Seminiferous epithelium in adult rats was studied by light and electron microscopy after 5 weeks of chronic administration of GnRH antagonist (Ac-D2 Nal 1, D4ClPhe 2, DTrp 3, DArg 6, DAla 10; GnRH code-103-289-10, National Institutes of Health, USA). In these rats, the epithelium showed significant accumulation of vacuoles in more than 80% of the tubules, along with germ cell degeneration and nuclear pyknosis. Disruption in the process of spermatogenesis was also very much evident. In most of the tubules studied (greater than 90%), germ cell development was arrested beyond the pachytene spermatocyte stages. The vacuoles in the seminiferous epithelium were different sizes and when magnified were seen to consist of a thickened outer margin of solid nonfibrous coat within the Sertoli cell cytoplasm. Associated changes in the interstitium showed increased intertubular space but no inflammatory type of response. In actual cell counts, the decrease in the average number of macrophages was 32% and in Leydig cells 23%, while the total number of all types of cells in the interstitium was 30% less than that of the controls. Following the treatment, weights of testis, epididymis, seminal vesicle, and ventral prostate were drastically reduced. Rats treated with testosterone supplementation (60 micrograms/rat day) to GnRH antagonist recovered testicular and epididymal weights to approximately 57% and seminal vesicle and ventral prostate weights by 82.9 and 84%, respectively. Normalcy returned to the tubular epithelium and the interstitial cell counts were restored to original levels.
[1]
M. Misro,et al.
GnRH antagonist treatment affects nuclear size and membrane associated indentations in rat Leydig cells.
,
1991,
Archives of andrology.
[2]
R. Sharma,et al.
Effect of STS‐557 (17α‐cyanomethyl 17β‐hydroxy‐estra‐4, 9(10)‐dien‐3‐one) on blood hormone levels, the testis, accessory sex organs and fertility of rats
,
1990
.
[3]
R. Sharpe,et al.
Focal disruption of spermatogenesis in the testis of adult rats after a single administration of human chorionic gonadotrophin
,
1989,
Cell and Tissue Research.
[4]
R. Sharpe.
10 Paracrine control of the testis
,
1986
.
[5]
D. Kretser.
Sertoli cell — Leydig cell interaction in the regulation of testicular function
,
1982
.
[6]
O. Hovatta,et al.
Functional and Structural Aspects of the Rat Seminiferous Tubules after Treatment with Exogenous Cyproterone Acetate, Testosterone, Progesterone and Oestradiol
,
1978
.
[7]
G. Abraham.
Radioimmunoassay of steroids in biological materials.
,
1974
.
[8]
R. Sharpe,et al.
Effects and interactions of LH and LHRH agonist on testicular morphology and function in hypophysectomized rats.
,
1986,
Journal of reproduction and fertility.