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(VCCEP) Tier 1 Pilot Submission for BENZENE - Tera

(VCCEP) Tier 1 Pilot Submission for BENZENE - Tera

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decreases in maternal weight gain, fetal body weight, and percentage of weight-retarded<br />

fetuses, as well as increased incidence of extra ribs and fused sternebrae. In a follow-up study<br />

(Tátrai et., 1980), concentrations of 0, 47, 140, 465, and 930 ppm (0, 150, 450 1500, and<br />

3000 mg/m 3 ) benzene were administered, 24hours/day, on GDs 7–14. Decreased maternal<br />

body-weight gains (not corrected <strong>for</strong> gravid uterus) were concentration dependent at doses of<br />

47–465 ppm, but decreases were less at 930 ppm. Fetal body weights were decreased at all<br />

doses, and fetal loss (30%–40% total implantation sites), and skeletal variations were increased<br />

at 140 ppm and above.<br />

When rats were exposed to benzene (400 mg/m 3 ) combined with toluene (100 mg/m 3 ) or xylene<br />

(600 mg/m 3 ), 24 hours/day on GDs 7–15, sacrificed on GD 21, decreased maternal weight gain<br />

and retardation of fetal and skeletal growth were observed, but no increases in skeletal<br />

anomalies, mal<strong>for</strong>mations or abnormal survivors occurred. Developmental effects of combined<br />

solvents were not additive. However, each solvent, when administered along with<br />

acetylsalicytic acid (ASA), enhanced expression of ASA-induced mal<strong>for</strong>mations (Ungváry and<br />

Tátrai, 1985).<br />

Benzene <strong>VCCEP</strong> <strong>Submission</strong><br />

March 2006<br />

74

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