Golkar Mohammad Hosein, Saeedi Borujeni Mohammad Javad, Rashidi Bahman
Student Research Center, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Molecular Biology and Anatomical Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Adv Biomed Res. 2017 Dec 26;6:164. doi: 10.4103/abr.abr_79_17. eCollection 2017.
Ovarian angiogenesis (OA) remains in lifetime and normal ovarian function depends to this continual remodeling of a complex vascular system. Endometrial thickness (ET) is one of the strongest predictors of successful implantation and pregnancy. Appropriate OA effects on ET by facilitating of ovarian hormone delivery.
Thirty adult female mice and twenty adult male mice were purchased. The female mice were divided into three groups: (1) control group without any intervention ( = 10), (2) gonadotropin group: receiving human menopausal gonadotropin (HMG) and human chorionic gonadotropin ( = 10), and (3) gonadotropin and sildenafil citrate (SC) group: receiving HMG and SC administration ( = 10). After mating, animals were deeply anesthetized, and the ovary and uterus was rapidly removed for histology and immunohistochemistry process.
Four days after ovarian induction, all three layers of the uterus with specified thickness can be clearly seen. The heights of endometrial epithelial cells in gonadotropin group were not significantly different than those in control group. In gonadotropin and SC group, heights of the cells were significantly ( < 0.05) shorter than control and gonadotropin groups. ETs in all groups were not significantly deferent from each other ( > 0.05 each). Our results of immunohistochemistry survey for ovarian CD31 demonstrated that administrated SC increased OA but not significantly ( > 0.05 each).
It may finally conclude that administration of SC does not cause notable alterations in OA and ET; although for realistic decision about the SC effects on aforementioned parameters, more molecular investigations and longer drug consumption period are necessary.
卵巢血管生成(OA)持续终生,正常卵巢功能依赖于这一复杂血管系统的持续重塑。子宫内膜厚度(ET)是成功着床和妊娠的最强预测指标之一。适当的OA通过促进卵巢激素输送对ET产生影响。
购买30只成年雌性小鼠和20只成年雄性小鼠。将雌性小鼠分为三组:(1)无任何干预的对照组(n = 10),(2)促性腺激素组:接受人绝经期促性腺激素(HMG)和人绒毛膜促性腺激素(n = 10),以及(3)促性腺激素和枸橼酸西地那非(SC)组:接受HMG和SC给药(n = 10)。交配后,将动物深度麻醉,迅速取出卵巢和子宫进行组织学和免疫组织化学处理。
卵巢诱导4天后,可清晰看到具有特定厚度的子宫三层结构。促性腺激素组子宫内膜上皮细胞高度与对照组无显著差异。在促性腺激素和SC组中,细胞高度显著低于对照组和促性腺激素组(P < 0.05)。各组ET之间无显著差异(每组P > 0.05)。我们对卵巢CD31的免疫组织化学检测结果表明,给予SC可增加OA,但不显著(每组P > 0.05)。
最终可以得出结论,给予SC不会引起OA和ET的显著改变;尽管要对SC对上述参数的影响做出实际决策,还需要更多的分子研究和更长的药物服用期。