Effects of Testosterone and Levonorgestrel Combined with a 5α-Reductase Inhibitor or Gonadotropin-Releasing Hormone Antagonist on Spermatogenesis and Intratesticular Steroid Levels in Normal Men

Context: Combination of a GnRH antagonist (acyline), types I and II, 5α-reductase inhibitor (dutasteride) or levonorgestrel (LNG) with testosterone (T) treatment may augment the suppression of spermatogenesis and intratesticular (iT) steroids. Objective: The objective of this study was to assess the...

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Published inThe journal of clinical endocrinology and metabolism Vol. 90; no. 10; pp. 5647 - 5655
Main Authors Matthiesson, Kati L., Stanton, Peter G., O’Donnell, Liza, Meachem, Sarah J., Amory, John K., Berger, Richard, Bremner, William J., McLachlan, Robert I.
Format Journal Article
LanguageEnglish
Published Bethesda, MD Oxford University Press 01.10.2005
Copyright by The Endocrine Society
Endocrine Society
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Online AccessGet full text
ISSN0021-972X
1945-7197
DOI10.1210/jc.2005-0639

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Abstract Context: Combination of a GnRH antagonist (acyline), types I and II, 5α-reductase inhibitor (dutasteride) or levonorgestrel (LNG) with testosterone (T) treatment may augment the suppression of spermatogenesis and intratesticular (iT) steroids. Objective: The objective of this study was to assess the effects of combined hormonal contraceptive regimens on germ cell populations and iT steroids. Design, Setting, and Participants: Twenty-nine normal health men enrolled in this prospective, randomized, 14-wk study at the University of Washington. Intervention(s): Twenty-two men (n = 5–6/group) received 8 wk of T enanthate (TE; 100 mg, im, weekly) combined with 1) 125 μg LNG daily, orally; 2) 125 μg LNG plus 0.5 mg dutasteride daily, orally; 3) 300 μg/kg acyline twice weekly, sc; or 4) 125 μg LNG daily, orally, plus 300 μg/kg acyline twice weekly, sc. Subjects then underwent a vasectomy and testicular biopsy. Control men (n = 7) proceeded directly to surgery. Main Outcome Measure(s): The main outcome measures were germ cells and iT steroids [T, dihydrotestosterone, 3α- and β-androstanediol (Adiol), and estradiol (E2)]. Results: High iT levels of all androgens (6- to 123-fold serum levels) and E2 (407-fold serum levels) were found in control men. iTT (1.9–2.6% control; P < 0.001) and iT3βAdiol (16–34% control; P < 0.05) levels decreased with all treatments. iT dihydrotestosterone (13–29% control; P < 0.05) and iT3αAdiol (44–47% control; P < 0.05) levels decreased with all but the TE plus LNG treatment. iTE2 levels decreased only in the TE plus acyline group (28% control; P = 0.01). Germ cells from type B spermatogonia onward were suppressed, with no differences between groups found. Variable sites of impairment of germ cell progression were evident between men (spermagonial maturation, meiosis 1 entry, and spermiation). Other than a negative correlation between iT3αAdiol and haploid germ cell number (P < 0.006), no correlations between germ cell number and gonadotropins, sperm concentration, or iT steroids were found. Conclusions: A similar high testicular:serum gradient exists for E2 and T in normal men, and 8 wk of gonadotropin suppression markedly reduces iTT, with 5α-reduced androgens and E2 levels decreasing to a much lesser degree. The heterogeneity of the germ cell response, regardless of treatment, gonadotropins or iT steroids, points to the individual sensitivity of sites in germ cell development, which is worthy of additional exploration.
AbstractList Context: Combination of a GnRH antagonist (acyline), types I and II, 5α-reductase inhibitor (dutasteride) or levonorgestrel (LNG) with testosterone (T) treatment may augment the suppression of spermatogenesis and intratesticular (iT) steroids. Objective: The objective of this study was to assess the effects of combined hormonal contraceptive regimens on germ cell populations and iT steroids. Design, Setting, and Participants: Twenty-nine normal health men enrolled in this prospective, randomized, 14-wk study at the University of Washington. Intervention(s): Twenty-two men (n = 5–6/group) received 8 wk of T enanthate (TE; 100 mg, im, weekly) combined with 1) 125 μg LNG daily, orally; 2) 125 μg LNG plus 0.5 mg dutasteride daily, orally; 3) 300 μg/kg acyline twice weekly, sc; or 4) 125 μg LNG daily, orally, plus 300 μg/kg acyline twice weekly, sc. Subjects then underwent a vasectomy and testicular biopsy. Control men (n = 7) proceeded directly to surgery. Main Outcome Measure(s): The main outcome measures were germ cells and iT steroids [T, dihydrotestosterone, 3α- and β-androstanediol (Adiol), and estradiol (E2)]. Results: High iT levels of all androgens (6- to 123-fold serum levels) and E2 (407-fold serum levels) were found in control men. iTT (1.9–2.6% control; P < 0.001) and iT3βAdiol (16–34% control; P < 0.05) levels decreased with all treatments. iT dihydrotestosterone (13–29% control; P < 0.05) and iT3αAdiol (44–47% control; P < 0.05) levels decreased with all but the TE plus LNG treatment. iTE2 levels decreased only in the TE plus acyline group (28% control; P = 0.01). Germ cells from type B spermatogonia onward were suppressed, with no differences between groups found. Variable sites of impairment of germ cell progression were evident between men (spermagonial maturation, meiosis 1 entry, and spermiation). Other than a negative correlation between iT3αAdiol and haploid germ cell number (P < 0.006), no correlations between germ cell number and gonadotropins, sperm concentration, or iT steroids were found. Conclusions: A similar high testicular:serum gradient exists for E2 and T in normal men, and 8 wk of gonadotropin suppression markedly reduces iTT, with 5α-reduced androgens and E2 levels decreasing to a much lesser degree. The heterogeneity of the germ cell response, regardless of treatment, gonadotropins or iT steroids, points to the individual sensitivity of sites in germ cell development, which is worthy of additional exploration.
Context: Combination of a GnRH antagonist (acyline), types I and II, 5α-reductase inhibitor (dutasteride) or levonorgestrel (LNG) with testosterone (T) treatment may augment the suppression of spermatogenesis and intratesticular (iT) steroids. Objective: The objective of this study was to assess the effects of combined hormonal contraceptive regimens on germ cell populations and iT steroids. Design, Setting, and Participants: Twenty-nine normal health men enrolled in this prospective, randomized, 14-wk study at the University of Washington. Intervention(s): Twenty-two men (n = 5–6/group) received 8 wk of T enanthate (TE; 100 mg, im, weekly) combined with 1) 125 μg LNG daily, orally; 2) 125 μg LNG plus 0.5 mg dutasteride daily, orally; 3) 300 μg/kg acyline twice weekly, sc; or 4) 125 μg LNG daily, orally, plus 300 μg/kg acyline twice weekly, sc. Subjects then underwent a vasectomy and testicular biopsy. Control men (n = 7) proceeded directly to surgery. Main Outcome Measure(s): The main outcome measures were germ cells and iT steroids [T, dihydrotestosterone, 3α- and β-androstanediol (Adiol), and estradiol (E2)]. Results: High iT levels of all androgens (6- to 123-fold serum levels) and E2 (407-fold serum levels) were found in control men. iTT (1.9–2.6% control; P < 0.001) and iT3βAdiol (16–34% control; P < 0.05) levels decreased with all treatments. iT dihydrotestosterone (13–29% control; P < 0.05) and iT3αAdiol (44–47% control; P < 0.05) levels decreased with all but the TE plus LNG treatment. iTE2 levels decreased only in the TE plus acyline group (28% control; P = 0.01). Germ cells from type B spermatogonia onward were suppressed, with no differences between groups found. Variable sites of impairment of germ cell progression were evident between men (spermagonial maturation, meiosis 1 entry, and spermiation). Other than a negative correlation between iT3αAdiol and haploid germ cell number (P < 0.006), no correlations between germ cell number and gonadotropins, sperm concentration, or iT steroids were found. Conclusions: A similar high testicular:serum gradient exists for E2 and T in normal men, and 8 wk of gonadotropin suppression markedly reduces iTT, with 5α-reduced androgens and E2 levels decreasing to a much lesser degree. The heterogeneity of the germ cell response, regardless of treatment, gonadotropins or iT steroids, points to the individual sensitivity of sites in germ cell development, which is worthy of additional exploration.
Author Amory, John K.
McLachlan, Robert I.
Matthiesson, Kati L.
Berger, Richard
Stanton, Peter G.
Bremner, William J.
Meachem, Sarah J.
O’Donnell, Liza
AuthorAffiliation Prince Henryʼs Institute of Medical Research and Department of Obstetrics and Gynecology, Monash University, Monash Medical Center (K.L.M., P.G.S., L.O., S.J.M., R.I.M.), Clayton, Victoria 3168, Australia; and Center for Research in Reproduction and Contraception, University of Washington (J.K.A., R.B., W.J.B.), Seattle, Washington 98195
AuthorAffiliation_xml – name: Prince Henryʼs Institute of Medical Research and Department of Obstetrics and Gynecology, Monash University, Monash Medical Center (K.L.M., P.G.S., L.O., S.J.M., R.I.M.), Clayton, Victoria 3168, Australia; and Center for Research in Reproduction and Contraception, University of Washington (J.K.A., R.B., W.J.B.), Seattle, Washington 98195
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  fullname: Meachem, Sarah J.
  organization: 1Prince Henry’s Institute of Medical Research and Department of Obstetrics and Gynecology, Monash University, Monash Medical Center (K.L.M., P.G.S., L.O., S.J.M., R.I.M.), Clayton, Victoria 3168, Australia
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  givenname: Richard
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  organization: 2Center for Research in Reproduction and Contraception, University of Washington (J.K.A., R.B., W.J.B.), Seattle, Washington 98195
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  givenname: William J.
  surname: Bremner
  fullname: Bremner, William J.
  organization: 2Center for Research in Reproduction and Contraception, University of Washington (J.K.A., R.B., W.J.B.), Seattle, Washington 98195
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  givenname: Robert I.
  surname: McLachlan
  fullname: McLachlan, Robert I.
  organization: 1Prince Henry’s Institute of Medical Research and Department of Obstetrics and Gynecology, Monash University, Monash Medical Center (K.L.M., P.G.S., L.O., S.J.M., R.I.M.), Clayton, Victoria 3168, Australia
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Issue 10
Keywords Human
Steroid
Androgen
Enzyme
Spermatogenesis
Levonorgestrel
Gonadotropin RH
Male
Progestagen
Hypothalamic hormone
Testosterone
Adult
Inhibitor
Testicular hormone
Oxidoreductases
Antagonist
Hormone releasing factor
Sex steroid hormone
Endocrinology
3-Oxo-5α-steroid 4-dehydrogenase
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Snippet Context: Combination of a GnRH antagonist (acyline), types I and II, 5α-reductase inhibitor (dutasteride) or levonorgestrel (LNG) with testosterone (T)...
CONTEXT:Combination of a GnRH antagonist (acyline), types I and II, 5α-reductase inhibitor (dutasteride) or levonorgestrel (LNG) with testosterone (T)...
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SubjectTerms 17β-Estradiol
Androgens
Biological and medical sciences
Biopsy
Cell number
Dihydrotestosterone
Endocrinopathies
Fundamental and applied biological sciences. Psychology
Germ cells
Gonadotropin-releasing hormone
Gonadotropins
Medical sciences
Meiosis
Pituitary (anterior)
Population studies
Serum levels
Sex hormones
Spermatogenesis
Spermatogonia
Steroid 5α-reductase
Steroids
Testes
Testosterone
Vertebrates: endocrinology
Title Effects of Testosterone and Levonorgestrel Combined with a 5α-Reductase Inhibitor or Gonadotropin-Releasing Hormone Antagonist on Spermatogenesis and Intratesticular Steroid Levels in Normal Men
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