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

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MALATHION 66<br />

3. HEALTH EFFECTS<br />

1965; Crowley <strong>and</strong> Johns 1966; Healy 1959; Rivett <strong>and</strong> Potgieter 1987). These effects result from the<br />

stimulation of parasympathetic autonomic postganglionic nerves by organophosphates <strong>and</strong> the lack of<br />

reporting of these effects in the additional studies reviewed most likely reflects incomplete reporting<br />

rather than the absence of gastrointestinal effects.<br />

Diarrhea was observed in beagle dogs treated with 125 mg/kg/day (the lowest dose tested) <strong>malathion</strong><br />

(92.4% pure) in gelatin capsules <strong>for</strong> 28 days (Fischer 1988). Rats administered <strong>malathion</strong> (22 mg/kg/day)<br />

by gavage in a mixture of alcohol <strong>and</strong> water <strong>for</strong> 6 days suffered diarrhea (Simionescu et al. 1977).<br />

Diarrhea is a common muscarinic sign of organophosphate pesticide intoxication. Rats treated with<br />

gavage doses of 130 mg/kg/day of <strong>malathion</strong> (unspecified purity) <strong>for</strong> 1–2 weeks showed gastrointestinal<br />

alterations described by the authors as catarrhal changes (Piramanayagam <strong>and</strong> Manohar 2002).<br />

In<strong>for</strong>mation from a single dose study in rats suggested that <strong>malathion</strong> may alter gastrointestinal<br />

absorption. Absorption was examined in an isolated portion of the intestines from male Wistar rats<br />

48 hours after administration of a single gavage dose of 1,000 mg/kg/day of technical <strong>malathion</strong> (purity<br />

unspecified) (Chowdhury et al. 1980). Absorption of glucose <strong>and</strong> glycine were reduced <strong>and</strong> the activities<br />

of some brush border enzymes were depressed in the <strong>malathion</strong>-treated rats. In a subsequent study from<br />

the same group in which rats were treated <strong>for</strong> 45 days with 50 mg/kg/day <strong>malathion</strong>, the authors found<br />

that treatment with <strong>malathion</strong> significantly increased the absorption of glucose, phenylalanine, <strong>and</strong> lysine,<br />

but not glycine, <strong>and</strong> increased brush border enzyme activities (Wali et al. 1984).<br />

No gastrointestinal effects were reported in Osborne-Mendel rats administered up to approximately<br />

622 mg/kg/day <strong>malathion</strong> (95% pure) in the diet <strong>for</strong> 80 weeks or in B6C3F1 mice treated with up to<br />

2,980 mg/kg/day in the diet <strong>for</strong> 80 weeks (NCI 1978). However, male Fischer-344 rats administered<br />

166 mg/kg/day <strong>malathion</strong> (95% pure) or more in the diet <strong>for</strong> 103 weeks developed chronic inflammation<br />

of the stomach <strong>and</strong> stomach ulcers.<br />

Hematological Effects. Almost all of the case reports of oral ingestion of <strong>malathion</strong> described the<br />

results of laboratory tests conducted on the patients on or following admission to treatment centers. In<br />

most cases, these included complete <strong>and</strong> differential blood counts, which may or may have not deviated<br />

from the normal ranges. However, observed deviations are probably not unique to <strong>malathion</strong><br />

intoxication, or to organophosphates in general, but represent stress reactions (Aaron <strong>and</strong> Howl<strong>and</strong> 1998).<br />

For example, it is not uncommon to find high hematocrit secondary to hemoconcentration due to large<br />

fluid losses (Aaron <strong>and</strong> Howl<strong>and</strong> 1998). There<strong>for</strong>e, a detailed discussion of specific alterations from the<br />

individual cases is of little utility.

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