氢处理通过抑制皮肤细胞AGEs/RAGE/NF-κB信号通路对高糖诱导的氧化应激和凋亡的保护作用

Pan Yu, Nan Hong, Qiong Wu, Zhipeng Zhao
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引用次数: 0

摘要

背景:糖尿病性伤口是临床面临的主要挑战,通常伴有氧化应激和自由基的产生。氢(H2)是一种选择性抗氧化剂,具有治疗慢性糖尿病伤口的潜力。然而,其确切机制仍未得到充分探索。目的:探讨H2对高糖诱导的皮肤细胞氧化损伤和凋亡的保护作用。方法:采用高糖或AGEs处理HaCaT角质形成细胞和HSF成纤维细胞。分析细胞活力、氧化应激标志物、炎症因子和细胞凋亡。Western blot检测AGEs/RAGE/NF-κB信号通路。结果:H2处理显著降低ROS、MDA、IL-1β、TNF-α水平,提高SOD和GSH活性。抑制AGEs/RAGE/NF-κB信号通路及细胞凋亡。结论:氢疗法对高糖或AGEs诱导的氧化应激和炎症有保护作用,有可能作为糖尿病伤口愈合的辅助治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective Effects of Hydrogen Treatment Against High Glucose-Induced Oxidative Stress and Apoptosis via Inhibition of the AGEs/RAGE/NF-κB Signaling Pathway in Skin Cells.

Background: Diabetic wounds are major clinical challenges, often complicated by oxidative stress and free radical generation. Hydrogen (H2), a selective antioxidant, offers potential as a therapeutic agent for chronic diabetic wounds. However, its precise mechanisms remain underexplored.

Objective: This study aimed to investigate the protective effects of H2 on high glucose-induced oxidative damage and apoptosis in human skin cells.

Methods: HaCaT keratinocytes and HSF fibroblasts were treated with high glucose or AGEs. Cell viability, oxidative stress markers, inflammatory cytokines, and apoptosis were analyzed. AGEs/RAGE/NF-κB signaling was evaluated via Western blot.

Results: H2 treatment significantly reduced ROS, MDA, IL-1β, and TNF-α levels, while enhancing SOD and GSH activity. It also inhibited AGEs/RAGE/NF-κB signaling and apoptosis.

Conclusion: Hydrogen therapy protects against oxidative stress and inflammation induced by high glucose or AGEs, offering potential as an adjunctive treatment for diabetic wound healing.

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