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

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281<br />

Table 10. Tissue distribution of radiolabel <strong>in</strong> groups of rats receiv<strong>in</strong>g [ 14 C]dimethomorph at a<br />

higher dose of 10 mg/kg bw<br />

Tissue<br />

Recovery (% of the total radioactive <strong>residues</strong> <strong>in</strong> the adm<strong>in</strong>istered dose)<br />

t max<br />

24 h 168 h<br />

Males Females Males Females Males Females<br />

GIT contents 74.40 72.33 22.16 21.76 0.01 0.01<br />

GIT 5.30 3.87 2.19 3.35 0.00 0.00<br />

Carcass 4.61 3.62 0.96 3.86 0.04 0.04<br />

Liver 1.14 0.82 0.85 1.05 0.08 0.04<br />

Kidneys 0.08 0.07 0.04 0.08 0.00 0.00<br />

Erythrocytes 0.06 0.02 0.03 0.03 0.01 0.00<br />

Plasma 0.05 0.03 0.04 0.04 0.00 0.00<br />

Lungs 0.03 0.03 0.01 0.03 0.00 0.00<br />

Fat 0.02 0.06 0.00 0.04 0.00 0.00<br />

Heart 0.02 0.02 0.01 0.02 0.00 0.00<br />

Pancreas 0.02 0.02 0.01 0.03 0.00 0.00<br />

Testes 0.02 — 0.01 — 0.00 —<br />

Bone 0.01 0.00 0.00 0.01 0.00 0.00<br />

Muscle 0.01 0.00 0.00 0.02 0.00 0.00<br />

Spleen 0.01 0.01 0.00 0.01 0.00 0.00<br />

Thymus 0.01 0.01 0.00 0.01 0.00 0.00<br />

Adrenals 0.00 0.00 0.00 0.00 0.00 0.00<br />

Bone marrow 0.00 0.00 0.00 0.00 0.00 0.00<br />

Bra<strong>in</strong> 0.00 0.01 0.00 0.01 0.00 0.00<br />

Pituitary 0.00 0.00 0.00 0.00 0.00 0.00<br />

Thyroid 0.00 0.00 0.00 0.00 0.00 0.00<br />

Ovaries — 0.00 — 0.00 — 0.00<br />

Uterus — 0.02 — 0.01 — 0.00<br />

Total 85.79 80.98 26.29 30.37 0.14 0.10<br />

From Bounds (1995)<br />

GIT, gastro<strong>in</strong>test<strong>in</strong>al tract.<br />

dead had congested lungs and pallor of the liver, kidneys and spleen. Signs of toxicity were observed<br />

30 m<strong>in</strong> after dos<strong>in</strong>g, <strong>in</strong>clud<strong>in</strong>g hunched posture, pilo-erection, abnormal gait, lethargy, decreased<br />

respiratory rates. Recovery was not observed before 10 days after dos<strong>in</strong>g. Surviv<strong>in</strong>g animals showed<br />

no treatment-related pathological f<strong>in</strong>d<strong>in</strong>gs (Kynoch, 1985).<br />

To <strong>in</strong>vestigate the possible differences <strong>in</strong> isomer-specific toxicity <strong>in</strong> Wistar rats, groups of five<br />

male and five female overnight fasted rats were given the dimethomorph Z-isomer (purity not stated)<br />

as a s<strong>in</strong>gle doses at 0 or 5000 mg/kg bw <strong>in</strong> 0.1% Tween 80 by oral gavage. Rats were observed for 15<br />

days. The study complied with GLP.<br />

The only f<strong>in</strong>d<strong>in</strong>g <strong>in</strong> the treated rats was pale faeces <strong>in</strong> the first 2 days after dos<strong>in</strong>g. No signs of<br />

toxicity and no mortalities were recorded with<strong>in</strong> the 2 weeks of observation. Therefore, the median<br />

lethal dose (LD 50<br />

) was greater than 5000 mg/kg bw for males and female (Heusener & Jacobs,<br />

1987a).<br />

DIMETHOMORPH 273–315 JMPR <strong>2007</strong>

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