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Transforming growth factor β plays an important role in enhancing wound healing by topical application of Povidone-iodine
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AbstractPovidone-iodine (PVI) is principally used as an antimicrobial agent. It has been found that 0.5% PVI can attenuate congestion, edema and pain induced by pressure sores. Thus this study aimed to assess the effects of 0.5% PVI on acute skin wounds. Four full-thickness excisional wounds were generated on the dorsal skin of male Sprague-Dawley rats with a 10-mm sterile punch. Two wounds were left untreated and the other two were dressed with gauze with 0.5% PVI for 1 hour per day for the first 5 days after injury. 10-mm full-thickness excisional wounds were also generated on the dorsal skin of rats treated with 10 mg/kg SB431542 and all wounds were treated with 0.5% PVI for 5 days. PVI treatment enhanced wound healing via promotion of expression of α SMA and TGF β, neovascularization and re-epithelialization. Interleukin 6 was reduced following PVI treatment. Inhibition of TGF β abolished the effect of PVI treatment on wound closure. These data show that topical application of 0.5% PVI could promote acute skin wound healing though increased expression of TGF β leading to enhanced formation of granulation tissue, even in the absence of obvious infection.
Springer Science and Business Media LLC
Title: Transforming growth factor β plays an important role in enhancing wound healing by topical application of Povidone-iodine
Description:
AbstractPovidone-iodine (PVI) is principally used as an antimicrobial agent.
It has been found that 0.
5% PVI can attenuate congestion, edema and pain induced by pressure sores.
Thus this study aimed to assess the effects of 0.
5% PVI on acute skin wounds.
Four full-thickness excisional wounds were generated on the dorsal skin of male Sprague-Dawley rats with a 10-mm sterile punch.
Two wounds were left untreated and the other two were dressed with gauze with 0.
5% PVI for 1 hour per day for the first 5 days after injury.
10-mm full-thickness excisional wounds were also generated on the dorsal skin of rats treated with 10 mg/kg SB431542 and all wounds were treated with 0.
5% PVI for 5 days.
PVI treatment enhanced wound healing via promotion of expression of α SMA and TGF β, neovascularization and re-epithelialization.
Interleukin 6 was reduced following PVI treatment.
Inhibition of TGF β abolished the effect of PVI treatment on wound closure.
These data show that topical application of 0.
5% PVI could promote acute skin wound healing though increased expression of TGF β leading to enhanced formation of granulation tissue, even in the absence of obvious infection.
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