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Vinyl Chloride - Texas Commission on Environmental Quality

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<str<strong>on</strong>g>Vinyl</str<strong>on</strong>g> chloride<br />

Page 12<br />

Wisniewska-Knypl et al. (1980) evaluated the toxicity of VC in male Wistar rats. Rats (7-10 per group)<br />

were exposed via inhalati<strong>on</strong> to 0, 50, 500, and 20,000 ppm VC for 5 h/day, 5 days/week for up to 10<br />

m<strong>on</strong>ths. Sacrifices were performed at 1, 3, 6, and 10 m<strong>on</strong>ths. This experiment was designed to examine<br />

the effects of VC <strong>on</strong> the activity of cytochrome P-450 m<strong>on</strong>ooxygenase and the ultrastructure of the liver.<br />

A statistically significant decrease in body weight was reported at 20,000 ppm after 10 m<strong>on</strong>ths. Relative<br />

liver weight was significantly increased at 500 and 20,000 ppm after all sacrifices. Electr<strong>on</strong> microscopic<br />

examinati<strong>on</strong> of the liver tissue from rats exposed to 50 ppm showed hepatocellular changes characterized<br />

by proliferati<strong>on</strong> of the smooth endoplasmic reticulum at 3 m<strong>on</strong>ths (although this effect subsided by 6<br />

m<strong>on</strong>ths) and accumulati<strong>on</strong> of lipid droplets in the cytoplasm after 10 m<strong>on</strong>ths. Rats exposed to 500 and<br />

20,000 ppm for 3 m<strong>on</strong>ths exhibited hypertrophy of the smooth endoplasmic reticulum, distensi<strong>on</strong> of<br />

canals of rough-surfaced membranes, swelling of mitoch<strong>on</strong>dria, and an increased number of lipid droplets<br />

in cytoplasm. These changes persisted through the 10 m<strong>on</strong>ths of the study and were more intensive at<br />

20,000 ppm. A LOAEL of 50 ppm was identified in this study for the 10 m<strong>on</strong>th exposure period based <strong>on</strong><br />

minor liver effects (accumulati<strong>on</strong> of lipid droplets).<br />

Torkels<strong>on</strong> et al. (1961) evaluated the toxicity of VC in rats, guinea pigs, rabbits, and dogs. Animals were<br />

exposed by inhalati<strong>on</strong> to 0, 50, 100, 200, or 500 ppm VC for 1.5 to 7 h/day for 4.5 to 6 m<strong>on</strong>ths. Growth,<br />

mortality, organ weight, and body weight were recorded for all animals. Hematology, histopathology, and<br />

urinalysis were also performed. Histopathological changes and increased liver weights were observed<br />

after repeated exposure to 500 ppm in rats. Repeated exposure to 200 ppm for 6 m<strong>on</strong>ths resulted in<br />

increased average liver weights of rats and micropathological changes in livers of rabbits. Repeated<br />

exposure to 100 ppm 7 h/day for 6 m<strong>on</strong>ths resulted in increased liver weight in rats. The NOAEL reported<br />

for this study is 50 ppm and the LOAEL is 100 ppm for increased relative liver weight in rats.

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