Progesterone catabolizing enzyme, the enzyme 20α-hydroxysteroid deltydrgenase(20α-HSD) is pivotal in the regulation of ovarian function in rodents, which catabolizes progesterone into biologically inactive 20α hydroxypregn-4-en-3-one(20α-OHP). In this study was carried out the influence of 20α-HSD activity to ovarian function and regulation such as ovulation, formation of corpus luteum, maintenance of estrous cycles and pregnancy, we investigated changes in activities of the splenic macrophages and ovarian histological findings in rat.
During the estrous cycles, the ratious of phagocytotic macrophage in splenic adherent cells were highest of the proestrous, but they were lowest on metestrous. During the pregnancy, the ratious of phagocytotic macrophages in splenic adhrent cells were lowest by 1 day and then significantly increased toward the pregnancy, which were highest pregnancy on day 12. On histological findings in rat ovary, the mean number of growing, antral and mature follicles were 15.9(72.9%), 3.4(15.9%), and 2.4(11.2%), respectively. Growing follicles reached to lowest number at diestrus and mature follicle reached to lowest number at metestrus. The numbers of corpus luteums per tissue section of tlae ovary were 14.4 and the number of normal and atretic follicles were 11.0(76.4%) and 3.4(23.0%), respectively. The number of corpus luteum with vacolated cell were 1.7(11.8%).
In this study suggests splenic macrophages are as a source of the substance which maintainer progesterone secretion from luteal cells, and are recognized pass the vessels and reside in the fresh corpora lutea soon after ovulation via inflammatory reactions, and these macrophages are felt to have a stimulatory effect on the formation of croloora lutea. In view of the results include previous report^(14), ovarian 20α-hydroxysteroid dehydrogenase enzyme and splen ic macrophages consider play central role in the control and maintenance of estrous cycles and pregnancy, and also applicable to both clinical and research in a N2de variety such as control of reproductive system.
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