Wu Yuanyuan, Li Pengfen, Zhang Dan, Sun Yingpu
Reproductive Medicine Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China.
Reproductive Medicine Center, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450014, P.R. China.
Exp Ther Med. 2018 Feb;15(2):2120-2127. doi: 10.3892/etm.2017.5650. Epub 2017 Dec 15.
Polycystic ovary syndrome (PCOS) is a common gynecological endocrine disorder, which results in health problems such as menstrual disorders, hyperandrogenism and persistent anovulation. Hyperandrogenism and insulin resistance are the basic characteristics of PCOS. To investigate the combined effect of metformin and pioglitazone on POCS and the potential mechanisms, a rat model of PCOS was established by intramuscular injection of estradiol valerate (EV). The effect of metformin and pioglitazone monotherapy or combination therapy in control rats and PCOS rats was evaluated, involving the testosterone level, follicular development and insulin resistance. The potential mechanism for the therapeutic effect of metformin and pioglitazone on POCS was explored through using three inhibitors of the 5'adenosine monophosphate-activated protein kinase (AMPK)/phosphoinositide-3 kinase (PI3K)/c-Jun N-terminal kinase (JNK) pathway (Compound C, Wortmannin and SP600125). The results showed that EV-induced PCOS rats demonstrated hyperandrogenemia, hyperinsulinemia and follicular dysplasia. Metformin or pioglitazone monotherapy significantly suppressed the high level of testosterone, reduced the raised percentage of cystic follicles and primary follicles, promoted the number of early antral follicles, and markedly decreased the high concentration of fasting insulin and homeostatic model assessment for insulin resistance index in PCOS rats. In addition, metformin and pioglitazone combination therapy demonstrated greater efficacy than its individual components. Furthermore, individual or joint treatment with metformin and pioglitazone affected the phosphorylation level of JNK in PCOS rats. Compound C and Wortmannin eliminated the effect of metformin and pioglitazone combination therapy on improving the follicular growth in PCOS rats, whereas SP600125 treatment enhanced this combination therapy effect. These data suggested that metformin and pioglitazone combination therapy demonstrated great efficacy in ameliorating PCOS through regulating the AMPK/PI3K/JNK pathway.
多囊卵巢综合征(PCOS)是一种常见的妇科内分泌疾病,会导致月经紊乱、高雄激素血症和持续性无排卵等健康问题。高雄激素血症和胰岛素抵抗是PCOS的基本特征。为了研究二甲双胍和吡格列酮联合应用对PCOS的影响及其潜在机制,通过肌肉注射戊酸雌二醇(EV)建立了PCOS大鼠模型。评估了二甲双胍和吡格列酮单药治疗或联合治疗对对照大鼠和PCOS大鼠的影响,包括睾酮水平、卵泡发育和胰岛素抵抗。通过使用5' - 腺苷单磷酸激活蛋白激酶(AMPK)/磷脂酰肌醇-3激酶(PI3K)/c - Jun氨基末端激酶(JNK)通路的三种抑制剂(化合物C、渥曼青霉素和SP600125),探索了二甲双胍和吡格列酮对PCOS治疗作用的潜在机制。结果显示,EV诱导的PCOS大鼠表现出高雄激素血症、高胰岛素血症和卵泡发育异常。二甲双胍或吡格列酮单药治疗可显著抑制睾酮的高水平,降低囊性卵泡和初级卵泡的升高百分比,促进早期窦卵泡数量增加,并显著降低PCOS大鼠空腹胰岛素的高浓度和胰岛素抵抗指数的稳态模型评估值。此外,二甲双胍和吡格列酮联合治疗的疗效优于其单一成分。此外,二甲双胍和吡格列酮单独或联合治疗会影响PCOS大鼠中JNK的磷酸化水平。化合物C和渥曼青霉素消除了二甲双胍和吡格列酮联合治疗对改善PCOS大鼠卵泡生长的作用,而SP600125治疗增强了这种联合治疗效果。这些数据表明,二甲双胍和吡格列酮联合治疗通过调节AMPK/PI3K/JNK通路在改善PCOS方面具有显著疗效。