16:00 - 18:00
Room: San Francisco
Poster session
Inflammatory response of spilanthol on Human oral cells
Freitas Blanco Veronica Santana 1, 2, Rodrigues Rodney Alexandre Ferreira 2, Carvalho Joao Ernesto 3, Alonso Isabella Gonçalves 4, Pastre Julio Cezar 4, Murata Ramiro Mendonca 5
1 Pharmacology, Anesthesiology, and Therapeutics, Department of Physiological Sciences, Piracicaba Dental School, University of Campinas, Piracicaba, Brazil
2 Agricultural, Biological, and Chemical Research Center (CPQBA), Department of Chemistry of Natural Products, University of Campinas, Campinas, Brazil
3 Faculty of Pharmaceutical Sciences, University of Campinas, Campinas, Brazil
4 Chemistry Institute, University of Campinas, Campinas, Brazil
5 Department of Foundational Sciences, School of Dental Medicine, East Carolina University, Greenville, United States

Acmella oleracea (L.) R.K. Jansen, a herb native from Brazil, it is traditionally used in the culinary and to treat toothaches. Spilanthol is believed to be responsible for the anesthetic and anti-inflammatory effects presented by this species and therefore possess high therapeutic value [1]. Our study aimed to evaluate the cytotoxicity and the effect of spilanthol in human gingival fibroblast (HGF-1) focusing on the inflammatory pathway. Human gingival fibroblasts, HGF-1 (ATCC® CRL-2014) were seeded in 96 well plates and incubated with different concentrations of spilanthol (1-1000 µM) for 24, 48, and 72 h. Toxicity was evaluated using fluorometric quantification of cellular viability (Promega CellTiter-Blue). Cytokine production was analyzed by Human Inflammatory Cytokine Multi-Analyte ELISArray (Qiagen, MEH-004A) and gene expression profile was performed by RT2 Profiler PCR Array using The Human Inflammatory Response & Autoimmunity (Qiagen, PAHS-077Z). A decrease in cell viability was observed in cells exposed at the highest concentration tested (1000 µM) and in a time-dependent manner (Figure 1). Five out of 84 genes related to inflammatory and immune response were down-regulated when the cells were treated with 20 µM of spilanthol (fold change ≥2 and p-value < 0.05). The expression of some genes (e.g., SELE, CCL17, IL-9) were significantly down-regulated by spilanthol. However, Spilanthol (20 and 200 µM) did not affect the cytokine and chemokines levels in HGF-1 supernatant when compared to control. In conclusion, Spilanthol is a promising naturally occurring agent displaying low toxicity and anti-inflammatory activity. The putative pathway by which spilanthol affect inflammation process may involve the downregulation of cytokines and chemokine receptors.

Acknowledgements: Capes (grant # 006211/2015-01) and Fapesp (grant #2014/06461-2).

[1] Barbosa AF, de Carvalho MG, Smith RE, Sabaa-Srur AUO. Braz. J. Pharmacog. 2016;26(1):128-33.

Figure 1. The cytotoxic effects of spilanthol on human gingival fibroblast (HGF-1) cells.

Reference:
Mo-Poster Session 1-PO-51:
Session:
Poster Session 1
Presenter/s:
Veronica Santana Freitas Blanco
Presentation type:
Poster presentation
Room:
San Francisco
Date:
Monday, 4th September, 2017
Time:
16:00 - 18:00
Session times:
16:00 - 18:00