Objective: Residual scarring after cleft lip repair surgery remains a challenge for both surgeons and patients and novel therapeutics are critically needed. The objective of this preclinical experimental study was to evaluate the impact of the methyl-ester of pro-resolving lipid mediator lipoxin A (LXA-ME) on scarring in a novel rabbit model of cleft lip repair.

Methods: A defect of the lip was surgically created and repaired in eight six-week old New Zealand white rabbits to simulate human cleft lip scars. Rabbits were randomly assigned to topical application of PBS (control) or 1 ug of LXA-ME (treatment). 42 days post surgery all animals were euthanized. Photographs of the cleft lip area defect and histologic specimens were evaluated. Multiple scar assessment scales were used to compare scarring.

Results: Animals treated with LXA-ME exhibited lower Visual Scar Assessment scores compared to animals treated with PBS. Treatment with LXA-ME resulted in a significant reduction of inflammatory cell infiltrate and density of collagen fibers. Control animals showed reduced 2D directional variance (orientation) of collagen fibers compared to animals treated with LXA-ME demonstrating thicker and more parallel collagen fibers, consistent with scar tissue.

Conclusions: These data suggest that LXA-ME limits scarring after cleft lip repair and improves wound healing outcomes in rabbits favoring the resolution of inflammation. Further studies are needed to explore the mechanisms that underlie the positive therapeutic impact of LXA-ME on scarring to set the stage for future human clinical trials of LXA-ME for scar prevention or treatment after cleft lip repair.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094441PMC
http://dx.doi.org/10.3389/fimmu.2022.871200DOI Listing

Publication Analysis

Top Keywords

cleft lip
28
lip repair
16
scarring cleft
12
animals treated
12
collagen fibers
12
lip
8
lxa-me
8
lxa-me scarring
8
scar assessment
8
treated lxa-me
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!