Nuclear Morphometric Analysis of Leydig Cells of Male Pubertal Rats Exposed In Utero to Di(n-butyl) Phthalate

We recently reported that prenatal rat exposure to di(n-butyl) phthalate (DBP) induced Leydig cell (LC) hyperplasia after nine weeks (wks) of age, yet the number of LCs was similar to that of the vehicle group until seven weeks. Nuclear pleomorphism of hyperplastic LCs is common and is considered to...

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Bibliographic Details
Published in:Journal of Toxicologic Pathology Vol. 26; no. 4; pp. 439 - 446
Main Authors: Wakui, Shin, Motohashi, Masaya, Satoh, Takemi, Shirai, Masaru, Mutou, Tomoko, Takahashi, Hiroyuki, Wempe, Michael F., Endou, Hitoshi, Inomata, Tomoo, Asari, Masao
Format: Journal Article
Language:English
Published: Japan JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY 2013
Japan Science and Technology Agency
Japanese Society of Toxicologic Pathology
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Summary:We recently reported that prenatal rat exposure to di(n-butyl) phthalate (DBP) induced Leydig cell (LC) hyperplasia after nine weeks (wks) of age, yet the number of LCs was similar to that of the vehicle group until seven weeks. Nuclear pleomorphism of hyperplastic LCs is common and is considered to be continuous progressive degeneration. Thus, computer-assisted image cell nuclear analysis of LCs was performed on 5- and 7-wk-old Sprague-Dawley (SD) rats whose dams had been administered DBP (i.g.) at 100 mg/kg/day or vehicle (corn oil) on gestation day 12 to 21. The results of the 5-wk-old DBP group were similar to those of the vehicle group; LC nuclei of the 7-wk-old DBP group showed normal ploidy and similar amounts of DNA. However, the size, elongation and peripheral chromatin aggregation parameters were significantly higher, and the reticular chromatin distribution and isolated chromatin aggregation parameters were significantly lower compared with the vehicle group. The present study quantitatively demonstrated nuclear morphological alterations in rat LCs at 7 wks old (puberty) due to the prenatal DBP administration before apparent LC hyperplasia developed.
ISSN:0914-9198
1881-915X
1347-7404
DOI:10.1293/tox.2013-0031