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A combination of curcumin and ginger extract improves abrasion wound healing in corticosteroid‐impaired hairless rat skin
Author(s) -
Bhagavathula Narasimharao,
Warner Roscoe L.,
DaSilva Marissa,
McClintock Shan D.,
Barron Adam,
Aslam Muhammad N.,
Johnson Kent J.,
Varani James
Publication year - 2009
Publication title -
wound repair and regeneration
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.847
H-Index - 109
eISSN - 1524-475X
pISSN - 1067-1927
DOI - 10.1111/j.1524-475x.2009.00483.x
Subject(s) - hairless , curcumin , medicine , wound healing , skin repair , pharmacology , abrasion (mechanical) , skin irritation , dermatology , traditional medicine , surgery , chemistry , biochemistry , mechanical engineering , engineering
Hairless rats were topically treated with a combination of 10% curcumin and 3% ginger extract (or with each agent alone) for a 21‐day period. Following this, the rats were treated topically with Temovate (corticosteroid) for an additional 15 days. At the end of the treatment period, superficial abrasion wounds were induced in the treated skin. Abrasion wounds healed more slowly in the skin of Temovate‐treated rats than in skin of control animals. Healing was more rapid in skin of rats that had been pretreated with either curcumin or ginger extract alone or with the combination of curcumin–ginger extract (along with Temovate) than in the skin of rats treated with Temovate and vehicle alone. Skin samples were obtained at the time of wound closure. Collagen production was increased and matrix metalloproteinase‐9 production was decreased in the recently healed skin from rats treated with the botanical preparation relative to rats treated with Temovate plus vehicle. In none of the rats was there any indication of skin irritation during the treatment phase or during wounding and repair. Taken together, these data suggest that a combination of curcumin and ginger extract might provide a novel approach to improving structure and function in skin and, concomitantly, reducing formation of nonhealing wounds in “at‐risk” skin.