Gu Wenchao, Tian Shuo, Fu Lu, Wang Lina, Zhang Liangkun, Wang Furong
College of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, 250355, China.
Medical College, Shandong University of Traditional Chinese Medicine, Jinan, 250355, China.
Hereditas. 2025 Jul 22;162(1):137. doi: 10.1186/s41065-025-00499-0.
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.
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.
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.
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.
甲状腺相关眼病(TAO)是甲状腺功能亢进症的常见并发症,可显著损害生活质量。本研究探讨了中药方剂消瘰丸(XLW)治疗TAO的效果及机制。
首先在甲状腺功能亢进大鼠中检测XLW对眼外肌的保护作用。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关键基因和蛋白质的表达。
XLW减轻了甲状腺功能亢进引起的眼外肌病理变化。网络分析确定了66个有效靶点。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降低了眼外肌的氧化应激(OS),并抑制了HIF-1ɑ的表达。此外,XLW对与HIF-1α和OS密切相关的各种蛋白质的表达具有调节作用。
XLW可能通过HIF1信号通路抑制OS,从而减轻甲状腺功能亢进症对眼外肌的损伤。这可能为XLW治疗TAO的药理机制提供新的见解。