Comparison of the impact of continuous and intermittent exposure to vinyl chloride, including phenobarbital effect
Language English Country Czech Republic Media print
Document type Comparative Study, Journal Article
PubMed
4020114
Knihovny.cz E-resources
- MeSH
- Alanine Transaminase analysis MeSH
- Alkaline Phosphatase analysis MeSH
- Aspartate Aminotransferases analysis MeSH
- Time Factors MeSH
- Phenobarbital adverse effects MeSH
- Glutathione Transferase analysis MeSH
- Microsomes, Liver analysis enzymology MeSH
- Liver drug effects metabolism MeSH
- Rats MeSH
- L-Lactate Dehydrogenase analysis MeSH
- L-Iditol 2-Dehydrogenase analysis MeSH
- Body Weight drug effects MeSH
- Thioglycolates analysis urine MeSH
- Organ Size drug effects MeSH
- Vinyl Chloride adverse effects MeSH
- Vinyl Compounds adverse effects MeSH
- Environmental Exposure MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- Alanine Transaminase MeSH
- Alkaline Phosphatase MeSH
- Aspartate Aminotransferases MeSH
- Phenobarbital MeSH
- Glutathione Transferase MeSH
- L-Lactate Dehydrogenase MeSH
- L-Iditol 2-Dehydrogenase MeSH
- thiodiacetic acid MeSH Browser
- Thioglycolates MeSH
- Vinyl Chloride MeSH
- Vinyl Compounds MeSH
Rats were subjected to 4 h continuous and intermittent exposure to vinyl chloride (VC) at the time-weighted average concentration of 50,000 mg/m3. Prior to exposure, half of the animals obtained water, whereas the other half 0.1% sodium phenobarbital (PB) solution for seven consecutive days. The studies were focussed on: body weight, liver weight, activity of enzymes in the blood serum, activity of glutathione S-transferase in the liver cytoplasmatic and microsomal fraction, content of free non-protein sulfhydryl groups (NPSH) in the liver and urinary excretion of thiodiglycolic acid (TDGA). VC exposure, both continuous and intermittent, resulted in a decrease of body weight, NPSH depletion in the liver and TDGA urinary excretion. PB effects were manifested by the persistent decrease in rats' body weight, increase in the liver weight, increase in the cytoplasmatic activity of glutathione S-transferase in the liver and increase in TDGA urinary excretion. With none of the tested parameters, except TDGA, statistically significant differences between the continuous and intermittent VC exposure at the same time-weighted average concentration of 50,000 mg/m3, were found. TDGA urinary excretion was higher in rats poisoned in continuous exposure, as compared to the intermittent one.