). Testicular biopsy and testicular sperm extraction were performed in men with azoospermia. Seminal inhibin B levels were higher in men in group 1 than in men in groups 2 and 3 (P < .0001). In seminal plasma, inhibin B presents a positive correlation with alpha glucosidase activity (r = .37, P = .002). Seminal inhibin B is inversely related with serum FSH (r = ‐.58, P < .001), and presents a weak positive correlation with serum testosterone concentration (r = .29, P = .03). No difference was found between inhibin B levels in seminal plasma of patients with nonobstructive or obstructive azoospermia, and between positive or negative outcome of TESE. We conclude that inhibin B secretion by Sertoli cells is differentially regulated. The contribution of accessory sex glands limits the use of seminal plasma inhibin B as a marker of spermatogenesis.
Subject
Urology,Endocrinology,Reproductive Medicine,Endocrinology, Diabetes and Metabolism
Cited by
2 articles.
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