Pulmonary toxicity caused by acute exposure to mercury vapor is enhanced in metallothionein-null mice

Life Sci. 1999;64(20):1861-7. doi: 10.1016/s0024-3205(99)00129-0.

Abstract

This study examined the protective role of metallothionein (MT) against pulmonary damage caused by acute exposure to metallic mercury (Hg0) vapor using MT-null and wild-type mice. Both strains of mice were exposed to Hg0 at 6.6 to 7.5 mg/m3 for 4 hr each day for 3 consecutive days. This dosing protocol was lethal to over 60% of MT-null mice but did not kill any wild-type mice. More severe pulmonary damage was found by histopathological observation in MT-null mice than in wild-type mice. MT levels in the lung were elevated in wild-type mice after Hg0 vapor exposure, and gel filtration of the lung cytosol revealed that most of the mercury was associated with MT. In MT-null mice, MT levels were below the limit of detection (0.2 microg/g tissue) for the MT assay even after exposure. After exposure to Hg0 vapor for 3 consecutive days, the pulmonary mercury levels in wild-type mice were significantly higher than in MT-null mice. These findings suggest that MT plays a protective role against the acute pulmonary toxicity of Hg0 vapor.

MeSH terms

  • Administration, Inhalation
  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Blood Urea Nitrogen
  • Chromatography, Gel
  • Creatinine / blood
  • Lung / drug effects*
  • Lung / metabolism
  • Lung / pathology
  • Lung Diseases / chemically induced*
  • Lung Diseases / metabolism
  • Lung Diseases / mortality
  • Lung Diseases / pathology
  • Mercury / metabolism
  • Mercury / toxicity*
  • Metallothionein / deficiency
  • Metallothionein / genetics
  • Metallothionein / metabolism
  • Metallothionein / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Radioimmunoassay
  • Survival Rate
  • Volatilization

Substances

  • Metallothionein
  • Creatinine
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Mercury