Hormonal regulation of spermatogenesis in the hypophysectomized rat: quantitation of germ-cell population and effect of elimination of residual testosterone after long-term hypophysectomy

• Published in: Journal of andrology Vol. 19; no. 3; pp. 335 - 340
• Main Authors: Franca, L. R, Parreira, G. G, Gates, R. J, Russell, L. D
• Format: Journal Article
• Language: English
• Published: Oxford, UK Am Soc Andrology 01-05-1998; Blackwell Publishing Ltd; American Society of Andrology
• Subjects: androgen; Androgen Antagonists - pharmacology; Animals; Biological and medical sciences; Body Weight; Flutamide - pharmacology; Fundamental and applied biological sciences. Psychology; germ cells; Hormone metabolism and regulation; Hypophysectomy; Male; Mammalian male genital system; morphometry; Organ Size; Rats; Rats, Sprague-Dawley; Seminiferous Tubules - anatomy & histology; Sperm Count; Spermatogenesis - physiology; Testis; Testis - cytology; Testosterone - antagonists & inhibitors; Testosterone - physiology; Vertebrates: reproduction; Androgen; Rat; Spermatogenesis; Rodentia; Male; Germinal cell; Long term; Testosterone; Vertebrata; Mammalia; Hypophysectomy; Testicular hormone; Sex steroid hormone; Morphometry; Viability
• ISSN: 0196-3635; 1939-4640
• DOI: 10.1002/j.1939-4640.1998.tb02012.x

Spermatogenesis continues after long‐term hypophysectomy (Hx), but massive cell degeneration prevents seminiferous tubules from attaining the full complement of cells. One objective of this study was to determine the vulnerable sites for completion of spermatogenesis in long‐term Hx rats. It is now known that Leydig cells continue to secrete small amounts of androgen after Hx. A second objective was to determine the cellular sites that are maintained by residual androgen secreted by Leydig cells post‐Hx. Two groups of adult animals were utilized. Both groups were Hx for 36 days, but one group of rats received the androgen antagonist flutamide during the 26th through the 36th day of Hx (10 days). Germ‐cell numbers were quantified using a method that allowed their expression as numbers of cells present per hour of development. In the long‐term Hx rat, the germ‐cell population increased to preleptotene, but the divisions that led to preleptotene were inefficient due to cell degeneration. Subsequent to preleptotene, there was a gradual loss in cells such that there were few germ cells remaining by steps 9–13. Flutamide given to Hx rats did not result in a significant difference in the numbers of intermediate and type B spermatogonia or significant differences in progenitor cells. A significant and major depression of cell numbers in Hx‐flutamide‐treated rats occurred in the cell division of type B spermatogonia to form preleptotene spermatocytes. There was a less dramatic, although significant, depression of cell numbers in Hx‐flutamide—treated animals that occurred from preleptotene until late pachytene as well as an increased loss of round spermatids at midcycle (step 5–6). These data demonstrate that cell loss after long‐term Hx occurs at numerous phases of spermatogenesis. The data also demonstrate that the presence of residual androgen action after long‐term Hx results in enhanced germ‐cell survival. Although the major blockage in cell viability occurs at midcycle steps in the long‐term Hx rat, there are several other hormone‐sensitive phases of spermatogenesis.