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Effect of Elaeagnus umbellata (Thunb.) fruit extract on H2O2-induced oxidative and inflammatory responses in normal fibroblast cells.
Zglinska, Klara; Niemiec, Tomasz; Lozicki, Andrzej; Matusiewicz, Magdalena; Szczepaniak, Jaroslaw; Puppel, Kamila; Kutwin, Marta; Jaworski, Slawomir; Rygalo-Galewska, Anna; Koczon, Piotr.
Afiliação
  • Zglinska K; Institute of Animal Science, Warsaw University of Life Sciences, Warsaw, Poland.
  • Niemiec T; Institute of Animal Science, Warsaw University of Life Sciences, Warsaw, Poland.
  • Lozicki A; Institute of Animal Science, Warsaw University of Life Sciences, Warsaw, Poland.
  • Matusiewicz M; Institute of Biology, Warsaw Univeristy of Life Sciences, Warsaw, Poland.
  • Szczepaniak J; Institute of Biology, Warsaw Univeristy of Life Sciences, Warsaw, Poland.
  • Puppel K; Institute of Animal Science, Warsaw University of Life Sciences, Warsaw, Poland.
  • Kutwin M; Institute of Biology, Warsaw Univeristy of Life Sciences, Warsaw, Poland.
  • Jaworski S; Institute of Biology, Warsaw Univeristy of Life Sciences, Warsaw, Poland.
  • Rygalo-Galewska A; Institute of Animal Science, Warsaw University of Life Sciences, Warsaw, Poland.
  • Koczon P; Institute of Food Science, Warsaw University of Life Sciences, Warsaw, Poland.
PeerJ ; 9: e10760, 2021.
Article em En | MEDLINE | ID: mdl-33552740
ABSTRACT

BACKGROUND:

Elaeagnus umbellata is a plant commonly used in traditional Asian medicine for its many health benefits and strong antioxidative activity. Its therapeutic potential is believed to be connected to its effect on fibroblasts. This study aimed to investigate E. umbellata methanol-acetone extract's (EUE) defense against hydrogen peroxide (H2O2)-induced fibroblast damage.

METHODS:

Because the main biologically active compounds of E. umbellata are water-insoluble, we evaluated the effects of methanol-acetone fruit extracts using liquid chromatography (for ascorbic acid and beta-carotene) and spectrophotometry (for lycopene and total phenolics). The extract's antioxidative activity was measured using DPPH radical inhibition, and EUE's effect on human fibroblasts was also evaluated. We assessed the metabolic activity and apoptosis of HFFF-2 fibroblasts exposed to EUE and/or H2O2using the XTT test and flow cytometry, respectively. Superoxide dismutase activity and reactive oxygen species (ROS) production were evaluated using colorimetric and fluorometric assays, respectively. We measured pro-inflammatory cytokine (MIF, fractalkine, MCP-4, BLC, GCP-2, NAP-2, Eotaxin-2, and Eotaxin-3) expression in HFFF-2 cells using immunocytochemistry.

RESULT:

The extract increased HFFF-2 cell proliferation and reduced cell death caused by H2O2-induced stress. H2O2-treated fibroblasts had greater ROS production than cells treated with both H2O2 and EUE. Additionally, the group treated with H2O2 alone showed higher pro-inflammatory cytokine (MIF, MCP-4, NAP-2, Eotaxin-2, and Eotaxin-3) expression.

CONCLUSION:

EUE protected human fibroblasts from H2O2-induced oxidative stress and reduced the fibroblast-mediated inflammatory response triggered by ROS.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: PeerJ Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Polônia

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: PeerJ Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Polônia