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Influence of dental amalgam and heavy metal cations onin vitro interleukin-1? production by human peripheral blood mononuclear cells

✍ Scribed by Rausch-Fan, Xiaohui ;Schedle, Andreas ;Franz, Alexander ;Spittler, Andreas ;Gornikiewicz, Alexander ;Jensen-Jarolim, Erika ;Sperr, Wolfgang ;Boltz-Nitulescu, George


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
314 KB
Volume
51
Category
Article
ISSN
0021-9304

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✦ Synopsis


The influence of dental amalgam and heavy metal cations on interleukin-1␀ (IL-1␀) expression by peripheral blood mononuclear cells from healthy donors was studied. A marked decrease in the production of IL-1␀ was caused by freshly prepared amalgam or amalgamconditioned culture medium, but not by amalgam aged for 6 weeks. When metal cations were added as salts, Cu 2+ , Hg 2+ , and Ag + at high concentrations (33.3 and 333.3 M) were highly inhibitory. Among other heavy metal cations, Au 3+ , Pt 4+ , Ni 2+ , Pd 2+ , but not Ga 3+ or Sn 2+ , inhibited IL-1␀ production in a concentration-dependent manner. Flow cytometry studies indicated that Hg 2+ and Ag + strongly reduced the percentage of CD14 + cells containing IL-1␀ intracellularly. As shown by Northern blot analysis, Hg 2+ inhib-ited the level of IL-1␀-specific mRNA by 28% at 3.3 M and completely at 33.3 M. Only slight inhibitory effects were induced by Cu 2+ at 33.3 M. Interestingly, Ag + at a concentration of 3.3 M increased twofold the amount of IL-1␀specific mRNA. Our data show that IL-1␀ production is altered at protein and mRNA levels by components released from fresh amalgam and by other heavy metal cations, suggesting a role of these cations in changes in the cell phenotype and IL-1-mediated cell functions.


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The effects of dental amalgam on cytokine production by human peripheral blood mononuclear cells (PBMC) from healthy donors were analyzed. To induce cytokine production, PBMC were stimulated with lipopolysaccharide, phytohemagglutinin, or staphylococcal enterotoxin A and cultured for 48 h in the pre