Epididymal Epithelial Cell Involution Following a Single Intraperitoneal Administration of Ethane Dimethanesulfonate in the Goat (Capra hircus)

• Published in: Toxicology and applied pharmacology Vol. 175; no. 1; pp. 19 - 27
• Main Authors: Onyango, D.W., Wango, E.O., Werner, G.
• Format: Journal Article
• Language: English
• Published: San Diego, CA Elsevier Inc 15.08.2001; Elsevier
• Subjects: Animals; Biological and medical sciences; Capra hircus; Carcinogenesis, carcinogens and anticarcinogens; Chemical agents; degeneration; EDS; epididymis; Epididymis - cytology; Epididymis - drug effects; epithelium; Epithelium - drug effects; Epithelium - physiology; ethane dimethanesulfonate; Goats; Infusions, Parenteral; Male; Medical sciences; Mesylates - pharmacology; Tumors; epithelium; epididymis; EDS; degeneration; Intraperitoneal administration; Toxicity; Single dose; Leydig cell; Vertebrata; Epididymis; Mammalia; Histopathology; Ultrastructure; Animal; Epithelial cell; Goat; Artiodactyla; Male genital diseases; Ungulata
• DOI: 10.1006/taap.2001.9225
• ISSN: 0041-008X

Ethane dimethanesulfonate (EDS) selectively destroys Leydig cells in rats and a few other smaller animal species but not in mice and quail. In the teleost fish, it stimulates testicular activity instead. It also causes formation of sperm granulomas, reduction of sperm fertilizing ability, and destruction of clear cells in the epididymis. Investigations involving larger animal species are scanty. We have previously reported that EDS has no effect on goat Leydig cells but appears to have a direct cytotoxic effect on the seminiferous epithelium. This study was therefore designed to investigate the effects of EDS on goat epididymal cytoarchitecture. EDS was administered intraperitoneally at two dose levels, 75 and 25 mg/kg body wt. The former dose was rather toxic, killing three of five goats in this group within 24 h whereas the latter dose was well tolerated. Six days after treatment, the goats were hemicastrated and the epididymis was isolated and processed for light and electron microscopy. Involution associated with EDS was observed in epithelial cells of all regions of the epididymis, each having its own specific and peculiar changes. In the caput, there was increased cytoplasmic density accompanied by enlarged vacuoles and paucity of secretory vesicles in the apical cytoplasm. The Golgi cisternae were dilated and disorganized and, in the basal aspect, large dense staining bodies or inclusions, degenerative mitochondria, and lamellated bodies were observed. In the corpus, large vacuoles containing flocculent materials occurred in the entire cell cytoplasm but were particularly numerous and large in the midcytoplasm, completely obliterating the Golgi area. There was a dramatic reduction in epithelial height in the cauda epididymis accompanied by sparse distribution of markedly shortened microvilli. The epithelial cells had extensively lobulated nuclei and disorganized cytoplasm with dilated Golgi apparatus and large conglomerations of tubular structures. These structural changes suggest that EDS causes degeneration of goat epididymal epithelial cells. These effects are likely to result from the direct action of the compound on the epithelium.