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Multi-Omics Analysis of Anti-Inflammatory Action of Alkaline Extract of the Leaves of Sasa sp.
Sakagami, Hiroshi; Nakatani, Sachie; Enomoto, Ayame; Ota, Sana; Kaneko, Miku; Sugimoto, Masahiro; Horiuchi, Misaki; Toeda, Kazuki; Oizumi, Takaaki.
Afiliação
  • Sakagami H; Meikai University Research Institute of Odontology (M-RIO), Meikai University School of Dentistry, 1-1 Keyakidai, Sakado, Saitama 350-0283, Japan.
  • Nakatani S; Graduate School of Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado, Saitama 350-0295, Japan.
  • Enomoto A; Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0052, Japan.
  • Ota S; Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0052, Japan.
  • Kaneko M; Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0052, Japan.
  • Sugimoto M; Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0052, Japan.
  • Horiuchi M; Research and Development Center for Minimally Invasive Therapies, Institute of Medical Science, Tokyo Medical University, Shinjuku, Tokyo 160-0022, Japan.
  • Toeda K; Daiwa Biological Research Institute Co., Ltd., Sakado 3-2-1, Takatsu-ku, Kawasaki, Kanagawa 213-0012, Japan.
  • Oizumi T; Daiwa Biological Research Institute Co., Ltd., Sakado 3-2-1, Takatsu-ku, Kawasaki, Kanagawa 213-0012, Japan.
J Clin Med ; 10(10)2021 May 13.
Article em En | MEDLINE | ID: mdl-34068182
ABSTRACT
Efficient utilization of alkaline extracts of several plants for the treatment of oral diseases has been reported. To investigate the mechanism of anti-inflammatory activity of alkaline extract of the leaves of Sasa sp. (SE), multi-omics analysis using metabolomics and DNA array was performed. Human gingival fibroblasts (HGFs) were treated for IL-1ß to induce inflammation (detected by PGE2 production in culture medium) in the presence or absence of SE. Both IL-1ß and SE showed slight hormetic growth stimulation against HGF. SE inhibited PGE2 production dose- and time-dependently. Its inhibitory action was more pronounced by first treating the cells with SE, rather than with IL-1ß. At 3 h after IL-1ß treatment, 18 amino acids (except cysteine and glutamic acid), total glutathione (GSH, GSSG, Cys-GSH disulfide), Met-sulfoxide, 5-oxoproline, and SAM declined, whereas DNA expressions of AKT, CASP3, and CXCL3 were elevated. These changes were reversed by simultaneous treatment with SE. The present study suggests that the anti-inflammatory action of SE is mediated via various metabolic pathways for cell survival, apoptosis, and leukocyte recruitment.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article