Accelerative action of topical piperonylic acid on mice full thickness wound by modulating inflammation and collagen deposition.
Karina Gomes MoreiraThais Paulino do PradoNatália Ferreira MendesRenan de Medeiros BezerraCarlos Poblete JaraMaria Helena Melo LimaEliana Pereira de AraújoPublished in: PloS one (2021)
Epidermal growth factor (EGF) promotes cell growth, proliferation, and survival in numerous tissues. Piperonylic acid, a metabolite present in peppers (Piper nigrum L. and Piper longum L.), can bind to the epidermal growth factor receptor (EGFR) and induce an intracellular signaling cascade leading to the transcription of genes responsible for these actions, especially in keratinocytes. These cells are fundamental in maintaining cutaneous homeostasis and are the first to be damaged in the case of a wound. Thus, we hypothesized that piperonylic acid improves wound healing. C57BL6/J male mice were submitted to dorsal skin wounds caused by a 6 mm punch and treated topically with piperonylic acid or vehicle. The wounds were evaluated macro- and microscopically, and tissue samples were collected for immunofluorescence and real-time PCR analyses on days 6, 9 and 19 post-injury. Topical piperonylic acid improved wound healing from day 6 post-injury until closure. This phenomenon apparently occurred through EGFR activation. In addition, piperonylic acid modulated the gene expression of interleukin (Il)-6, il-1β, tumor necrosis factor (Tnf)-α, il-10, monocyte chemoattractant protein (Mcp)-1 and insulin-like growth factor (Igf)-1, which are important for the healing process. By day 19 post-injury, the new tissue showed greater deposition of type I collagen and a morphology closer to intact skin, with more dermal papillae and hair follicles. We conclude that piperonylic acid may be a viable option for the treatment of skin wounds.
Keyphrases
- wound healing
- epidermal growth factor receptor
- gene expression
- growth factor
- small cell lung cancer
- tyrosine kinase
- signaling pathway
- dna methylation
- rheumatoid arthritis
- induced apoptosis
- spinal cord
- metabolic syndrome
- type diabetes
- immune response
- cell proliferation
- skeletal muscle
- transcription factor
- adipose tissue
- advanced non small cell lung cancer
- real time pcr
- endoplasmic reticulum stress
- surgical site infection
- cell death
- spinal cord injury
- neuropathic pain
- combination therapy
- tissue engineering