The respiration of naive F344 rats confined in nose-only inhalation exposure tubes was measured to obtain data for normal adult rats of different ages and to evaluate the tubes for exposures lasting several hours. Exposure tubes were modified for use as volume-displacement plethysmographs. Respirati
1,2-Dichloropropane hepatotoxicity in rats after inhalation exposure
β Scribed by A. di Nucci; C. Gregotti; L. Manzo; M. Imbriani; S. Ghittori; L. Bianco; L. Maestri; E. Capodaglio
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 404 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0260-437X
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β¦ Synopsis
The hepatic effects of 1,2-dichloropropane (DCP) were investigated in male Wistar rats exposed to 15, 50, 100, 250, 450, 1000, 1300, 1800 or 4900 mg DCP At the end of a 4-h period of exposure, average blood DCP levels were 0.025 and 5.38 pg ml-' in animals treated with 15 and 1300 mg m-3, respectively. Blood DCP concentrations were correlated with the air DCP concentrations in the inhalation chamber. At DCP concentrations of 100 mg m-3 or higher, the liver non-protein thiol (NPT) content was significantly reduced. Assays performed 20 h after 4-h DCP exposure showed that exposure to 100-1000 mg DCP m-3 had no effect on hepatic. NPT levels. The NPT content increased only in the liver of rats exposed to higher (13004!300 mg m-') DCP concentrations. Treatment with DCP did not cause hepatic lipid peroxidation and did not modify total protein content. The observed changes in liver cell thiol homeostasis are likely to reflect the action of reactive intermediates formed during DCP metabolism. These changes can occur in rats following exposure to considerably low levels of DCP vapour.
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