Li Panpan, Xiao Cenyu, Lv Zhiyuan, Cui Haiyang, Gao Xiaoli
College of Pharmacy, Xinjiang Medical University, Urumqi 830011, China.
Xinjiang Key Laboratory of Active Components and Drug Release Technology of Natural Drugs, Urumqi 830011, China.
Biomedicines. 2024 Sep 11;12(9):2074. doi: 10.3390/biomedicines12092074.
The purpose of this study was to investigate the impact of conjugated estrogen cream, in conjunction with progesterone, on the endometrium, following vaginal administration, and assess the combined dose-effect relationship with progesterone. Initially, bilateral ovaries from mature, female, Sprague Dawley rats were excised to establish a hypoestrogenic (perimenopausal) model. A conjugated estrogen-progesterone combination cream was administered vaginally for a duration of 12 days. Subsequently, this study used pathological sections, Enzyme-Linked Immunosorbent Assay (ELISA) for pharmacodynamic studies, network pharmacology to explore possible signalling pathways associated with the drug and menopausal syndrome, and partial validation using a real-time quantitative polymerase chain reaction (RT-qPCR) and immunohistochemistry (ICH). The results demonstrate that, relative to the model group, the conjugated estrogen monotherapy significantly increased the uterine weight coefficients ( < 0.0001) and endometrial thickness ( < 0.001) and upregulated the expression of Cyclin D1 and VEGF. Moreover, this treatment downregulated PTEN expression. The co-administration of progesterone reversed these effects in a dose-dependent manner. Overall, the vaginal administration of a combination of progesterone and conjugated estrogen cream demonstrated the ability to mitigate endometrial hyperplasia induced by conjugated estrogen vaginal cream monotherapy. Furthermore, the effect of progesterone exhibited a dose-dependent response.
本研究的目的是探讨结合雌激素乳膏联合孕激素经阴道给药后对子宫内膜的影响,并评估其与孕激素的联合剂量效应关系。最初,切除成熟雌性Sprague Dawley大鼠的双侧卵巢以建立低雌激素(围绝经期)模型。经阴道给予结合雌激素 - 孕激素组合乳膏,持续12天。随后,本研究采用病理切片、酶联免疫吸附测定(ELISA)进行药效学研究,利用网络药理学探索与药物和绝经综合征相关的可能信号通路,并通过实时定量聚合酶链反应(RT-qPCR)和免疫组织化学(ICH)进行部分验证。结果表明,相对于模型组,单纯使用结合雌激素显著增加子宫重量系数(<0.0001)和子宫内膜厚度(<0.001),并上调细胞周期蛋白D1和血管内皮生长因子(VEGF)的表达。此外,该治疗下调了磷酸酶和张力蛋白同源物(PTEN)的表达。孕激素的联合使用以剂量依赖性方式逆转了这些作用。总体而言,经阴道给予孕激素和结合雌激素乳膏的组合显示出减轻结合雌激素阴道乳膏单一疗法引起的子宫内膜增生的能力。此外,孕激素的作用表现出剂量依赖性反应。