Natural cocoa ingestion promotes wound healing in rats with diabetes by accelerated re-epithelialization and enhanced IGF-1 expression
Abstract
Background: Diabetic wounds (DWs) are difficult to manage due to delayed healing, increasing the risk of infection and limb amputation. Hyperglycemia impairs re-epithelialization and dermal cell proliferation, both key processes in wound closure. The persistent production of
advanced glycation end products (AGEs) further inhibits healing in diabetes. Cocoa is rich in polyphenols, offers antioxidants, antiinflammatory, and anti-glycemic properties that may support DW healing.
Aim: This study investigated the potential of natural cocoa powder in enhancing wound healing in experimentally streptozotocin (STZ)nicotinamide- induced type 2 diabetes mellitus (T2DM) rats.
Methods: T2DM was induced in rats using nicotinamide and STZ. Rats with diabetes were assigned to a cocoa-treated group (DC) and an untreated group (DU); rats without diabetes served as controls (C). Aqueous 2% natural cocoa was administered to the DC group for 6 weeks. Full-thickness dorsal wounds were created, and biopsies were taken on days 0, 3, 7, and 14. Wound contraction, epidermal thickness, and dermal cell counts were assessed histologically. IGF-1 expression was also evaluated via immunohistochemistry.
Conclusion: Cocoa-treated rats showed significantly enhanced wound contraction, thicker epidermis, and higher dermal cell counts. IGF-1 expression markedly increased in DC, compared to the control group.
