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Volume 16, Issue 5, Pages 470-476 (May 2009)


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Bimodal effect of humic acids on the LPS-induced TNF-α release from differentiated U937 cells

R. Juneka, R. Morrowb, J.I. Schoenherra, R. Schuberta, R. Kallmeyera, S. Phullb, R. KlöckingaCorresponding Author Informationemail address

Abstract 

Humic substances (HS) have been reported to possess anti-inflammatory as well as pro-inflammatory properties. The anti-inflammatory activity was demonstrated in the rat paw edema model and we found a preliminary explanation in the 5-lipoxygenase inhibitory effect of humic acids (HA). The pro-inflammatory activity is reflected by the production and release of pro-inflammatory cytokines in HA-treated neutrophilic granulocytes. With regard to the potential use of HA as antiviral and UV-protective agents it appears advisable to investigate the role of HS in the inflammation process in more detail. Hence we tested four different HS preparations – two naturally occurring HA from the Altteich peatland in Germany, one fulvic acid (FA) preparation from a Finnish spruce forest and a synthetic HA-like polymer (caffeic acid oxidation product, KOP) for their influence on the lipopolysaccharide (LPS)-induced TNF-α release in human U937 cells. In addition, the cytotoxicity of HS was determined.

The results demonstrate a concentration-dependent bimodal effect of HA on the TNF-α release of differentiated LPS-stimulated U937 cells for both the natural black peat HA from the Altteich peatland and the HA-like polymer KOP. Low HA concentrations (10–80μg/ml) enhanced the TNF-α release by up to threefold (pro-inflammatory activity), while HA concentrations >100μg/ml reduced it about 10-fold (anti-inflammatory activity). FA failed to enhance TNF-α release, but reduced it at higher concentrations (>200μg/ml) by the half. Brown water HA did not exert any significant effect on TNF-α release. No HS-stimulated TNF-α release was also observed in the absence of exogenously supplied LPS. This means that HS, unlike endotoxin, are no inflammation-causing agents for LPS-untreated cells. Differences in the effect of individual HS on TNF-α release are discussed in connection with the polyanionic character of HS, their molecular mass distribution and the hitherto imperfectly known chemical structure.

a Department of Natural Sciences, Zittau/Görlitz University of Applied Sciences, D-02763 Zittau, Germany

b Department of Biological and Molecular Sciences, Faculty of Health and Life Sciences, Coventry University, CV 5FB Coventry, UK

Corresponding Author InformationCorresponding author. Tel.: +493583612303; fax: +493583612300.

PII: S0944-7113(08)00189-X

doi:10.1016/j.phymed.2008.10.003


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