Rashidi Bahman, Mardani Mohammad, Karizbodagh Mostafa Peyvandi
Department of Anatomical Sciences and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Anatomical Sciences and Molecular Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Adv Biomed Res. 2017 Sep 21;6:116. doi: 10.4103/abr.abr_179_16. eCollection 2017.
Human endometrium is a dynamic tissue during the menstrual cycle can be influenced by ovarian hormones. The purpose of this study was to evaluate the endometrium angiogenesis under the influence of human menopausal gonadotropin and human chorionic gonadotropin (HMG and HCG) that stimulate ovulation and progesterone.
In this study, thirty adult female mice were randomly divided into three groups as: control, gonadotropin and gonadotropin + progesterone. The mice in the other two groups except the control group received 7.5 IU HMG and later HCG. Subsequently, the mice were placed in a cage for mating. Gonadotropin + progesterone group was administered, 1 mg/mouse progesterone in 24, 48, and 72 h interval, after HMG injection. Ninety-six hours after HMG injection, animals were sacrificed, and their uterine specimens were prepared by immunohistochemistry technique for light microscopic studies, and statistical analysis was carried out.
Endometrium angiogenesis in control group showed that mean ± standard deviation was 24.15 ± 11.15, gonadotropin group was 62.50 ± 24.16, and gonadotropin + progesterone group was 41.85 ± 19.54. Significant difference between the control group and gonadotropin group and between the control group and gonadotropin + progesterone was observed. Statistically significant differences were observed in all groups in the endometrial angiogenesis ( < 0.05).
Ovarian induction with gonadotropins and gonadotropins + progesterone could not change the morphometrically index of endometrial glandular epithelium in mice. Ovarian stimulation followed by progesterone injection could modify the angiogenesis of mice endometrium.
人类子宫内膜是月经周期中的动态组织,会受到卵巢激素的影响。本研究的目的是评估在刺激排卵的人绝经期促性腺激素和人绒毛膜促性腺激素(HMG和HCG)以及孕酮影响下的子宫内膜血管生成情况。
在本研究中,30只成年雌性小鼠被随机分为三组:对照组、促性腺激素组和促性腺激素+孕酮组。除对照组外,其他两组小鼠接受7.5国际单位的HMG,随后接受HCG。随后,将小鼠放入笼中进行交配。促性腺激素+孕酮组在注射HMG后,每隔24、48和72小时给每只小鼠注射1毫克孕酮。注射HMG 96小时后,处死动物,通过免疫组织化学技术制备子宫标本用于光学显微镜研究,并进行统计分析。
对照组子宫内膜血管生成情况显示,平均值±标准差为24.15±11.15,促性腺激素组为62.50±24.16,促性腺激素+孕酮组为41.85±19.54。观察到对照组与促性腺激素组之间以及对照组与促性腺激素+孕酮组之间存在显著差异。在所有组的子宫内膜血管生成中均观察到统计学上的显著差异(<0.05)。
用促性腺激素以及促性腺激素+孕酮进行卵巢诱导不能改变小鼠子宫内膜腺上皮的形态学指标。卵巢刺激后注射孕酮可改变小鼠子宫内膜的血管生成。