Targeting oxidative stress in diabetic wound repair: combined photobiomodulation and adipose-derived stem cell therapy
摘要
Type 2 diabetes mellitus (DM2) often goes undiagnosed, leads to long-term complications, and delays wound healing, posing a challenge in plastic surgery. This study studied the impacts of allogeneic adipose-derived stem cells (al-ADSCs) and photobiomodulation (PBM), individually and in combination, on wound healing in type 2 diabetic rats.
MethodsForty-eight rats with a delayed, ischemic, and infected wound model (DIIHWM), were infected with methicillin-resistant Staphylococcus aureus (MRSA) and assigned to four groups: untreated controls, wounds treated with al-ADSC, wounds exposed to PBM, and wounds receiving PBM combined with al-ADSC. Outcomes were assessed using stereological analyses including mast cells and qRT-PCR evaluation of oxidative stress–related genes, including NADPH oxidases (NOX1 and NOX4), catalase (CAT), and superoxide dismutase (SOD), during the inflammatory (day 4) and proliferative (day 8) phases in a DIIHWM.
ResultsBy days 4 and 8, all treated groups showed enhanced granulation tissue formation and reduced inflammatory activity compared with controls (p < 0.05). PBM and PBM+al-ADSC produced greater improvements than al-ADSC alone. On day 8, CAT gene expression increased in all treated groups, while SOD levels were significantly higher in PBM and PBM+al-ADSC groups relative to controls (p < 0.05). Conversely, NOX1 and NOX4 gene expressions were markedly reduced in PBM and PBM+al-ADSC groups compared with both controls and al-ADSC-treated animals (p < 0.05).
ConclusionsApplication of al-ADSC, PBM, or their combination promoted faster wound recovery in DIIHWM of diabetic animals by modulating inflammation, enhancing antioxidant defenses, and stimulating granulation tissue formation. The combined PBM+al-ADSC and PBM-alone strategies were more effective than al-ADSC alone, particularly in downregulating NOX1/NOX4 and upregulating SOD nd CAT.
Level of EvidenceNot gradable.