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Minerva Biotechnology and Biomolecular Research 2021 Apr 19

DOI: 10.23736/S2724-542X.21.02793-0


language: English

Hyperglycaemia-induced impaired neutrophil activity in the dynamic of burn wound healing in rats

Larysa V. NATRUS 1, Irina M. RYZHKO 1, Olha O. LISAKOVSKA 2

1 Department of modern technologies of medical diagnostics and treatment, Bogomolets National Medical University, Kyiv, Ukraine; 2 Department of Biochemistry of Vitamins and Coenzymes, Palladin Institute of Biochemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine


BACKGROUND: Understanding mechanisms underlying hyperglycaemia-induced dysfunctions in burn wound healing is an important biomedical issue. The aim is to assess how changes in systemic neutrophil functional activity in bone marrow (BM) and peripheral blood (PB) correlate with their recruitment to the burn wound site and the efficiency of wound healing in rats with altered glucose metabolism.
METHODS: Diabetes mellitus (DM) was developed in Wistar male rats (176,8±8,3 g) by streptozotocin injection (50 mg/kg b.w.). Skin burn injury was induced in control and DM groups (n=24) and healing dynamic was assessed (3, 7, 14, 21 days). The myeloperoxidase (MPO) activity in BM cells was assayed cytochemically. MPO content in regenerated tissue was determined by western blotting. Phagocytic index of PB neutrophils was assessed by latex test.
RESULTS: DM group showed less healing rate (contraction to 35.8% from initial wound size compared with 25% in control on day 21). Hyperglycaemia led to increased MPO activity in BM neutrophils (7 day - 18.97%, 14 - 20.15%, 21 - 14.34% vs. control). We detected hyperglycaemia-induced decrease in MPO content in tissue regenerate at the early stage (3 day - 66%, 7 - 44.4%) that reflects local neutrophil dysfunction. A tight correlation between wound contraction dynamics and phagocytic index of PB neutrophils was found.
CONCLUSIONS: Burn injury in DM group was accompanied by an altered pattern of neutrophilic activity and recruitment at early stages - reduced ability to phagocytose, declined MPO content in skin regenerate and elevated MPO activity in BM that resulted in the inhibition of the wound closure rate.

KEY WORDS: Burn wound healing; Neutrophils; Myeloperoxidase; Hyperglycaemia; Diabetes mellitus

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