Literature DB >> 14500036

Effect of three triterpenoid compounds isolated from root bark of Aralia elata on stimulus-induced superoxide generation and tyrosyl phosphorylation and translocation of p47(phox) and p67(phox) to cell membrane in human neutrophil.

Zhigang Wang1, Shaojiang Song, Huangwei Lu, Guang Chen, Suixu Xu, Yasuhiro Sagara, Noriko Kitaoka, Masanobu Manabe, Hiroyuki Kodama.   

Abstract

BACKGROUND: Root bark of Aralia elata is used as a folk medicine for neurasthenia, rheumatism, diabetes, hepatitis virus and spasm of the stomach in China, Japan and Russia.
METHODS: The effect of three triterpenoid compounds isolated from root bark of A. elata on stimulus-induced superoxide generation and tyrosyl phosphorylation and translocation of p47(phox) and p67(phox) to cell membrane was investigated. The three compounds examined were Elatoside A, Elatoside C, and Tarasaponin V.
RESULTS: When the cells were preincubated with these compounds, the superoxide generation induced by N-formyl-methionyl-leucyl-phenylalanine (fMLP) was suppressed in a low concentration range. However, the superoxide generation was significantly enhanced by 40 micromol/l triterpenoid, and was again suppressed in the higher concentration range. In the case of superoxide generation induced by phorbol 12-myristate 13-acetate (PMA), the compounds had no obvious effect on the superoxide generation in low concentration but suppressed that at 40 micromol/l. These compounds also efficiently suppressed the superoxide generation induced by arachidonic acid (AA) at 10 micromol/l. In parallel to the effect on the fMLP-induced superoxide generation, these compounds suppressed fMLP-induced tyrosyl phosphorylation and the translocation to membrane of cytosolic compounds, p47(phox) and p67(phox) at 10 and 80 micromol/l but not at 40 micromol/l.
CONCLUSIONS: Triterpenoid saponins examined in this study effect stimulus-induced superoxide generation and tyrosyl phosphorylation and translocation to membrane of p47(phox) and p67(phox) in a concentration-dependent manner, and may have some pharmaceutical applications.

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Year:  2003        PMID: 14500036     DOI: 10.1016/s0009-8981(03)00326-7

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  5 in total

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4.  Araloside C attenuates atherosclerosis by modulating macrophage polarization via Sirt1-mediated autophagy.

Authors:  Yun Luo; Shan Lu; Ye Gao; Ke Yang; Daoshun Wu; Xudong Xu; Guibo Sun; Xiaobo Sun
Journal:  Aging (Albany NY)       Date:  2020-01-27       Impact factor: 5.682

5.  Calenduloside E Analogues Protecting H9c2 Cardiomyocytes Against H2O2-Induced Apoptosis: Design, Synthesis and Biological Evaluation.

Authors:  Yu Tian; Yu-Yang Du; Hai Shang; Min Wang; Zhong-Hao Sun; Bao-Qi Wang; Di Deng; Shan Wang; Xu-Dong Xu; Gui-Bo Sun; Xiao-Bo Sun
Journal:  Front Pharmacol       Date:  2017-11-23       Impact factor: 5.810

  5 in total

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