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Journal of Endocrinology (2007) 193, 127-135       DOI: 10.1677/joe.1.06975
© 2007 Society for Endocrinology
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The role of glucocorticoid in the regulation of prostaglandin biosynthesis in non-pregnant bovine endometrium

Hwa-Yong Lee, Tomas J Acosta, Michiyo Tanikawa, Ryosuke Sakumoto1, Junichi Komiyama, Yukari Tasaki, Mariusz Piskula2, Dariusz J Skarzynski3, Masafumi Tetsuka4 and Kiyoshi Okuda

Laboratory of Reproductive Endocrinology, Graduate School of Natural Science and Technology, Okayama University, Okayama 700-8530, Japan
1 Department of Physiology and Genetic Regulation, National Institute of Agrobiological Sciences, Ibaraki 305-0901, Japan
2 Departments of Food Technology and
3 Reproductive Immunology, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn 10-747, Poland
4 Department of Agricultural and Life Science, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido 080-8555, Japan

(Requests for offprints should be addressed to K Okuda; Email: kokuda{at}cc.okayama-u.ac.jp)

To determine whether glucocorticoids (GCs) play a role in regulating uterine function in cow, the present study examined the expression of mRNA encoding GC receptor (GC-R) {alpha}, 11ß-hydroxysteroid dehydrogenase (11-HSD) type 1 and type 2, and the activity of 11-HSD1 in bovine endometrial tissue throughout the estrous cycle. We also studied the effects of cortisol on basal, oxytocin (OT)- and tumor necrosis factor-{alpha} (TNF{alpha})-stimulated prostaglandin (PG) production. A quantitative real-time PCR analysis revealed that GC-R{alpha} mRNA was expressed more strongly in the mid-luteal stage (days 8–12) than in the other stages. In contrast to GC-R{alpha} mRNA expression, 11-HSD1 mRNA expression was greater in the follicular stage than in the other stages, whereas 11-HSD2 mRNA expression was lowest in the follicular stage. The activity of 11-HSD1 was greater in the follicular stage and estrus than in the other stages and was lowest in the mid-luteal stage. Cortisone was dose-dependently converted to cortisol in the cultured endometrial tissue. Although cortisol did not affect either the basal or OT-stimulated production of PGs in the cultured epithelial cells, the production of PGs stimulated by TNF{alpha} in the stromal cells was suppressed by cortisol (P < 0.05). Cortisol suppressed basal prostaglandin (PG)F2{alpha} without affecting basal PGE2 production in the stromal cells. The overall results suggest that the level of cortisol is locally regulated in bovine endometrium throughout the estrous cycle by 11-HSD1, and that cortisol could act as a luteoprotective factor by selectively suppressing luteolytic PGF2{alpha} production in bovine endometrium.




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