A Free Fatty Acid Synthetic Agonist Accelerates Wound Healing and Improves Scar Quality in Mice

Author:

Prado Thais P.12,Jara Carlos P.12ORCID,Dias Bóbbo Vanessa C.12,Carraro Rodrigo S.23,Sidarta-Oliveira Davi23,de Mendonça Guilherme R. A.23,Velloso Licio A.23,Araújo Eliana P.12ORCID

Affiliation:

1. Nursing School, Laboratory of Cell Signaling Obesity and Comorbidities Center, OCRC, University of Campinas, Campinas, Brazil

2. Faculty of Medical Sciences, Laboratory of Cell Signaling, Obesity and Comorbidities Center – OCRC, University of Campinas, Campinas, Brazil

3. Faculty of Medical Sciences, University of Campinas, Campinas, Brazil

Abstract

Background Impaired wound healing is a health problem around the world, and the search for a novel product to repair wounded skin is a major topic in the field. GW9508 is a synthetic molecule described as a selective agonist of free fatty acid receptors (FFARs) 1 and 4, and there is evidence of its anti-inflammatory effects on several organs of the body. Purpose Here, we aimed to evaluate the effects of topical GW9508 on wound healing in mice. Research Design First, we used bioinformatic methods to determine the expression of FFAR1 and FFAR4 mRNA in the skin from a human cell atlas assembled with single-cell transcriptomes. Next, we employed 6-week-old C57BL6J mice with 2 wounds inflicted in the back. The mice were randomly divided into 2 groups, a control group, which received topical vehicle, and a treatment group, which received GW9508, for 12 days. The wound was monitored by photographic documentation every 2 days, and samples were collected at day 6 and 12 post injury for RT-PCR, western blot and histology analyses. Results: FFAR1 and FFAR4 mRNA are expressed in skin cells in similar amounts to those in other tissues. Topical GW9508 accelerated wound healing and decreased gene expression of IL-10 and metalloproteinase 9 on days 6 and 12 post injury. It increased the quantity of Collagen I and improved the organization of collagen fibres. Conclusions: Our results show that GW9508 could be an attractive drug treatment for wounded skin. Future studies need to be performed to assess the impact of GW9508 in chronic wound models.

Funder

Coordination for the Improvement of Higher Education Personnel – Brazil

Sao Paulo Research Foundation

Publisher

SAGE Publications

Subject

Research and Theory

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