Literature DB >> 19265279

Collaborative work on evaluation of ovarian toxicity. 12) Effects of 2- or 4-week repeated dose studies and fertility study of indomethacin in female rats.

Kenjiro Tsubota1, Kiyoshi Kushima, Kenji Yamauchi, Seiki Matsuo, Tadashi Saegusa, Shin Ito, Michio Fujiwara, Masahiro Matsumoto, Shunji Nakatsuji, Jiro Seki, Yuji Oishi.   

Abstract

2-week and 4-week general toxicity studies of indomethacin, a nonselective inhibitor of cyclooxygenase 1 and 2, were performed using rats. A female fertility study was also conducted to compare the results to those of ovarian histopathological findings. The main purposes of the present studies are to assess whether a precise histopathological examination, taking the morphological changes the female reproductive organs undergo during each estrus phases into account, can evaluate toxicity to the ovaries, and to determine the optimal administration period for detecting ovarian toxicity. Indomethacin was administered on a daily basis to female Sprague-Dawley rats at doses of 0, 0.4, 1.3, or 4 mg/kg in the both the general toxicity studies and the female fertility study. In the general toxicity studies, unruptured follicles or luteinized cysts were observed histopathologically in the 4 mg/kg group in both the 2-week and 4-week studies. In addition, follicular cysts were found in the 4 mg/kg group in the 4-week study. Estrous cyclicity was not disturbed in both studies. There were no histopathological changes in the ovaries of the 1.3 mg/kg group in general toxicity studies. In the female fertility study, no toxic effects on female fertility parameters were detected in the 0.4 and 1.3 mg/kg group treated with indomethacin, but 8 of 10 rats in the 4 mg/kg group died or were sacrificed before completion of the dosing period. These results demonstrated that 2 weeks of indomethacin treatment is sufficient to detect unruptured follicles or luteinized cyst in the ovary. In addition, 4 weeks of dosing maybe required for induction of follicular cysts, although we could not clearly show that these histopathological changes would affect female fertility functions. These present studies suggest that a precise histopathological examination may be able to predict the effect of test articles on female reproductive functions.

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Year:  2009        PMID: 19265279     DOI: 10.2131/jts.34.s129

Source DB:  PubMed          Journal:  J Toxicol Sci        ISSN: 0388-1350            Impact factor:   2.196


  3 in total

1.  Impact of luteinized unruptured follicles on endometrial receptivity.

Authors:  Wangming Xu; Jing Yang; Lei Jiang; Jing Hu
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2011-04-20

Review 2.  Nonproliferative and proliferative lesions of the rat and mouse female reproductive system.

Authors:  Darlene Dixon; Roger Alison; Ute Bach; Karyn Colman; George L Foley; Johannes H Harleman; Richard Haworth; Ronald Herbert; Anke Heuser; Gerald Long; Michael Mirsky; Karen Regan; Eric Van Esch; F Russell Westwood; Justin Vidal; Midori Yoshida
Journal:  J Toxicol Pathol       Date:  2014       Impact factor: 1.628

Review 3.  Luteal toxicity evaluation in rats.

Authors:  Yoshikazu Taketa
Journal:  J Toxicol Pathol       Date:  2021-11-18       Impact factor: 1.628

  3 in total

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