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新型硒纳米粒子与二甲双胍联合治疗来曲唑诱导多囊卵巢综合征的协同作用机制研究:靶向作用于卵巢组织中 PI3K/Akt 信号通路、氧化还原状态和线粒体功能障碍。

Novel insights into the synergistic effects of selenium nanoparticles and metformin treatment of letrozole - induced polycystic ovarian syndrome: targeting PI3K/Akt signalling pathway, redox status and mitochondrial dysfunction in ovarian tissue.

机构信息

Medical Biochemistry Department, Faculty of Medicine, Tanta University, Tanta, Egypt.

Histopathology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.

出版信息

Redox Rep. 2023 Dec;28(1):2160569. doi: 10.1080/13510002.2022.2160569.

Abstract

PURPOSE

Polycystic ovary syndrome (PCOS) has a series of reproductive and metabolic consequences. Although the link between PCOS, IR, and obesity, their impact on the pathogenesis of PCOS has yet to be determined. Dysfunction of PI3K/AKT pathway has been reported as the main cause of IR in PCOS. This study purposed to explore the effects of selenium nanoparticles (SeNPs) alone and combined with metformin (MET) in a PCOS-IR rat model.

METHODS

After 3 weeks of treatment with SeNPs and/or MET, biochemical analysis of glycemic & lipid profiles, and serum reproductive hormones was performed. Inflammatory, oxidative stress, and mitochondrial dysfunction markers were determined colormetrically. The expression of PI3K and Akt genes were evaluated by Real-time PCR. Histopathological examination and Immunohistochemical analysis of Ki-67 expression were performed.

RESULTS

The results showed that treatment with SeNPs and/or MET significantly attenuated insulin sensitivity, lipid profile, sex hormones levels, inflammatory, oxidative stress and mitochondrial functions markers. Additionally, PI3K and Akt genes expression were significantly upregulated with improved ovarian histopathological changes.

CONCLUSION

Combined SeNPs and MET therapy could be potential therapeutic agent for PCOS-IR model via modulation of the PI3K/Akt pathway, enhancing anti-inflammatory and anti-oxidant properties and altered mitochondrial functions.

UNLABELLED

HighlightsThe strong relationship between obesity, insulin resistance, and polycystic ovarian syndrome.Disturbance of the PI3K/Akt signaling pathway is involved in the progression of polycystic ovary syndrome-insulin resistance (PCOS-IR).In PCOS-IR rats, combined SeNPs and metformin therapy considerably alleviated IR by acting on the PI3K/Akt signaling pathway.The combination of SeNPs and metformin clearly repaired ovarian polycystic pathogenesis and improved hormonal imbalance in PCOS-IR rats.

摘要

目的

多囊卵巢综合征(PCOS)具有一系列生殖和代谢后果。虽然 PCOS、IR 和肥胖之间存在联系,但它们对 PCOS 发病机制的影响尚未确定。PI3K/AKT 通路功能障碍已被报道为 PCOS 中 IR 的主要原因。本研究旨在探讨硒纳米粒子(SeNPs)单独和与二甲双胍(MET)联合应用于 PCOS-IR 大鼠模型的效果。

方法

用 SeNPs 和/或 MET 处理 3 周后,进行血糖和血脂谱的生化分析以及血清生殖激素分析。比色法测定炎症、氧化应激和线粒体功能障碍标志物。通过实时 PCR 评估 PI3K 和 Akt 基因的表达。进行组织病理学检查和 Ki-67 表达的免疫组织化学分析。

结果

结果表明,用 SeNPs 和/或 MET 处理可显著改善胰岛素敏感性、脂质谱、性激素水平、炎症、氧化应激和线粒体功能障碍标志物。此外,PI3K 和 Akt 基因表达显著上调,卵巢组织病理学变化得到改善。

结论

联合 SeNPs 和 MET 治疗可能通过调节 PI3K/Akt 通路成为 PCOS-IR 模型的潜在治疗剂,增强抗炎和抗氧化特性并改变线粒体功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3266/9870018/9c1b7338a994/YRER_A_2160569_F0001_OC.jpg

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