Saddick Salina Y
Biological Studies Dept., Faculty of Science, King Abdulaziz University, PO Box 42671, Jeddah 21551, Saudi Arabia.
Saudi J Biol Sci. 2014 Jul;21(3):232-7. doi: 10.1016/j.sjbs.2014.02.004. Epub 2014 Mar 13.
The present study is designed to demonstrate the ovarian surface epithelial cells' (OSE) estrogen receptor α (ERα) and progesterone receptor (PR) during pregnancy and estrous cycle in rat. Moreover, determination of the levels of plasma progesterone, estradiol, FSH and LH was also made. The levels of plasma progesterone, estradiol, FSH and LH concentrations were determined on days 7 (n = 5), 14 (n = 5), and 21 (n = 5) of pregnancy in three groups of rats and during the estrous cycle (n = 5) using an ELISA kit. Immunohistochemical method for PR and ERα expressions was also made on the ovary. During pregnancy, FSH and LH remained low except at term when LH levels began to increase from 16 ng/ml to 47 ng/ml. Progesterone levels significantly exceeded estradiol values in all pregnant rats with a peak value of 202 ng/ml on day 14. Elevated progesterone levels were associated negatively with LH and estradiol levels during pregnancy. The levels of estradiol surged significantly on day 21. Immunohistochemistry of the ovary showed low levels of OSE cells staining positive for ERα expression. ERα positive cells were absent on day 7 and 14 of pregnancy, only day 21 recorded a very low percentage of immunostaining (0.5%) within the nuclei of OSE cells. On the contrary, immunostaining of PR was not observed within the nuclei of OSE cells in all groups of study. In conclusion, these results may suggest that the progesterone effect during pregnancy seems to be overriding the positive effect of estrogens on OSE cells. High progesterone levels may have a direct negative effect on gonadotropin production and thereby it might inhibit events leading to both follicular development and OSE proliferation. Understanding the factors affecting OSE proliferation may help elucidating the mechanism(s) of assisted diseases such as ovarian cancer.
本研究旨在证明大鼠妊娠和发情周期期间卵巢表面上皮细胞(OSE)的雌激素受体α(ERα)和孕激素受体(PR)。此外,还测定了血浆孕酮、雌二醇、促卵泡激素(FSH)和促黄体生成素(LH)的水平。使用酶联免疫吸附测定(ELISA)试剂盒,在三组大鼠的妊娠第7天(n = 5)、第14天(n = 5)和第21天(n = 5)以及发情周期(n = 5)期间,测定血浆孕酮、雌二醇、FSH和LH的浓度。还采用免疫组织化学方法检测卵巢中PR和ERα的表达。在妊娠期间,FSH和LH一直保持在低水平,直到足月时LH水平才开始从16 ng/ml升至47 ng/ml。所有妊娠大鼠的孕酮水平均显著超过雌二醇值,在第14天达到峰值202 ng/ml。妊娠期间孕酮水平升高与LH和雌二醇水平呈负相关。雌二醇水平在第21天显著升高。卵巢免疫组织化学显示,OSE细胞中ERα表达呈阳性染色的水平较低。妊娠第7天和第14天没有ERα阳性细胞,只有第21天记录到OSE细胞核内免疫染色的比例非常低(0.5%)。相反,在所有研究组的OSE细胞核内均未观察到PR的免疫染色。总之,这些结果可能表明,妊娠期间孕酮的作用似乎超过了雌激素对OSE细胞的积极作用。高孕酮水平可能对促性腺激素的产生有直接的负面影响,从而可能抑制导致卵泡发育和OSE增殖的事件。了解影响OSE增殖的因素可能有助于阐明诸如卵巢癌等相关疾病的发病机制。