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Pesticide residues in food — 2007: Toxicological ... - ipcs inchem

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67<br />

End-po<strong>in</strong>t Test object Concentration or dose Purity (%) Results References<br />

Chromosomal<br />

aberration<br />

Chromosomal<br />

aberration<br />

DNA damage<br />

Mouse bone marrow<br />

Mouse bone marrow<br />

Rat stomach, liver and<br />

kidney<br />

Males: 900–1750 mg/kg<br />

bw;<br />

Females: 1400, 1750 mg/kg<br />

bw; oral, s<strong>in</strong>gle dose<br />

125, 250, 500 mg/kg bw;<br />

<strong>in</strong>traperitoneal,<br />

two <strong>in</strong>jections 24 h apart<br />

875 mg/kg bw; oral, s<strong>in</strong>gle<br />

dose<br />

350 mg/kg bw per day;<br />

oral, 5 or 15 days<br />

DNA damage Rat lung 875 mg/kg bw; oral, s<strong>in</strong>gle<br />

dose<br />

350 mg/kg bw per day;<br />

oral, 5 or 15 days<br />

DNA damage<br />

Germ cells<br />

Chromosomal<br />

aberration<br />

Chromosomal<br />

aberration<br />

Chromosomal<br />

aberrations<br />

Dom<strong>in</strong>ant lethal<br />

mutation<br />

Dom<strong>in</strong>ant lethal<br />

mutation<br />

Dom<strong>in</strong>ant lethal<br />

mutation<br />

Dom<strong>in</strong>ant lethal<br />

mutation<br />

Sperm head<br />

morphology<br />

Mouse blood<br />

leukocytes<br />

Mouse spermatogonia<br />

Mouse spermatogonia<br />

Mouse spermatocytes<br />

Mouse spermiogenesis<br />

Mouse spermiogenesis<br />

Mouse spermiogenesis<br />

Mouse spermiogenesis<br />

Mouse sperm<br />

125, 250, 500 mg/kg bw;<br />

<strong>in</strong>traperitoneal<br />

444, 1332 mg/kg bw<br />

per day; oral, on five<br />

consecutive days<br />

6 mg/kg bw,<br />

<strong>in</strong>traperitoneal, s<strong>in</strong>gle dose<br />

1 ppm (dr<strong>in</strong>k<strong>in</strong>g-water) for<br />

7 weeks<br />

444, 1332 mg/kg bw; oral,<br />

five doses over 10 days<br />

1500, 2000 mg/kg bw; oral,<br />

s<strong>in</strong>gle dose<br />

444, 1332 mg/kg bw; oral,<br />

s<strong>in</strong>gle dose<br />

6 mg/kg, <strong>in</strong>traperitoneal,<br />

s<strong>in</strong>gle dose<br />

500, 1000, 2000, 2400 mg/<br />

kg bw; oral, s<strong>in</strong>gle dose<br />

600 mg/kg bw per day;<br />

<strong>in</strong>traperitoneal, on five<br />

consecutive days<br />

98.7 Negative<br />

<strong>in</strong> males<br />

Positive <strong>in</strong><br />

females<br />

Gebel et al.<br />

(1997)<br />

97.7 Negative Kligerman et al.<br />

(2000b)<br />

NR Positive P<strong>in</strong>o et al.<br />

(1988)<br />

NR Negative P<strong>in</strong>o et al.<br />

(1988)<br />

97.7 Equivocal Tennant et al.<br />

(2001)<br />

NR Negative Hool (1981b)<br />

NR Negative Chollet et al.<br />

(1982)<br />

NR Negative Hool (1981c)<br />

NR Positive Adler (1980)<br />

98.9 Negative Hool (1981d)<br />

NR Negative Chollet et al.<br />

(1982)<br />

97.1 Negative Hertner (1993)<br />

97.2 Negative Osterloh et al.<br />

(1983)<br />

NR, not reported.<br />

respectively, and 0, 0.7, 3.5 and 35.0 mg/kg bw per day for F 1<br />

males and 0, 0.8, 3.8 and 37.5 mg/kg<br />

bw per day for F 1<br />

females, respectively.<br />

No treatment-related mortality or signs of toxicity were observed dur<strong>in</strong>g the study. Parental<br />

body weights, body-weight ga<strong>in</strong>, and <strong>food</strong> consumption were statistically significantly reduced at<br />

500 ppm (the highest dose tested) <strong>in</strong> both sexes and both generations throughout the study. Compared<br />

with controls, body weights for F 0<br />

males and females at the highest dose at 70 days <strong>in</strong>to the study<br />

were decreased by 12% and 15%, respectively, while body weight of the F 1<br />

generation for the same<br />

period was decreased by 15% and 13% for males and females, respectively.<br />

ATRAZINE 37–138 JMPR <strong>2007</strong>

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