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桑枝生物碱通过 NRF2/HO-1/eNOS 通路加速糖尿病创面愈合。

Accelerating diabetic wound healing with Ramulus Mori (Sangzhi) alkaloids via NRF2/HO-1/eNOS pathway.

机构信息

Department of Endocrinology and Metabolism, School of Medicine, Chongqing University Central Hospital, Chongqing Emergency Medical Centre, Chongqing University, Chongqing 400014, China.

Department of Traumatology, Chongqing University Central Hospital, Chongqing Emergency Medical Center, Chongqing University, Chongqing 400014, China.

出版信息

Phytomedicine. 2024 Nov;134:155990. doi: 10.1016/j.phymed.2024.155990. Epub 2024 Aug 31.

Abstract

Diabetic foot ulcers (DFUs) represent a severe complication of diabetes mellitus. Ramulus Mori (Sangzhi) alkaloids (SZ-A), an approved oral medication for type 2 diabetes, have not been explored for their potential to enhance the processes involved in diabetic wound healing. This study aims to investigate SZ-A's role in diabetic wound healing mechanisms. The in vivo experimentation involves dividing the subjects into NC and SZ-A groups, with SZ-A dosed at 200 and 400 mg/kg, to assess the therapeutic efficacy of SZ-A. The results of the animal studies show that SZ-A intervention accelerates the processes of diabetic angiogenesis and wound healing in a manner dependent on its concentration. Additionally, a pathological model using advanced glycation end products (AGEs) in HUVECs demonstrates SZ-A's cytoprotective effect. In vitro, SZ-A intervention significantly increases cell proliferation, migration and tube formation, protecting HUVECs from oxidative stress injury induced by AGEs. Mechanistically, SZ-A exerts a protective effect on HUVECs from oxidative stress damage through the activation of the NRF2/HO-1/eNOS signaling pathway. The findings suggest that SZ-A exhibits considerable potential as a promising candidate for treating DFUs, which will aid in more effectively integrating plant-based therapies into clinical settings.

摘要

桑树桑枝生物碱(SZ-A)是一种已批准用于治疗 2 型糖尿病的口服药物,尚未探索其在促进糖尿病伤口愈合过程中的潜在作用。本研究旨在探讨 SZ-A 在糖尿病伤口愈合机制中的作用。体内实验将研究对象分为 NC 和 SZ-A 组,SZ-A 剂量为 200 和 400mg/kg,以评估 SZ-A 的治疗效果。动物研究结果表明,SZ-A 干预可加速糖尿病血管生成和伤口愈合过程,且这种作用与 SZ-A 的浓度有关。此外,在使用晚期糖基化终产物(AGEs)的 HUVECs 病理模型中,SZ-A 具有细胞保护作用。体外实验表明,SZ-A 干预可显著增加细胞增殖、迁移和管形成,保护 HUVECs 免受 AGEs 诱导的氧化应激损伤。从机制上讲,SZ-A 通过激活 NRF2/HO-1/eNOS 信号通路对 HUVECs 的氧化应激损伤发挥保护作用。这些发现表明,SZ-A 作为治疗糖尿病足溃疡的有前途的候选药物具有很大的潜力,这将有助于更有效地将植物疗法整合到临床实践中。

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