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Evaluation of the wound healing process in rat skin using a hexanoyl group‐modified alkaline‐treated gelatin porous film
Author(s) -
Koga Takashi,
Kibe Toshiro,
Taguchi Tetsushi,
Fuchigami Takao,
Nishihara Kazuhide,
Ishihata Kiyohide,
Nakamura Norifumi
Publication year - 2021
Publication title -
oral science international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.256
H-Index - 13
eISSN - 1881-4204
pISSN - 1348-8643
DOI - 10.1002/osi2.1077
Subject(s) - wound healing , fibronectin , angiogenesis , gelatin , epithelium , chemistry , myofibroblast , anatomy , pathology , materials science , surgery , biomedical engineering , medicine , extracellular matrix , fibrosis , biochemistry
The present study investigated the wound healing process in a rat skin wound model dressed with a hexanoyl group‐modified alkaline‐treated gelatin porous (HxAlGltn) film with angiogenesis‐inducing and strong bioadhesive properties or a collagen sponge (CS). A circular 10‐mm full‐thickness skin defect was created on the backs of 8‐week‐old rats and then dressed with a HxAlGltn film (HxAlGltn group), collagen sponge (CS group), and no dressing (control group). Wound distances and areas were assessed macroscopically at specific time points after surgery, the lengths and thicknesses of the neo‐epithelium histologically, and α‐smooth muscle actin (α‐SMA), collagen type I, and fibronectin immunohistochemically. Wound distances and areas were significantly greater in the HxAlGltn group than in the CS and control groups. The expression of α‐SMA in myofibroblasts was significantly weaker in the HxAlGltn group than in the other groups on day 7. Furthermore, angiogenesis was prominent on days 4 and 7 in the HxAlGltn group. No significant differences were observed in the length of the neo‐epithelium between all groups, whereas the thickness of the neo‐epithelium was greater in the HxAlGltn group than in the CS group. The present results suggest the potential of the HxAlGltn film as a dressing material in the wound healing process of full‐thickness skin defects because it reduces scar contraction and promotes angiogenesis more than CS.