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

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MALATHION 85<br />

3. HEALTH EFFECTS<br />

hyperplasia was seen in B6C3F1 mice administered 1,490 mg/kg/day <strong>malathion</strong> (95% pure) <strong>for</strong> 80 weeks<br />

(NCI 1978).<br />

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

duration category are recorded in Table 3-2 <strong>and</strong> plotted in Figure 3-2.<br />

3.2.2.6 Developmental Effects<br />

No studies were located regarding developmental effects in humans following oral exposure to <strong>malathion</strong>.<br />

The developmental toxicity of <strong>malathion</strong> has been investigated primarily in rats, although some<br />

in<strong>for</strong>mation is also available in mice <strong>and</strong> rabbits.<br />

Embryotoxicity. In acute studies in rats, embryotoxicity was evident only in a study by Prabhakaran et al.<br />

(1993) who reported a reduction in the number of live fetuses per litter <strong>and</strong> reduced fetal weight in<br />

Sprague-Dawley rats treated with 500 mg/kg/day (only level tested) <strong>malathion</strong> (98% pure) on Gd 6, 10,<br />

<strong>and</strong> 14. It should be noted, however, that treated dams gained significantly less weight during pregnancy<br />

than controls. No embryotoxicity was observed in Wistar rats treated with 100 mg/kg/day <strong>malathion</strong><br />

(unspecified purity) on Gd 6–15 (Khera et al. 1978) or in Sprague Dawley rats treated with<br />

800 mg/kg/day <strong>malathion</strong> (94% pure) also on Gd 6–15 (Lochry 1989). Reduced fetal weight <strong>and</strong> crownrump<br />

length were seen in mice gavaged once on Gd 6 with 125 mg/kg <strong>malathion</strong> (unspecified purity) <strong>and</strong><br />

examined on Gd 15; however, no in<strong>for</strong>mation was provided on maternal effects (Asmatullah et al. 1993).<br />

Two studies in rabbits provided no evidence of embryotoxicity following gavage administration of<br />

100 mg/kg/day <strong>malathion</strong> on Gd 7–12 (Machin <strong>and</strong> McBride 1989a) or Gd 6–18 (Siglin 1985).<br />

Increased neonatal mortality (days 7 <strong>and</strong> 21 after birth) was reported in Wistar rats following maternal<br />

exposure to 240 mg/kg/day <strong>malathion</strong> (95% pure) in the diet <strong>for</strong> at least 5 months starting be<strong>for</strong>e mating<br />

(Kalow <strong>and</strong> Marton 1961). It is unclear, however, whether the rats were exposed during gestation.<br />

Furthermore, no in<strong>for</strong>mation was provided regarding maternal effects. Schroeder (1990) conducted a<br />

2-generation study in Sprague-Dawley rats in which the animals were administered <strong>malathion</strong> (94% pure)<br />

in the diet at various levels between 43 <strong>and</strong> 703 mg <strong>malathion</strong>/kg/day. The only developmental effect<br />

noticed was a decrease in body weight gain in pups from the F1A <strong>and</strong> F2B litter during the lactation<br />

period at parental doses of 394 mg/kg/day <strong>for</strong> males <strong>and</strong> 451 mg/kg/day <strong>for</strong> females. The corresponding<br />

NOAELs were 131 <strong>and</strong> 153 mg/kg/day. In this study, there were no significant effects on clinical signs,<br />

growth be<strong>for</strong>e mating, food consumption, or maternal weight gain during gestation.

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