Publications of Faculty of Medicine:EFFECTS OF LONG-TERM ADMINISTRATION OF TESTOSTERONE ON THE STRUCTURE OF ADULT ALBINO RAT PROSTATE: Abstract

Title:
EFFECTS OF LONG-TERM ADMINISTRATION OF TESTOSTERONE ON THE STRUCTURE OF ADULT ALBINO RAT PROSTATE
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Abstract:

Abstract The increasing use of testosterone in male contraception has necessitated evaluation of the effects of testosterone on the structure of the prostate gland, which is androgen dependent. Twenty eight adult male albino rats were divided into two equal groups (control and treated groups). The control group (7) was srihrlinided into two equal subgroups. The subgroup Ia served as a basic control (no treatment). The subgroup lb was injected I.M. with 0.5 ml sesame oil once per week for three months. The treated group (II) was injected LM. with testosterone enanthate 10mg / kg body weight once per week for three months. The prostate glands were removed under ether anaesthesia and prepared for light and electron microscopic examination. The results of this study showed that the prostatic acirti of control rats were lined by simple columnar secretory cells with small basal cells in between- These cells were supported by a basement membrane and thrown into internal papillae. The acirti were separated from each other by a loose connective tissue. The columnar secretory cells could be divided into two types. Type I cells were characterized by a pale staining cytoplasm and a large vesicular nucleus with prominent nucleolus and a narrow peripheral rim of heterochromatitt. Type II cells had more abundant dark staining cytoplasm and dark nucleus with a wide band of peripheral heterochromatin. The columnar secretory cells were characterized by a well-developed rough endoplasmic reticulum, secretory granules and mien:milli on the lumenal surfaces In the treated group, the long-term administration of testosterone for three months induced changes in the structure and secretory activity of pros tatic acirti. These changes were: (1) Increasing of the heights ql secretory cells, (2) Increasing of the mitotic activities of these cells. (3) Loss of normal cellular ar-