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

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MALATHION 35<br />

3. HEALTH EFFECTS<br />

Studies in animals support the findings in humans regarding cholinesterase inhibition. Exposure of<br />

rabbits to 123 mg <strong>malathion</strong>/m 3 as an aerosol generated from a technical <strong>malathion</strong> <strong>for</strong>mulation<br />

(95% pure) <strong>for</strong> 6 hours inhibited plasma cholinesterase activity by 37% at 24 hours postexposure <strong>and</strong> 41%<br />

at 72 hours postexposure (Weeks et al. 1977). This exposure also resulted in inhibition of erythrocyte<br />

cholinesterase by 38, 48, <strong>and</strong> 48% at 24 hours, 72 hours, <strong>and</strong> 7 days postexposure, respectively. The<br />

NOAEL was 65 mg/m 3 . Exposure to an aerosol <strong>for</strong>mulation containing 6% <strong>malathion</strong> <strong>and</strong> a fuel oil<br />

mixture resulted in 38% inhibition of plasma cholinesterase with a 66 mg/m 3 concentration 72 hours after<br />

exposure <strong>and</strong> 71% inhibition with a 128 mg/m 3 concentration 10 minutes postexposure. With this<br />

<strong>for</strong>mulation, erythrocyte cholinesterase was inhibited 61 <strong>and</strong> 46% with the 128 mg/m 3 concentration<br />

10 minutes <strong>and</strong> 24 hours, respectively, postexposure. Exposure to the 6% <strong>for</strong>mulation caused lethality,<br />

but no signs of toxicity or deaths were seen among rabbits exposed to the 95% <strong>malathion</strong> <strong>for</strong>mulation. By<br />

comparing these results to those obtained after oral exposure in a parallel experiment, Weeks et al. (1977)<br />

estimated that it took 15–20 times more <strong>malathion</strong> by ingestion to cause an effect similar to that seen by<br />

inhalation. The NOAEL of 65 mg/m 3 was used to derive an intermediate inhalation MRL of 0.02 mg/m 3<br />

<strong>for</strong> <strong>malathion</strong>.<br />

In a 13-week study, Sprague-Dawley rats were exposed whole body to up to 2,010 mg/m 3 of <strong>malathion</strong><br />

(96.4% pure) 6 hours/day, 5 days/week (Beattie 1994). At termination, the effects on cholinesterase<br />

activities were found to be exposure concentration-related <strong>and</strong> effects on females seemed more<br />

pronounced that in males. Plasma cholinesterase activity was decreased 30% at 450 mg/m 3 <strong>and</strong> 70% at<br />

2,010 mg/m 3 in females, respectively. RBC cholinesterase activity was decreased 22 <strong>and</strong> 27% at<br />

450 mg/m 3 in males <strong>and</strong> females, respectively, <strong>and</strong> 43 <strong>and</strong> 44% at 2,010 mg/m 3 in males <strong>and</strong> females,<br />

respectively. Brain cholinesterase activity was decreased 41% at 2,010 mg/m 3 in females. Excess<br />

salivation was seen mostly in rats from the high-exposure group, although it occurred sporadically in the<br />

other exposed groups.<br />

NOAEL <strong>and</strong> LOAEL values from the Beattie (1994), Golz (1959), <strong>and</strong> Weeks et al. (1977) studies are<br />

presented in Table 3-1 <strong>and</strong> plotted in Figure 3-1.<br />

3.2.1.5 Reproductive Effects<br />

Reproductive outcomes were investigated in a group of 7,450 women who were confirmed as pregnant<br />

during periods of <strong>malathion</strong> spraying to control an infestation by the Mediterranean fruit fly in the San

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