Literature DB >> 30792116

Wound healing activity of terpinolene and α-phellandrene by attenuating inflammation and oxidative stress in vitro.

Marcella Malavazi de Christo Scherer1, Franciane Martins Marques1, Mariana Moreira Figueira1, Maria Carolina Oliveira Peisino1, Elisângela Flávia Pimentel Schmitt1, Tamara P Kondratyuk2, Denise Coutinho Endringer1, Rodrigo Scherer1, Marcio Fronza3.   

Abstract

This study was undertaken to investigate the in vitro wound healing effects and the anti-inflammatory and antioxidant activities of terpinolene and α-phellandrene. The in vitro stimulatory effects on the proliferation and migration of fibroblasts were assessed using the scratch assay. The anti-inflammatory activity was evaluated using cell-based assays by investigating their influence on nitric oxide (NO), superoxide anion (O2•-), tumour necrosis factor-alpha (TNF-α) and interleukin 6 (IL-6) production and using the TNF-α-induced nuclear factor kappa (NF-κB) assay. Antioxidant activity was determined by the ABTS cation radical scavenging capacity, ferric reducing/antioxidant potential (FRAP), and NO free radical scavenging assays. Terpinolene and α-phellandrene significantly increased the migration and proliferation of fibroblasts and suppressed the pro-inflammatory cytokines IL-6 and TNF-α in a dose-dependent manner. Terpinolene and α-phellandrene at a concentration of 100 μM significantly inhibited NO production (41.3 and 63.8%, respectively) in a macrophage cell-culture-based assay, and resulted in reductions in O2•- production of 82.1 ± 3.5% and 70.6 ± 4.3%, respectively. Moreover, these monoterpenes were verified to suppress NF-κB activity. In summary, terpinolene and α-phellandrene may contribute to broadening clinical options in the treatment of wounds by attenuating inflammation and oxidative stress in vitro.
Copyright © 2019. Published by Elsevier Ltd.

Entities:  

Keywords:  Cytokines; Inflammation; Migration; Scratch assay; Wound healing

Mesh:

Substances:

Year:  2019        PMID: 30792116     DOI: 10.1016/j.jtv.2019.02.003

Source DB:  PubMed          Journal:  J Tissue Viability        ISSN: 0965-206X            Impact factor:   2.932


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