Single Dose of N-Acetylcysteine in Local Anesthesia Increases Expression of HIF1α, MAPK1, TGFβ1 and Growth Factors in Rat Wound Healing.
Wiktor PaskalMichał KopkaAlbert StachuraAdriana M PaskalPiotr PietruskiKacper PełkaAlan E WoessnerKyle P QuinnRyszard GalusJarosław WejmanPaweł K WłodarskiPublished in: International journal of molecular sciences (2021)
In this study, we aimed to investigate the influence of N-acetylcysteine (NAC) on the gene expression profile, neoangiogenesis, neutrophils and macrophages in a rat model of incisional wounds. Before creating wounds on the backs of 24 Sprague-Dawley rats, intradermal injections were made. Lidocaine-epinephrin solutions were supplemented with 0.015%, 0.03% or 0.045% solutions of NAC, or nothing (control group). Scars were harvested on the 3rd, 7th, 14th and 60th day post-surgery. We performed immunohistochemical staining in order to visualize macrophages (anti-CD68), neutrophils (anti-MPO) and newly formed blood vessels (anti-CD31). Additionally, RT-qPCR was used to measure the relative expression of 88 genes involved in the wound healing process. On the 14th day, the number of cells stained with anti-CD68 and anti-CD31 antibodies was significantly larger in the tissues treated with 0.03% NAC compared with the control. Among the selected genes, 52 were upregulated and six were downregulated at different time points. Interestingly, NAC exerted a significant effect on the expression of 45 genes 60 days after its administration. In summation, a 0.03% NAC addition to the pre-incisional anesthetic solution improves neovasculature and increases the macrophages' concentration at the wound site on the 14th day, as well as altering the expression of numerous genes that are responsible for the regenerative processes.
Keyphrases
- transcription factor
- poor prognosis
- wound healing
- genome wide analysis
- genome wide
- genome wide identification
- stem cells
- induced apoptosis
- surgical site infection
- oxidative stress
- nk cells
- signaling pathway
- cell proliferation
- mesenchymal stem cells
- cell death
- atrial fibrillation
- dna methylation
- transforming growth factor
- cell cycle arrest
- bone marrow