JOURNAL OF SHANDONG UNIVERSITY(NATURAL SCIENCE) ›› 2025, Vol. 60 ›› Issue (9): 31-40.doi: 10.6040/j.issn.1671-9352.0.2025.031

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Mechanism of Resina Draconis in promoting healing of diabetic foot wounds

YANG Ziyu, DAI Zhaoyuan, LI Gen*, FENG Xinchi   

  1. School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China
  • Published:2025-09-10

Abstract: Network pharmacology, molecular docking, and experimental verification were employed to investigate the mechanism by which Resina Draconis promotes the healing of diabetic foot wounds. The TCMSP database was utilized to screen the chemical constituents and targets of Resina Draconis. Disease targets were retrieved from the GeneCards and DisGeNET databases using keywords such as “diabetic foot ulcer” and “diabetic wound”. A “component-disease-target” network diagram was created using the intersections of component targets and disease targets. Bioinformatic analysis predicted the mechanism of Resina Draconis in facilitating wound healing. Molecular docking was used to investigate the combination of the components of Resina Draconis and key targets. Mouse macrophages were used to study the effects of Resina Draconis and its main components on the expression of the receptor of advanced glycation end products(RAGE)protein. The results showed that 226 common disease targets were obtained by network pharmacological screening. KEGG enrichment analysis suggested that the effect of Resina Draconis on diabetic ulcers may be associated with the AGE-RAGE pathway. The results of molecular docking demonstrated that loureirin A, loureirin B, loureirin C, loureirin D, resveratrol, and 7,4'-dihydroxyflavone exhibited good binding activity with the key target RAGE. Resina Draconis and its main components could significantly reverse the abnormal expression of RAGE protein in mouse macrophages induced by advanced glycation end products(AGEs). In conclusion, the mechanism of Resina Draconis in promoting healing of diabetic foot ulcers was associated with the regulation of the AGE-RAGE pathway and the inhibition of the abnormal expression of the RAGE protein caused by the accumulation of advanced glycation end products(AGEs).

Key words: Resina Draconis, diabetic foot, network pharmacology, molecular docking, RAGE

CLC Number: 

  • R285
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