Stryphnodendron adstringens have a modulatory effect on inflammatory cytokines markers of in vitro activated macrophages

Author:

da Cruz Ivana Beatrice Mânica1ORCID,Teixeira Cibele Ferreira2ORCID,Pellenz Neida Luiza2ORCID,Mastella Moisés Henrique3ORCID,Azzolin Verônica Farina4ORCID,Ribeiro Euler Esteves5ORCID,Barbisan Fernanda1ORCID

Affiliation:

1. Postgraduate Program of Pharmacology, Federal University of Santa Maria, Santa Maria 97105-900, Brazil; Postgraduate Program of Gerontology, Federal University of Santa Maria, Santa Maria 97105-900, Brazil

2. Postgraduate Program of Pharmacology, Federal University of Santa Maria, Santa Maria 97105-900, Brazil

3. Department of Biophysics and Pharmacology, Institute of Biosciences of Botucatu, Universidade Estadual Paulista, Botucatu 18618-689, Brazil

4. Postgraduate Program of Gerontology, Federal University of Santa Maria, Santa Maria 97105-900, Brazil; Fundação Universidade Aberta da Terceira Idade, Manaus 69029-040, Brazil

5. Fundação Universidade Aberta da Terceira Idade, Manaus 69029-040, Brazil

Abstract

Aim: The purpose of this study is to conduct a comprehensive investigation into the modulatory effects of Stryphnodendron adstringens (Mart.; S. adstringens), a Brazilian wound-healing plant, on the expression of inflammatory cytokines. This will be achieved using an in vitro protocol with the commercial macrophage cell line RAW 264.7. Methods: The macrophage inflammatory response was induced by the natural antigen phytohemagglutinin (PHA), with and without supplementation of different concentrations of S. adstringens extract. The effects on cell proliferation rate and the concentration and production of transcripts of pro-inflammatory cytokines interleukin 1β (IL-1β), IL-6, tumor necrosis factor-alpha (TNF-α), and interferon-gamma (IFN-γ), as well as the anti-inflammatory cytokine IL-10, were assessed using spectrophotometric, immunoassay, and quantitative reverse transcription-polymerase chain reaction (qRT-PCR) techniques. Results: S. adstringens extract at all concentrations tested here reduced the cellular proliferation rate of activated macrophages. Extracts at concentrations of 0.49 mg/mL and 0.99 mg/mL decreased the protein and gene expression of pro-inflammatory cytokines, exhibiting the opposite effect concerning IL-10. Conclusions: The findings suggest that the wound-healing action of S. adstringens may encompass differential modulation of inflammation associated with tissue injury.

Publisher

Open Exploration Publishing

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