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Dichlorvos (DDVP) Risk Characterization Document - California ...

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APPENDIX C<br />

NALED<br />

TOXICOLOGY OF NALED AND TRICHLORFON<br />

Naled, 1,2-dibromo-2,2-dichloroethyl dimethyl phosphate is an organophosphate with insecticidal<br />

activity. It is used on crops and in structures for insect control. In 1990, 450,000 pounds of naled<br />

applied in <strong>California</strong> and the distribution was 54% for lemons, 12% for oranges, 10% for fresh or<br />

processed grapes, 7% for safflower, and 3% for cotton (DPR, 1991).<br />

Acute toxicity<br />

Naled was acutely toxic to laboratory animals when administered by the oral, dermal, and inhalation<br />

routes. Cholinergic signs (such as salivation, convulsion, tremors, death) were observed in all the<br />

species tested. Pathological changes were observed in some tissues. Congested lungs and pale<br />

kidneys were observed in rats after oral exposure. The skin of rabbits exposed to naled dermally<br />

showed damage including necrosis, fibrosis, and ulceration. The lowest acute oral NOEL was 10<br />

mg/kg-day for cholinergic signs in rats and rabbits.<br />

Subchronic and chronic toxicity<br />

The current Toxicology Summary (8/25/94) shows that there are no data gaps. All of the following<br />

studies were conducted by gavage administration. No adverse effects were found in the mouse<br />

oncogenicity, rat teratology, rabbit teratology, or neurotoxicity studies. Adverse effects were found in<br />

the dog chronic, rat chronic and oncogenicity, and rat reproductive toxicity studies. In the dog chronic<br />

study, the adverse effects (NOEL = 0.2 mg/kg-day) were the inhibition of brain, plasma, and<br />

erythrocyte ChE activities, degeneration of the testes, focal mineralization of the spinal cord, and mild<br />

siderosis in the spleen. In the rat chronic and oncogenicity study, the NOEL was also 0.2 mg/kg-day<br />

for the inhibition of brain, plasma, and erythrocyte ChE activities. There was a slight increase in the<br />

incidence of mammary adenocarcinoma in male rats (by gavage). In the two-generation reproductive<br />

toxicity study with naled, the only significant parental effect was a dose-related decrease in body<br />

weight in all treated F 1 males during both pre- and post-mating periods. The effects on the pups<br />

included decreased survival, body weight, and number of pups at birth with a NOEL of 2 mg/kg-day.<br />

The only inhalation study reviewed showed corneal and nasal lesions in the rat exposed to naled (A<br />

3.4 ug/L) by inhalation for 3 weeks.<br />

Genotoxicity<br />

No adverse effects were found in the gene mutation (Ames assays), chromosomal aberration (bone<br />

marrow), and DNA damage (unscheduled DNA synthesis) studies.

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