Literature DB >> 23918232

Divergent immunomodulatory effects of extracts and phenolic compounds from the fern Osmunda japonica Thunb.

Xiao-xin Zhu1, Yu-jie Li, Lan Yang, Dong Zhang, Ying Chen, Eva Kmonickova, Xiao-gang Weng, Qing Yang, Zdeněk Zídek.   

Abstract

OBJECTIVE: To study possible immunobiological potential of Osmunda japonica Thunb.
METHODS: Immunomodulatory effects of ethanol extracts prepared from rhizomes of O. japonica and phenolic compounds isolated from the extracts were investigated under the in vitro conditions using the rat peritoneal cells (2×10(6)/mL; 24 h culture). Biosynthesis of nitric oxide (NO) was assayed by Griess reagent, production of prostaglandin E2 (PGE2) and secretion of cytokines were determined by enzyme-linked immunoabsorbent assay.
RESULTS: The extracts activated dose dependently, with the onset at 2.5-5 μmol/L concentrations, the high output NO production, and secretion of interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β). Mild enhancement of NO was produced by the aldehyde-type phenolics 4-hydroxybenzaldehyde and 3,4-hydroxybenzaldehyde. In contrasts, the acetone-type phenolics 4-hydroxybenzalacetone and 3,4-hydroxybenzalacetone inhibited production of immune mediators including cytokines (TNF-α, IL-1β, IL-6), NO, and PGE2. The 3,4-hydroxybenzalacetone was more effective than 4-hydroxybenzaldehyde. The IC50s estimates ranged within the interval of 5-10 μmol/L. No signs of cytotoxicity were observed up to the 50 μmol/L concentration of the compounds.
CONCLUSION: Phenolic compounds contained in medicinal herb Osmunda japonica possess distinct immunomodulatory activity.

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Year:  2013        PMID: 23918232     DOI: 10.1007/s11655-013-1460-4

Source DB:  PubMed          Journal:  Chin J Integr Med        ISSN: 1672-0415            Impact factor:   1.978


  32 in total

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Authors:  M A Marletta; P S Yoon; R Iyengar; C D Leaf; J S Wishnok
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7.  Inhibition of viral replication by interferon-gamma-induced nitric oxide synthase.

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8.  Evidence for antiviral effect of nitric oxide. Inhibition of herpes simplex virus type 1 replication.

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9.  Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production.

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