Literature DB >> 3388435

Comparative toxicity of nickel oxide, nickel sulfate hexahydrate, and nickel subsulfide after 12 days of inhalation exposure to F344/N rats and B6C3F1 mice.

J K Dunnick1, J M Benson, C H Hobbs, F F Hahn, Y S Cheng, A F Eidson.   

Abstract

The relative toxicity of nickel oxide (NiO), nickel sulfate hexahydrate. (NiSO4.6H2O), and nickel subsulfide (Ni3S2) was studied in F344/N rats and B6C3F1 mice after inhalation exposure for 6 h/day, 5 days/week for 12 exposure days. Exposure concentrations used (as mg Ni/m3) were 0.9-23.6 for NiO; 0.8-13.3 for NiSO4.6H2O, and 0.4-7.3 for Ni3S2. For each compound there were 5 exposure groups plus a control group. NiSO4.6H2O was the most toxic compound with exposure related mortality seen at exposure concentrations of 13.3 mg/m3 in rats and 1.6 mg/m3 and above in mice. For Ni3S2, mortality was seen in mice (but not in rats) at the highest exposure concentration (7.3 mg/m3). No mortality was seen after NiO exposure. Lesions of the lung and nasal cavity were seen in both rats and mice after exposure to NiSO4.6H2O and Ni3S2 at the 4 highest exposure concentrations. Lesions of the lung were seen primarily at the highest exposure concentrations after NiO exposure. The amount of nickel in the lungs at the end of exposure varied in relation to the water solubility of the compounds. Based on these 2-week studies, the toxicity ranking was NiSO4.6H2O greater than Ni3S2 much greater than NiO. Additional studies are in progress to assess the relative toxicities of these three nickel compounds after 90-day exposures.

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Year:  1988        PMID: 3388435     DOI: 10.1016/0300-483x(88)90087-x

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  6 in total

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2.  Effects of nickel oxide on the production of tumor necrosis factor by alveolar macrophages of rats.

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3.  Physical Characterization and Cellular Toxicity Studies of Commercial NiO Nanoparticles.

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4.  Pulmonary clearance and inflammatory potency of intratracheally instilled or acutely inhaled nickel sulfate in rats.

Authors:  S Hirano; T Shimada; J Osugi; N Kodama; K T Suzuki
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

Review 5.  Genetic and epigenetic mechanisms in metal carcinogenesis and cocarcinogenesis: nickel, arsenic, and chromium.

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Journal:  Chem Res Toxicol       Date:  2007-10-30       Impact factor: 3.739

Review 6.  Epidemiological and experimental aspects of metal carcinogenesis: physicochemical properties, kinetics, and the active species.

Authors:  L Magos
Journal:  Environ Health Perspect       Date:  1991-11       Impact factor: 9.031

  6 in total

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