TY - JOUR
T1 - Topical Sulfamylon cream inhibits DNA and protein synthesis in the skin donor site wound
AU - Zhang, Xiao Jun
AU - Heggers, John P.
AU - Chinkes, David L.
AU - Wolf, Steven E.
AU - Hawkins, Hal K.
AU - Wolfe, Robert R.
N1 - Funding Information:
Supported by Shriners Hospital grants 8790 and 8490.
PY - 2006/5
Y1 - 2006/5
N2 - Background: Whereas Sulfamylon is effective in treatment of burn wound infection, controversy exists regarding its effect on the healing process. Methods: A partial thickness skin donor site wound was created on the back and indwelling catheters were placed in the carotid artery and jugular vein in rabbits under general anesthesia. Sulfamylon cream (8.5%, BERTEK Pharmaceuticals Inc., Morgantown, W Va) was applied on the wound, with either open or occlusive dressing. The control wound was covered with dressings only. On day 7 after injury, stable isotope tracers were infused to determine the fractional synthetic rate (FSR) of DNA, and FSR and fractional breakdown rate (FBR) of protein in the wound. Results: In the Sulfamylon-open dressing group, the DNA FSR was 1.3 ± 0.6%/day, the protein FSR was 8.0 ± 3.5%/day, and the net protein deposition (FSR - FBR) was -0.3 ± 3.7%/day. These values were lower (P < .01 to .05) than the corresponding values in the control group (DNA FSR: 2.9 ± 0.9%/day; protein FSR: 20.5 ± 8.4%/day; net protein deposition: 7.9 ± 6.0%/day). Sulfamylon cream selectively inhibited DNA FSR from the de novo base synthesis pathway (2.3 ± 1.2 vs 0.8 ± 0.5%/day, P < .05 vs control). With the occlusive dressing Sulfamylon cream did not decrease wound DNA FSR due to a stimulation of the base salvage pathway, but still decreased protein FSR (11.5 ± 5.1%/day, P < .05 vs control). Histologic slides indicated that Sulfamylon cream inhibited re-epithelialization, collagen formation, and angiogenesis in the wound. Conclusions: Topical Sulfamylon cream application inhibited DNA and protein synthesis in the wound, which would be expected to retard the healing process.
AB - Background: Whereas Sulfamylon is effective in treatment of burn wound infection, controversy exists regarding its effect on the healing process. Methods: A partial thickness skin donor site wound was created on the back and indwelling catheters were placed in the carotid artery and jugular vein in rabbits under general anesthesia. Sulfamylon cream (8.5%, BERTEK Pharmaceuticals Inc., Morgantown, W Va) was applied on the wound, with either open or occlusive dressing. The control wound was covered with dressings only. On day 7 after injury, stable isotope tracers were infused to determine the fractional synthetic rate (FSR) of DNA, and FSR and fractional breakdown rate (FBR) of protein in the wound. Results: In the Sulfamylon-open dressing group, the DNA FSR was 1.3 ± 0.6%/day, the protein FSR was 8.0 ± 3.5%/day, and the net protein deposition (FSR - FBR) was -0.3 ± 3.7%/day. These values were lower (P < .01 to .05) than the corresponding values in the control group (DNA FSR: 2.9 ± 0.9%/day; protein FSR: 20.5 ± 8.4%/day; net protein deposition: 7.9 ± 6.0%/day). Sulfamylon cream selectively inhibited DNA FSR from the de novo base synthesis pathway (2.3 ± 1.2 vs 0.8 ± 0.5%/day, P < .05 vs control). With the occlusive dressing Sulfamylon cream did not decrease wound DNA FSR due to a stimulation of the base salvage pathway, but still decreased protein FSR (11.5 ± 5.1%/day, P < .05 vs control). Histologic slides indicated that Sulfamylon cream inhibited re-epithelialization, collagen formation, and angiogenesis in the wound. Conclusions: Topical Sulfamylon cream application inhibited DNA and protein synthesis in the wound, which would be expected to retard the healing process.
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U2 - 10.1016/j.surg.2005.10.013
DO - 10.1016/j.surg.2005.10.013
M3 - Article
C2 - 16701096
AN - SCOPUS:33646410696
SN - 0039-6060
VL - 139
SP - 633
EP - 639
JO - Surgery
JF - Surgery
IS - 5
ER -