Phenolic Compounds Isolated fromCalea unifloraLess. Promote Anti-Inflammatory and Antioxidant Effects in Mice Neutrophils (Ex Vivo) and in Mice Pleurisy Model (In Vivo)

Author:

da Rosa Julia Salvan1,Nascimento Marcus Vinicius Pereira Dos Santos1,Parisotto Eduardo Benedetti2,Lima Tamires Cardoso3,Santin José Roberto4ORCID,Biavatti Maique Weber3,Zamoner Ariane2,Dalmarco Eduardo Monguilhott1ORCID,Fröde Tânia Silvia1ORCID

Affiliation:

1. Graduate Course of Pharmacy, Center of Health Sciences, Federal University of Santa Catarina (UFSC), Florianópolis, SC, Brazil

2. Department of Biochemistry, Center of Biological Sciences, Federal University of Santa Catarina (UFSC), Florianópolis, SC, Brazil

3. Department of Pharmaceutical Sciences, Center of Health Sciences, Federal University of Santa Catarina (UFSC), Florianópolis, SC, Brazil

4. Núcleo de Investigações Químico-Farmacêuticas, University of Vale do Itajaí (UNIVALI), Itajaí, SC, Brazil

Abstract

The literature shows that phenolic compounds possess important antioxidant and anti-inflammatory activities; however, the mechanism underlying these effects is not elucidated yet. The genusCaleais used in folk medicine to treat rheumatism, respiratory diseases, and digestive problems. In this context, some phenolic compounds were isolated with high purity fromCalea unifloraLess. and identified as noreugenin (NRG) andα-hydroxy-butein (AH-BU). The aim of this study was to analyze the effect of these compounds on cell viability, the activity of myeloperoxidase (MPO), and apoptosis of mouse neutrophils usingex vivotests. Furthermore, the effect of these compounds on the cytokines, interleukin 1 beta (IL-1β), interleukin 17A (IL-17A), and interleukin 10 (IL-10), and oxidative stress was investigated by analyzing lipid peroxidation (the concentration of thiobarbituric acid reactive substances (TBARS)) and activities of antioxidant enzymes, superoxide dismutase (SOD), catalase (CAT), and glutathione S-transferase (GST), using a murine model of neutrophilic inflammation. The NRG and AH-BU reduce MPO activity and increase neutrophil apoptosis (p<0.05). These compounds reduced the generation of oxygen reactive species and IL-1βand IL-17A levels but increased IL-10 levels (p<0.05). This study demonstrated that NRG and AH-BU show a significant anti-inflammatory effect by inhibiting the MPO activity and increasing neutrophil apoptosis in primary cultures of mouse neutrophils. These effects were at least partially associated with blocking reactive species generation, inhibiting IL-1βand IL-17A, and increasing IL-10 levels.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Hindawi Limited

Subject

Cell Biology,Immunology

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