Saedi A, Zarei S, Vatanparast M, Hajizadeh M R, Hosseiniara R, Esmaeili O S, Mohammad-Sadeghipour M, Mirzaei Z, Mahmoodi M
Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran; Department of Clinical Biochemistry, Afzalipoor Faculty of Medicine, Kerman University of Medical Sciences, Kerman, Iran.
Department of Clinical Biochemistry, Faculty of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran; Molecular Medicine Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
Ann Pharm Fr. 2025 Mar;83(2):297-310. doi: 10.1016/j.pharma.2024.08.008. Epub 2024 Aug 23.
This study aimed to assess the individual and combined effects of SAE and Met on the expression of genes related to insulin signaling, oxidative stress, hormonal imbalance, insulin resistance, and dyslipidemia in rats with induced PCOS.
The estrous cycle of 50 adult Wistar female rats was monitored through vaginal smears. Subsequently, the rats were randomly assigned into five groups of 10, including control (receiving 1ml of carboxymethyl cellulose for 49 days), induction (letrozole at 1mg/kg/d for 21 days), SAE, Met, and SAE/Met. SAE and Met were orally administered at doses of 400mg/kg/d and 250mg/kg/d on day 22 and continued for an additional 28 days. Vaginal smears were analyzed, and gene expression levels of GLUT4, SIRT1, TNF-α, and INSR were evaluated using RT-qPCR. Antioxidant parameters were assessed using detection kits.
Treatment with SAE and Met restored a regular estrous cycle pattern in PCOS rats. Furthermore, SAE and Met treatment improved hormonal balance, dyslipidemia, and hyperglycemia in the rats. Administration of SAE and Met significantly elevated levels of antioxidant enzymes SOD and GPx in ovarian tissue (P<0.001). Additionally, mRNA levels of GLUT4, SIRT1, and INSR were significantly increased in ovarian tissue following SAE and Met treatment, while TNF-α gene expression decreased significantly (P<0.0001).
The findings suggest that SAE and Met aqueous extract exert protective effects on letrozole-induced PCOS in rats by modulating gene expression associated with insulin signaling and oxidative stress.
本研究旨在评估南非叶(SAE)和二甲双胍(Met)对诱导性多囊卵巢综合征(PCOS)大鼠胰岛素信号、氧化应激、激素失衡、胰岛素抵抗和血脂异常相关基因表达的个体及联合作用。
通过阴道涂片监测50只成年Wistar雌性大鼠的发情周期。随后,将大鼠随机分为五组,每组10只,包括对照组(接受1ml羧甲基纤维素,持续49天)、诱导组(来曲唑1mg/kg/d,持续21天)、SAE组、Met组和SAE/Met组。SAE和Met于第22天开始以400mg/kg/d和250mg/kg/d的剂量口服给药,并持续额外28天。分析阴道涂片,并使用RT-qPCR评估GLUT4、SIRT1、TNF-α和INSR的基因表达水平。使用检测试剂盒评估抗氧化参数。
SAE和Met治疗恢复了PCOS大鼠的正常发情周期模式。此外,SAE和Met治疗改善了大鼠的激素平衡、血脂异常和高血糖。SAE和Met给药显著提高了卵巢组织中抗氧化酶超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx)的水平(P<0.001)。此外,SAE和Met治疗后卵巢组织中GLUT4、SIRT1和INSR的mRNA水平显著升高,而TNF-α基因表达显著降低(P<0.0001)。
研究结果表明,SAE和Met水提取物通过调节与胰岛素信号和氧化应激相关的基因表达,对来曲唑诱导的大鼠PCOS发挥保护作用。