7). Through ROS-mediated reactions, metals cause “indirect” DNA damage, lipid peroxidation, and protein

modification. Metal-induced formation of free radicals has most significantly been evidenced for iron and copper then for chromium and partly for cobalt. The “direct” damage by metals may involve conformational changes to biomolecules due to the coordinated metal. Studies with cadmium revealed that the primary route for its toxicity is depletion of glutathione and bonding to sulphydryl groups of proteins. It has been described that arsenic also binds directly to critical thiols, however, an alternative mechanism leading to formation of hydrogen peroxide by oxidation of As(III) to As(V) under physiological conditions has been proposed. Nitric oxide seems to be involved in arsenite induced Pirfenidone in vitro DNA damage and pyrimidine excision

inhibition. Arsenic-induced formation of free radicals and Inhibitor Library concentration depletion of antioxidant pools results in disruption of the antioxidant/prooxidant equilibrium of cells. Metals interfere with cell signalling pathways and affect growth receptors, tyrosine and serine/threonine kinases, and nuclear transcription factors by ROS-dependent and ROS-independent mechanisms. Many of the DNA base modifications caused by free radicals are pro-mutagenic, pointing to a strong link between oxidative damage and the carcinogenesis of metals. Various antioxidants (both enzymatic and non-enzymatic) provide protection against deleterious metal-mediated free radical attacks. Generally, antioxidants can protect against redox-metal (iron, copper) toxicity by (i) chelating ferrous ion and preventing see more the reaction with molecular oxygen or peroxides, (ii) chelating iron and maintaining it in a redox state that makes iron unable to reduce molecular oxygen

and (iii) trapping any radicals formed. One of the most effective classes of antioxidants are thiol compounds, especially glutathione, which provide significant protection by trapping radicals, reduce peroxides and maintain the redox state of the cell. The non-enzymatic antioxidant vitamin E can prevent the majority of metal-mediated damage both in vitro systems and in metal-loaded animals. As outlined above, metal-induced oxidative stress is linked with a number of diseases and results partly from declined antioxidant mechanisms. Thus design of dual functioning antioxidants, possessing both metal-chelating and ROS/RNS-scavenging properties is awaited. None. The authors appreciate funding by the Scientific Grant Agency of the Slovak Republic (Projects VEGA #1/0856/11 and #1/0018/09) and by the Slovak Research and Development Agency of the Slovak Republic under the contract No. VVCE-0004-07. “
“Synthetic amorphous silica (SAS) consists of nano-sized primary particles, of nano- or micrometre-sized aggregates and of agglomerates in the micrometre-size range.