Department of Clinical Pharmacy and Pharmacotherapeutics, Dubai Pharmacy College for Girls, Dubai, 19099, United Arab Emirates.
Dubai Pharmacy College for Girls, Dubai, 19099, United Arab Emirates.
Eur J Pharmacol. 2023 Dec 5;960:176119. doi: 10.1016/j.ejphar.2023.176119. Epub 2023 Oct 16.
Polycystic ovary syndrome (PCOS) is a prevalent hormonal disorder that affects women of reproductive age. It is characterized by abnormal production of androgens, typically present in small quantities in females. This study aimed to investigate the therapeutic potential of Irosustat (STX64), STX140, and compound 1G as new drug candidates for the treatment of letrozole-induced PCOS in female Wistar rats. 36 rats were divided into six groups of equal size. PCOS was induced in all groups, except the normal control group, by administering letrozole orally (1 mg/kg/day for 35 days). The onset of abnormal estrous cycle was confirmed by examining daily vaginal smears under a microscope. Subsequently, each rat group was assigned to a different treatment regimen, including one control group, one letrozole group, one metformin group (500 mg/kg/day) as a reference drug, and the other groups received a different drug candidate orally for 30 days. After treatment, blood collection was performed for biochemical measurements and determination of oxidative stress markers. The rats were dissected to separate ovaries and uterus for morphological, histological, and western blotting studies. Treatment with the drug candidates improved the ovaries and uterus weight measurements compared to the untreated PCOS group. The three tested drug candidates demonstrated promising improvements in lipid profile, blood glucose level, testosterone, progesterone, luteinizing hormone (LH), follicle-stimulating hormone (FSH), and estradiol levels. In addition, western blotting confirmed their promising effects on Akt, mTOR, and AMPK-α pathways. This study led to the discovery of three promising drug candidates for the management of PCOS as alternatives to metformin.
多囊卵巢综合征(PCOS)是一种常见的激素紊乱疾病,影响育龄妇女。其特征是雄激素的异常产生,雄激素通常在女性中少量存在。本研究旨在探讨 Irosustat(STX64)、STX140 和化合物 1G 作为治疗来曲唑诱导的雌性 Wistar 大鼠 PCOS 的新药候选物的治疗潜力。36 只大鼠被分为 6 组,每组大小相等。除正常对照组外,所有组均通过口服来曲唑(1mg/kg/天,共 35 天)诱导 PCOS。通过在显微镜下每天检查阴道涂片来确认异常发情周期的发生。随后,每组大鼠被分配到不同的治疗方案,包括一个对照组、一个来曲唑组、一个二甲双胍组(500mg/kg/天)作为参考药物,以及其他组口服不同的药物候选物 30 天。治疗后,采集血液进行生化测量和氧化应激标志物的测定。对大鼠进行解剖以分离卵巢和子宫,进行形态学、组织学和 Western blot 研究。与未治疗的 PCOS 组相比,药物候选物的治疗改善了卵巢和子宫重量的测量值。三种测试的药物候选物在改善血脂谱、血糖水平、睾酮、孕酮、促黄体生成素(LH)、卵泡刺激素(FSH)和雌二醇水平方面表现出良好的效果。此外,Western blot 证实了它们对 Akt、mTOR 和 AMPK-α 途径的有希望的作用。这项研究发现了三种有希望的药物候选物,可作为二甲双胍的替代品用于治疗 PCOS。