Pulmonary biochemical effects of inhaled phosgene in rats

J Toxicol Environ Health. 1986;19(3):413-23. doi: 10.1080/15287398609530939.

Abstract

Three exposure regimens were used to study the time course of indicators of lung damage and recovery response to single or repeated exposures to phosgene (COCl2). Rats were sacrificed immediately or throughout a 38-d recovery period after inhalation of 1 ppm COCl2 for 4 h, at intervals during a 7-h exposure to 1 ppm phosgene, or at several time points throughout a 17-d exposure to 0.125 and 0.25 ppm COCl2 (4 h/d, 5 d/wk) and during a 21-d recovery period. Regimen 1 revealed significantly elevated lung wet weight, lung nonprotein sulfhydryl (NPSH) content, and glucose-6-phosphate dehydrogenase (G6PD) activity that stayed elevated for up to 14 d. A significant decrease in body weight and food intake was observed 1 d after exposure. Regimen 2 caused a slight depression in NPSH content but did not affect G6PD activity. Regimen 3 animals showed sustained elevations in lung wet weight, NPSH content, and G6PD activity after 7 d of exposure. No significant changes in these endpoints were observed for the 0.125 ppm COCl2 group. No consistent elevation in hydroxyproline content was seen at either exposure concentration. Light microscopic examination of lung tissue exposed to 0.25 ppm COCl2 for 17 d revealed moderate multifocal accumulation of mononuclear cells in the centriacinar region. In summary, exposure to COCl2 caused changes similar in most ways to those observed for other lower-respiratory-tract irritants.

MeSH terms

  • Animals
  • Body Weight / drug effects
  • Glucosephosphate Dehydrogenase / analysis
  • Hydroxyproline / analysis
  • Lung / analysis
  • Lung / drug effects*
  • Lung / pathology
  • Male
  • Organ Size / drug effects
  • Phosgene / toxicity*
  • Rats
  • Rats, Inbred Strains
  • Sulfhydryl Compounds / analysis
  • Time Factors

Substances

  • Sulfhydryl Compounds
  • Phosgene
  • Glucosephosphate Dehydrogenase
  • Hydroxyproline