Hypoxia is a major stressor and a prominent feature of pathological conditions, such as
bacterial infections,
inflammation,
wounds, and cardiovascular defects. In this study, we investigated whether reoxygenation has a protective effect against
hypoxia-induced acute injury and
burn using the C57BL/6 mouse model. C57BL/6 mice were exposed to
hypoxia and treated with both acute and
burn injuries and were in
hypoxia until wound healing. Next, C57BL/6 mice were exposed to
hypoxia for three days and then transferred to normoxic conditions for reoxygenation until wound healing. Finally, skin
wound tissue was collected to analyze healing-related markers, such as
inflammation, vascularization, and
collagen.
Hypoxia significantly increased inflammatory cell infiltration and decreased vascular and
collagen production, and reoxygenation notably attenuated
hypoxia-induced infiltration of inflammatory cells, upregulation of pro-inflammatory
cytokine levels (IL-6 and TNF-α) in the
wound, and remission of
inflammation in the
wound. Immunofluorescence analysis showed that reoxygenation increased the expression of the
angiogenic factor α-SMA and decreased ROS expression in
burn tissues compared to
hypoxia-treated animals. Moreover, further analysis by qPCR showed that reoxygenation could alleviate the expression of hypoxic-induced inflammatory markers (IL-6 and TNF), increase angiogenesis (SMA) and
collagen synthesis (Col I), and thus promote wound healing. It is suggested that
oxygen can be further evaluated in combination with
oxygen-releasing materials as a supplementary
therapy for patients with chronic hypoxic
wounds.