20(R)-ginsenoside Rg3 alleviates diabetic retinal injury in T2DM mice by attenuating ROS-mediated ER stress through the activation of the Nrf2/HO-1 axis.

IF 6.7 1区 医学 Q1 CHEMISTRY, MEDICINAL
Wen-Lin Li, Ke Li, Wen-Guang Chang, Hui Shi, Wen-Xuan Zhang, Zi Wang, Wei Li
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引用次数: 0

Abstract

Background: Although our previous work confirmed 20(R)-ginsenoside Rg3 (R-Rg3), which is an active ingredient in the Panax Ginseng C.A. Meyer, to have good anti-diabetic activity, its beneficial effect on diabetic retinal injury was found to be limited.

Purpose: This study aims to investigate the protective effects of R-Rg3 on diabetes-induced retinal injury and the associated molecular mechanisms of action.

Methods: Diabetic retinal injury was induced in mice using a combination of a high-fat diet (HFD) and intraperitoneal injection of streptozotocin (STZ). R-Rg3 (10 and 20 mg/kg) was subsequently administered for 6 weeks. The human retinal endothelial cells (HRECs) were subjected to high glucose (HG)-induced injury for the in vitro analysis and treated with R-Rg3 (4, 8, 16 μM), antioxidant N-Acetylcysteine (NAC, 1 mM) and Nrf2 inhibitor ML385 (5 μM). The mice retinas then underwent functional and histopathological analysis. Expression levels of proteins related to the Nrf2/HO-1 axis, tight junction proteins, endoplasmic reticulum (ER) stress and the apoptosis in retinal tissue and HRECs were determined by western blot. Expressions of ZO-1 and Nrf2 in the retina and HRECs were assessed by immunofluorescence. Additional evaluations included measuring body weights, fasting blood glucose (FBG), lipid levels and oxidative markers.

Results: The results showed 6 weeks of R-Rg3 treatment significantly restored the functional changes and redox system imbalance that was induced by HFD/STZ in mice. R-Rg3 was also found to significantly reduce retinal barrier damage and thickness changes resulting from hyperglycaemia exposure. At the same time, R-Rg3 also protected HRECs from HG-induced damage. R-Rg3 could also activate Nrf2/HO-1 axis and inhibit endoplasmic reticulum stress as a means of alleviating retinal endothelial cells apoptosis. The molecular docking results also demonstrated that R-Rg3 had a good binding ability with Nrf2.

Conclusion: Our study suggested Nrf2/HO-1 axis might be crucial for the ability of R-Rg3 to prevent diabetic retinal injury.

20(R)-人参皂苷Rg3通过激活Nrf2/HO-1轴减轻ROS介导的ER应激,从而减轻T2DM小鼠的糖尿病视网膜损伤。
背景:目的:本研究旨在探讨20(R)-人参皂苷Rg3(R-Rg3)对糖尿病引起的视网膜损伤的保护作用及其相关的分子作用机制:方法:采用高脂饮食(HFD)和腹腔注射链脲佐菌素(STZ)联合诱导小鼠糖尿病视网膜损伤。随后连续 6 周给小鼠注射 R-Rg3(10 和 20 毫克/千克)。在体外分析中,人视网膜内皮细胞(HRECs)受到高糖(HG)诱导的损伤,并接受 R-Rg3(4、8、16 μM)、抗氧化剂 N-乙酰半胱氨酸(NAC,1 mM)和 Nrf2 抑制剂 ML385(5 μM)的治疗。然后对小鼠视网膜进行功能和组织病理学分析。用 Western 印迹法测定视网膜组织和 HRECs 中与 Nrf2/HO-1 轴、紧密连接蛋白、内质网(ER)应激和细胞凋亡有关的蛋白质的表达水平。视网膜和 HRECs 中 ZO-1 和 Nrf2 的表达通过免疫荧光进行评估。其他评估包括测量体重、空腹血糖(FBG)、血脂水平和氧化标记物:结果:结果表明,6 周的 R-Rg3 治疗可明显恢复小鼠因高密度脂蛋白胆固醇(HFD)/STZ 引起的功能变化和氧化还原系统失衡。研究还发现,R-Rg3 能明显减少高血糖导致的视网膜屏障损伤和厚度变化。同时,R-Rg3 还能保护 HRECs 免受 HG 引起的损伤。R-Rg3 还能激活 Nrf2/HO-1 轴,抑制内质网应激,从而缓解视网膜内皮细胞凋亡。分子对接结果还表明,R-Rg3 与 Nrf2 具有良好的结合能力:我们的研究表明,Nrf2/HO-1轴可能是R-Rg3预防糖尿病视网膜损伤的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Phytomedicine
Phytomedicine 医学-药学
CiteScore
10.30
自引率
5.10%
发文量
670
审稿时长
91 days
期刊介绍: Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.
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