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toxicological profile for malathion - Agency for Toxic Substances and ...

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MALATHION 98<br />

3. HEALTH EFFECTS<br />

dermal toxicity of a <strong>malathion</strong> <strong>for</strong>mulation commonly used to treat house pets. A dog was sprayed over<br />

the entire body with a solution containing 0.5% <strong>malathion</strong> 3 times in a week <strong>and</strong> was observed <strong>for</strong> up to<br />

41 days following the treatment; plasma <strong>and</strong> RBC cholinesterase were also determined. No clinical signs<br />

of toxicity were observed during the study, but both plasma <strong>and</strong> RBC cholinesterase activities were<br />

inhibited by application of <strong>malathion</strong>. A maximum inhibition of 36% of the plasma cholinesterase<br />

activity <strong>and</strong> 34% of the RBC activity occurred the day of the second treatment, but by day 19, enzyme<br />

activities had recovered to pretreatment values. No doses could be estimated from these two studies.<br />

Repeated dermal doses of 200 mg/kg/day of <strong>malathion</strong> (98% pure) in acetone, which were lethal to<br />

guinea pigs, inhibited brain <strong>and</strong> RBC cholinesterase activity by 45–52% after 30 days of treatment, but<br />

did not induce gross or microscopical alterations in the brain (Dikshith et al. 1987). The animals that died<br />

showed frank signs of cholinergic stimulation be<strong>for</strong>e dying. A 65%, inhibition of cerebrum<br />

cholinesterase activity was reported in male New Zeal<strong>and</strong> rabbits applied <strong>malathion</strong> (94% pure) on the<br />

skin <strong>for</strong> 6 hours/day, 5 days/week <strong>for</strong> 3 weeks (Moreno 1989). Doses of 300 mg/kg/day decreased RBC<br />

cholinesterase activity by 26% in females, whereas the lowest dose level tested, 50 mg/kg/day, caused no<br />

significant inhibition of plasma, RBC, cerebrum, or cerebellum cholinesterase activities (Moreno 1989).<br />

No signs of toxicity were observed in this study.<br />

In the Boyes et al. (1999) study that was briefly described under Ocular Effects, the authors also<br />

examined the effects of <strong>malathion</strong> on visual evoked potentials (VEP) in Long-Evans rats by implanting<br />

the animals with cranial electrodes <strong>for</strong> recording of VEP. The amount of <strong>malathion</strong> applied to the eye<br />

resulted in approximate doses of 500 mg/kg/day <strong>for</strong> 4 weeks. Treatment with <strong>malathion</strong> had no<br />

significant effect on the amplitude or phase, or the first harmonic of the VEPs. During the study, there<br />

were no signs of cholinergic activation. Examination of the retina <strong>and</strong> optic nerve 42 days after<br />

termination of the study revealed no treatment-related alterations.<br />

The highest NOAEL values <strong>and</strong> all reliable LOAEL values <strong>for</strong> neurological effects in each species <strong>and</strong><br />

duration category are recorded in Table 3-3.<br />

3.2.3.5 Reproductive Effects<br />

No studies were located regarding reproductive effects in humans following dermal exposure to<br />

<strong>malathion</strong>. A study in male guinea pigs reported a decrease in absolute testes weight following<br />

application of 400 mg/kg/day of <strong>malathion</strong> (98% pure) in acetone to the skin <strong>for</strong> 30 days; however, doses

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