Literature DB >> 12598557

Neurotoxicity of dental amalgam is mediated by zinc.

D Lobner1, M Asrari.   

Abstract

The use of dental amalgam is controversial largely because it contains mercury. We tested whether amalgam caused toxicity in neuronal cultures and whether that toxicity was caused by mercury. In this study, we used cortical cell cultures to show for the first time that amalgam causes nerve cell toxicity in culture. However, the toxicity was not blocked by the mercury chelator, 2,3-dimercaptopropane-1-sulphonate (DMPS), but was blocked by the metal chelator, calcium disodium ethylenediaminetetraacetate (CaEDTA). DMPS was an effective mercury chelator in this system, since it blocked mercury toxicity. Of the components that comprise amalgam (mercury, zinc, tin, copper, and silver), only zinc neurotoxicity was blocked by CaEDTA. These results indicate that amalgam is toxic to nerve cells in culture by releasing zinc. While zinc is known to be neurotoxic, ingestion of zinc is not a major concern because zinc levels in the body are tightly regulated.

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Year:  2003        PMID: 12598557     DOI: 10.1177/154405910308200318

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  3 in total

1.  Cytotoxic evaluation of two orthodontic silver solder materials on human periodontal ligament fibroblast cells and the effects of antioxidant and antiapoptotic reagents.

Authors:  Ghada Nimeri; Joseph Curry; David Berzins; Dawei Liu; Bhoomika Ahuja; Douglas Lobner
Journal:  Angle Orthod       Date:  2021-05-01       Impact factor: 2.079

2.  Cytotoxicity of intermaxillary orthodontic elastics of different colors: an in vitro study.

Authors:  Rogério Lacerda Dos Santos; Matheus Melo Pithon; Gabriella Da Silva Mendes; Maria Teresa Villela Romanos; Antônio Carlos De Oliveira Ruellas
Journal:  J Appl Oral Sci       Date:  2009 Jul-Aug       Impact factor: 2.698

3.  The protective role of selenium against dental amalgam-induced intracellular oxidative toxicity through the TRPV1 channel in DBTRG glioblastoma cells.

Authors:  Derya Ceyhan; Kadriye Gorkem Ulu Guzel; Bilal Cig
Journal:  J Appl Oral Sci       Date:  2021-02-10       Impact factor: 2.698

  3 in total

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