| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Endocrinology, Vol 127, 1215-1223, Copyright © 1990 by Endocrine Society
ARTICLES |
YT Sun, NG Wreford, DM Robertson and DM de Kretser
Department of Anatomy, Monash University, Clayton, Victoria, Australia.
A stereological study of the numbers of germ cells in various stages of spermatogenesis was undertaken in testosterone-treated intact and hypophysectomized (HPX) rats. Adult Sprague-Dawley rats were given testosterone by Silastic implants, which either inhibited (3-cm length) or partially maintained (10 cm) spermatogenesis over a 13-week period. The numbers of nuclei of the various germ cell categories (spermatogonia, spermatocytes, and round spermatids) in the testes were estimated by profile counting and measurement of nuclear diameter. The numbers of elongated spermatids were determined separately in testicular homogenates. Testis weight, seminiferous tubule volume, and tubule diameter were significantly decreased in intact rats with 3- and 10-cm testosterone implants and in HPX rats, although they were partially maintained in groups with 10-cm implants compared to those in groups with 3-cm implants (P less than 0.05). The effect of 3-cm testosterone implants in the intact group was to suppress the number of spermatogonia to 57%, reduce the conversion of spermatogonia to spermatocytes to 85%, and reduce the conversion of round to elongated spermatids to 19% of the control value. This latter effect was largely overcome with 10-cm testosterone implants. In HPX rats, only 10-cm implants were effective in maintaining the conversion of round spermatids to elongated spermatids. However, testosterone alone was less effective in maintaining the conversion of spermatocytes to round spermatids, suggesting that a pituitary factor, probably FSH, was involved. It is concluded that testosterone has a major effect on the conversion of round to elongated spermatids. The conversion of spermatogonia to spermatocytes and the conversion of spermatocytes to round spermatids depend on the synergistic action of both FSH and testosterone. However, the effect of FSH is greatest on the conversion of spermatocytes to spermatids, i.e. meiosis.
This article has been cited by other articles:
![]() |
S. J. Meachem, P. G. Stanton, and S. Schlatt Follicle-Stimulating Hormone Regulates Both Sertoli Cell and Spermatogonial Populations in the Adult Photoinhibited Djungarian Hamster Testis Biol Reprod, May 1, 2005; 72(5): 1187 - 1193. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Kanatsu-Shinohara, T. Morimoto, S. Toyokuni, and T. Shinohara Regulation of Mouse Spermatogonial Stem Cell Self-Renewing Divisionby the Pituitary Gland Biol Reprod, June 1, 2004; 70(6): 1731 - 1737. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. M. Allan, A. Garcia, J. Spaliviero, F.-P. Zhang, M. Jimenez, I. Huhtaniemi, and D. J. Handelsman Complete Sertoli Cell Proliferation Induced by Follicle-Stimulating Hormone (FSH) Independently of Luteinizing Hormone Activity: Evidence from Genetic Models of Isolated FSH Action Endocrinology, April 1, 2004; 145(4): 1587 - 1593. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Spaliviero, M. Jimenez, C. M. Allan, and D. J. Handelsman Luteinizing Hormone Receptor-Mediated Effects on Initiation of Spermatogenesis in Gonadotropin-Deficient (hpg) Mice Are Replicated by Testosterone Biol Reprod, January 1, 2004; 70(1): 32 - 38. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Haywood, J. Spaliviero, M. Jimemez, N. J. C. King, D. J. Handelsman, and C. M. Allan Sertoli and Germ Cell Development in Hypogonadal (hpg) Mice Expressing Transgenic Follicle-Stimulating Hormone Alone or in Combination with Testosterone Endocrinology, February 1, 2003; 144(2): 509 - 517. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. E. Keene, M. O. Suescun, M. G. Bostwick, V. Chandrashekar, A. Bartke, and J. J. Kopchick Puberty Is Delayed in Male Growth Hormone Receptor Gene--Disrupted Mice J Androl, September 1, 2002; 23(5): 661 - 668. [Abstract] [Full Text] [PDF] |
||||
![]() |
D.A. Jeyaraj, G. Grossman, C. Weaver, and P. Petrusz Dynamics of Testicular Germ Cell Proliferation in Normal Mice and Transgenic Mice Overexpressing Rat Androgen-Binding Protein: A Flow Cytometric Evaluation Biol Reprod, April 1, 2002; 66(4): 877 - 885. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. L. Smith, D. G. DeVera, D. J. Lamb, Z. Nawaz, Y.-H. Jiang, A. L. Beaudet, and B. W. O'Malley Genetic Ablation of the Steroid Receptor Coactivator-Ubiquitin Ligase, E6-AP, Results in Tissue-Selective Steroid Hormone Resistance and Defects in Reproduction Mol. Cell. Biol., January 15, 2002; 22(2): 525 - 535. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Yazawa, T. Yamamoto, Y. Jin, and S.-i. Abe Follicle-Stimulating Hormone Is Indispensable for the Last Spermatogonial Mitosis Preceding Meiosis Initiation in Newts (Cynops pyrrhogaster) Biol Reprod, January 1, 2002; 66(1): 14 - 20. [Abstract] [Full Text] |
||||
![]() |
N. G. Wreford, T. Rajendra Kumar, M. M. Matzuk, and D. M. de Kretser Analysis of the Testicular Phenotype of the Follicle-Stimulating Hormone {beta}-Subunit Knockout and the Activin Type II Receptor Knockout Mice by Stereological Analysis Endocrinology, July 1, 2001; 142(7): 2916 - 2920. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. K. O'Bryan, S. Schlatt, O. Gerdprasert, D. J. Phillips, D. M. de Kretser, and M. P. Hedger Inducible Nitric Oxide Synthase in the Rat Testis: Evidence for Potential Roles in Both Normal Function and Inflammation-Mediated Infertility Biol Reprod, November 1, 2000; 63(5): 1285 - 1293. [Abstract] [Full Text] |
||||
![]() |
Y. Lue, A. P. Sinha Hikim, C. Wang, M. Im, A. Leung, and R. S. Swerdloff Testicular Heat Exposure Enhances the Suppression of Spermatogenesis by Testosterone in Rats: The "Two-Hit" Approach to Male Contraceptive Development Endocrinology, April 1, 2000; 141(4): 1414 - 1424. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. K. O'Bryan, S. Schlatt, D. J. Phillips, D. M. de Kretser, and M. P. Hedger Bacterial Lipopolysaccharide-Induced Inflammation Compromises Testicular Function at Multiple Levels in Vivo Endocrinology, January 1, 2000; 141(1): 238 - 246. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. J. Handelsman, J. A. Spaliviero, J. M. Simpson, C. M. Allan, and J. Singh Spermatogenesis without Gonadotropins: Maintenance Has a Lower Testosterone Threshold than Initiation Endocrinology, September 1, 1999; 140(9): 3938 - 3946. [Abstract] [Full Text] |
||||
![]() |
Q. Wang, F. J. Ghadessy, A. Trounson, D. de Kretser, R. McLachlan, s. C. Ng, and E. L. Yong Azoospermia Associated with a Mutation in the Ligand-Binding Domain of an Androgen Receptor Displaying Normal Ligand Binding, but Defective Trans-Activation J. Clin. Endocrinol. Metab., December 1, 1998; 83(12): 4303 - 4309. [Abstract] [Full Text] |
||||
![]() |
J. Tesarik, M. Guido, C. Mendoza, and E. Greco Human Spermatogenesis in Vitro: Respective Effects of Follicle-Stimulating Hormone and Testosterone on Meiosis, Spermiogenesis, and Sertoli Cell Apoptosis J. Clin. Endocrinol. Metab., December 1, 1998; 83(12): 4467 - 4473. [Abstract] [Full Text] |
||||
![]() |
A. Meinhardt, M. Bacher, C. Metz, R. Bucala, N. Wreford, H. Lan, R. Atkins, and M. Hedger Local Regulation of Macrophage Subsets in the Adult Rat Testis: Examination of the Roles of the Seminiferous Tubules, Testosterone, and Macrophage-Migration Inhibitory Factor Biol Reprod, August 1, 1998; 59(2): 371 - 378. [Abstract] [Full Text] |
||||
![]() |
S. Maiti, J. Doskow, S. Li, R. P. Nhim, J. S. Lindsey, and M. F. Wilkinson The Pem Homeobox Gene. ANDROGEN-DEPENDENT AND -INDEPENDENT PROMOTERS AND TISSUE-SPECIFIC ALTERNATIVE RNA SPLICING J. Biol. Chem., July 19, 1996; 271(29): 17536 - 17546. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |