Wang Rongrong, Wang Qian, Liu Mingfei, Xiao He, Zhang Guimin, Yao Jingchun, Liu Ming
Key Laboratory of Marine Drugs, Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, People's Republic of China.
Laboratory for Marine Drugs and Bioproducts, Qingdao Marine Science and Technology Center, Qingdao, 266237, People's Republic of China.
Drug Des Devel Ther. 2025 Jun 4;19:4835-4860. doi: 10.2147/DDDT.S516298. eCollection 2025.
Diabetic wounds are one of the most common complications of diabetes mellitus. Jingfang Granules (JFG), a combination of 11 herbs, has been clinically used for treating colds and the flu and for preventing various skin diseases.
The present study was designed to evaluate the therapeutic effect of JFG on diabetic wounds and to elucidate the associated mechanisms.
JFG serum was prepared using Sprague-Dawley rats and the phytochemicals of JFG in the serum were identified using UHPLC-ESI-QE-Orbitrap-MS. A cell viability assay and cellular angiogenesis methods were performed to evaluate wound healing in vitro. Diabetic wounds were developed using streptozotocin-induced diabetic rats to investigate the efficacy of JFG on diabetic wounds in vivo. Network pharmacology analysis, molecular docking, and Western blot were performed to elucidate the potential mechanisms of JFG in diabetic wound healing.
JFG serum attenuated HO-induced and high glucose-induced oxidative damage, significantly reduced lipopolysaccharide-induced upregulation of inflammatory cytokines, and promoted angiogenesis in vitro. In diabetic rats, JFG effectively promoted wound healing, reduced blood glucose and lipid levels, and alleviated oxidative stress and inflammation. A total of 56 phytochemicals were identified in the JFG serum. Six core targets (AKT1, EGFR, MAPK3, MAPK1, IL6, and TNF) and the PI3K-AKT and MAPK signaling pathways were identified by network pharmacology analysis, which were further validated by subsequent experimental methods.
JFG could accelerate diabetic wound healing by alleviating oxidative damage, suppressing inflammation, promoting angiogenesis, and regulating metabolic abnormalities, with involvement of the PI3K-AKT and MAPK signaling pathways.
糖尿病伤口是糖尿病最常见的并发症之一。荆防颗粒(JFG)由11味草药组成,已在临床上用于治疗感冒和流感以及预防各种皮肤病。
本研究旨在评估JFG对糖尿病伤口的治疗效果并阐明其相关机制。
使用Sprague-Dawley大鼠制备JFG血清,并采用超高效液相色谱-电喷雾电离-四级杆-轨道阱质谱法(UHPLC-ESI-QE-Orbitrap-MS)鉴定血清中JFG的植物化学成分。进行细胞活力测定和细胞血管生成方法以评估体外伤口愈合情况。使用链脲佐菌素诱导的糖尿病大鼠建立糖尿病伤口模型,以研究JFG对体内糖尿病伤口的疗效。进行网络药理学分析、分子对接和蛋白质免疫印迹法以阐明JFG在糖尿病伤口愈合中的潜在机制。
JFG血清减轻了过氧化氢(HO)诱导的和高糖诱导的氧化损伤,显著降低了脂多糖诱导的炎症细胞因子上调,并在体外促进了血管生成。在糖尿病大鼠中,JFG有效促进伤口愈合,降低血糖和血脂水平,并减轻氧化应激和炎症。在JFG血清中总共鉴定出56种植物化学成分。通过网络药理学分析确定了六个核心靶点(AKT1、表皮生长因子受体(EGFR)、丝裂原活化蛋白激酶3(MAPK3)、丝裂原活化蛋白激酶1(MAPK1)、白细胞介素6(IL6)和肿瘤坏死因子(TNF))以及磷脂酰肌醇-3激酶-蛋白激酶B(PI3K-AKT)和丝裂原活化蛋白激酶(MAPK)信号通路,随后的实验方法进一步验证了这些结果。
JFG可通过减轻氧化损伤、抑制炎症、促进血管生成和调节代谢异常来加速糖尿病伤口愈合,PI3K-AKT和MAPK信号通路参与其中。