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©The Author(s) 2025.
World J Diabetes. Apr 15, 2025; 16(4): 101916
Published online Apr 15, 2025. doi: 10.4239/wjd.v16.i4.101916
Published online Apr 15, 2025. doi: 10.4239/wjd.v16.i4.101916
Figure 7 Molecular docking analysis and mRNA expression analysis of core genes.
A: Molecular docking revealed the binding of Dl-3-n-butylphthalide to its targets. Blue solid line: Hydrogen bond; Gray dashed line: Hydrophobic interaction; Yellow dashed line: Electrostatic interaction; B: The quantitative real-time polymerase chain reaction analysis of the mRNA levels of heme oxygenase 1, caspase 3, B cell leukemia/lymphoma 2, brain derived neurotrophic factor and nuclear factor erythroid 2 L2. Data expressed as individual values with mean ± SD. bP < 0.01, aP < 0.05. HMOX: Heme oxygenase; CASP3: Caspase 3; BCL2: B cell leukemia/lymphoma 2; BDNF: Brain derived neurotrophic factor; NFE2: Nuclear factor erythroid 2; HG: High glucose; NBP: Dl-3-n-butylphthalide.
- Citation: Wei WH, Bai YL, Zhu D, Zhang JY, Yin QC, Li Q, Shen CQ, Jin PS. Dl-3-n-butylphthalide ameliorates diabetic foot ulcer by inhibiting apoptosis and promoting angiogenesis. World J Diabetes 2025; 16(4): 101916
- URL: https://www.wjgnet.com/1948-9358/full/v16/i4/101916.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i4.101916