消罗丸治疗甲状腺相关性眼病的分子机制研究:网络分析和体内研究。

IF 2.5 3区 生物学
Wenchao Gu, Shuo Tian, Lu Fu, Lina Wang, Liangkun Zhang, Furong Wang
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引用次数: 0

摘要

背景:甲状腺相关性眼病(TAO)是甲状腺功能亢进的常见并发症,可显著影响生活质量。本研究探讨中药消络丸治疗TAO的作用及机制。方法:首次观察XLW对甲状腺功能亢进大鼠眼外肌保护作用。应用网络分析策略预测与XLW相关的潜在靶点和治疗机制。随后在甲状腺功能亢进大鼠中验证并分析了关键基因和蛋白的表达。结果:XLW能减轻甲状腺机能亢进引起的眼外肌病变。网络分析确定了66个有效目标。XLW抗TAO的核心靶点包括AKT1、PTGS2、BCL2、IL10、IL1b、CCL2、IFNG、IL6、MMP9、TGFB1、HIF1α和TP53。富集分析表明XLW的改善机制可能与HIF1信号通路有关。在甲状腺功能亢进大鼠中,XLW可降低眼外肌氧化应激(OS),抑制HIF-1的表达。此外,XLW对HIF-1α和OS密切相关的多种蛋白的表达具有调节作用。结论:XLW可能通过HIF1信号抑制OS,从而减轻甲亢患者眼外肌损伤。这可能为XLW治疗TAO的药理机制提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of the molecular mechanism of Xiaoluo Wan in thyroid-associated ophthalmopathy: network analysis and in vivo study.

Background: Thyroid-associated ophthalmopathy (TAO) is a common complication of hyperthyroidism that can significantly impair quality of life. This study investigated the effects and mechanisms of Xiaoluo Wan (XLW), a traditional Chinese herbal prescription, in treating TAO.

Methods: The protective effects of XLW on the extraocular muscles were first examined in hyperthyroid rats. Network analysis strategies were applied to predict potential targets and therapeutic mechanisms associated with XLW. The expression of key genes and proteins was subsequently validated and analyzed in rats with hyperthyroidism.

Results: XLW alleviated the pathological changes in the extraocular muscles caused by hyperthyroidism. The network analysis identified 66 effective targets. The core targets of XLW against TAO included AKT1, PTGS2, BCL2, IL10, IL1b, CCL2, IFNG, IL6, MMP9, TGFB1, HIF1α, and TP53. Enrichment analysis suggested that the amelioration mechanisms of XLW may be linked to the HIF1 signaling pathway. In hyperthyroid rats, XLW reduced oxidative stress (OS) in extraocular muscle and inhibited the expression of HIF-1ɑ. Additionally, XLW exerted regulatory actions on the expression of various proteins closely linked to HIF-1α and OS.

Conclusions: XLW reduces injuries to extraocular muscles in hyperthyroidism, possibly by inhibiting OS via HIF1 signaling. This may provide novel insights into the pharmacological mechanism of XLW in treating TAO.

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来源期刊
Hereditas
Hereditas Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.80
自引率
3.70%
发文量
0
期刊介绍: For almost a century, Hereditas has published original cutting-edge research and reviews. As the Official journal of the Mendelian Society of Lund, the journal welcomes research from across all areas of genetics and genomics. Topics of interest include human and medical genetics, animal and plant genetics, microbial genetics, agriculture and bioinformatics.
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