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Secoiridoids from the Seed of Gonocaryum calleryanum and Their Inhibitory Potential on LPS-Induced Tumor Necrosis Factor and Nitric Oxide Production.
Cheng, Kun-Ching; Chang, Chi-I; Lin, Yu-Chi; Liu, Chih-I; Zeng, Yu-Ci; Lin, Yun-Sheng.
Afiliação
  • Cheng KC; Taiwan Sugar Research Institute, Tainan 70176, Taiwan. a64128@taisugar.com.tw.
  • Chang CI; Department of Biological Science and Technology, National Pingtung University of Science and Technology, Pingtung 91201, Taiwan. changchii@mail.npust.edu.tw.
  • Lin YC; National Research Institute of Chinese Medicine, Taipei 11221, Taiwan. m8952612@hotmail.com.
  • Liu CI; Department of Nursing, Meiho University, Pingtung 91202, Taiwan. x00003077@meiho.edu.tw.
  • Zeng YC; Department of Biological Science and Technology, Meiho University, Pingtung 91201, Taiwan. x00011052@meiho.edu.tw.
  • Lin YS; Department of Biological Science and Technology, Meiho University, Pingtung 91201, Taiwan. x00010106@meiho.edu.tw.
Molecules ; 23(7)2018 07 04.
Article em En | MEDLINE | ID: mdl-29973552
ABSTRACT
Three new secoiridoid constituents, goncarin A−C (1⁻3), and a new derivative, goncarin A monoacetate (4), along with two known lignins, pinoresinol (5) and paulownin (6), were isolated from the seed of Gonocaryum calleryanum (Baill.) Becc. The structures of the new metabolites were determined on the basis of extensive spectroscopic analysis, particularly mass spectroscopy and 2D NMR (¹H⁻¹H COSY, HMQC, HMBC, and NOESY) spectroscopy. The aim of this study was to identify the anti-inflammatory effects of compounds 1⁻6 on lipopolysaccharide (LPS)-stimulated murine macrophage cell lines (RAW 264.7). Following stimulation with LPS, elevated levels of nitric oxide (NO) production were detected in RAW 264.7 cells; however, pretreatment with compounds 1⁻6 significantly inhibited the production of NO (around 40⁻80%, p < 0.01⁻0.05), by suppressing the expression of inducible NO synthase (iNOS). In addition, LPS-stimulated tumor necrosis factor-α (TNF-α) production was significantly reduced by compounds 1⁻3 (25⁻40%, p < 0.01⁻0.05). These results suggested that compounds 1⁻3 may exert anti-inflammatory activity, and that compounds 1⁻3 may be considered a potential therapeutic for the treatment of inflammatory diseases associated with macrophage activation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article