Abstract
Diabetes is a common disorder that is characterized by high blood glucose levels, polyuria, and polydipsia. As a result of chronically elevated blood glucose, impaired wound healing is one of the many serious issues that can occur in diabetic patients. Impaired wound healing and vascular disorders are the most prevalent of the diabetic complications and are caused by diminished angiogenesis, decreased lymphangiogenesis, and destruction of endothelial cells. Adenosine is a purine nucleoside, which is a key local stimulator of cell proliferation and wound healing. Adenosine could be activated by interaction with specific adenosine A1, A2A, A2B, and A3 receptors. In addition, occupancy of adenosine receptors (especially the A2A and A2B receptors with adenosine agonists) may accelerate wound healing and reduce proinflammatory cytokine secretion, including tumor necrosis factor-α and interleukin-6. Caffeine is a nonselective antagonist of all the adenosine receptor subtypes and has demonstrated physiological effects in
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