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

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MALATHION 74<br />

3. HEALTH EFFECTS<br />

Metabolic Effects. The only study that specifically reported metabolic effects was that of Zivot et al.<br />

(1993) in which severe metabolic acidosis was observed in an 80-year-old woman who ingested an<br />

unspecified, but fatal, amount of <strong>malathion</strong>. Anion gap acidosis is common in organophosphate<br />

poisoning from poor tissue perfusion (Aaron <strong>and</strong> Howl<strong>and</strong> 1998). No relevant in<strong>for</strong>mation was found in<br />

animal studies.<br />

Other Systemic Effects. The incidence of pancreatic involvement in <strong>malathion</strong> intoxication was<br />

investigated in 75 patients who ingested unspecified amounts of liquid <strong>for</strong>mulations of the pesticide<br />

(Dagli <strong>and</strong> Shaikh 1983). Serum amylase levels over 500 units (normal range 80–200 units) in<br />

10 patients suggested that these patients had acute pancreatitis, whereas milder elevations in 37 patients<br />

suggested mild pancreatic dysfunction; all amylase levels returned to within normal values within 3 days<br />

following treatment <strong>for</strong> organophosphate poisoning. Dagli <strong>and</strong> Shaikh (1983) stated that the occurrence<br />

of pancreatitis was the result of functional ductal obstruction caused by an increase in exocrine flow rate,<br />

which is consistent with activation of muscarinic receptors in the pancreas by <strong>malathion</strong>. The occurrence<br />

of pancreatic involvement could not be confirmed by surgery or autopsy because all patients recovered.<br />

Hyperglycemia <strong>and</strong>/or glucosuria were reported in several cases of acute <strong>malathion</strong> poisoning (Crowley<br />

<strong>and</strong> Johns 1966; Dive et al. 1994; Healy 1959; Zivot et al. 1993). The exact cause of these findings is<br />

unknown.<br />

As previously mentioned, there are some oral studies in animals that provided in<strong>for</strong>mation on food <strong>and</strong>/or<br />

water consumption during administration of <strong>malathion</strong>. For example, decreased food intake was reported<br />

in rats given 163 mg/kg/day <strong>malathion</strong> in the diet <strong>for</strong> 7 days (Ojha et al. (1992) <strong>and</strong> in water intake when<br />

<strong>malathion</strong> was administered in the drinking water at a target dose of 95 mg/kg/day <strong>for</strong> 14 days (Lox<br />

1985). A chronic-duration study reported a significant decrease in food consumption in rats fed<br />

approximately 1,476 mg/kg/day <strong>malathion</strong> in the diet <strong>for</strong> 18 months (Slauter 1994). These effects may<br />

reflect aversion to the taste or smell of the diet <strong>and</strong> have no <strong>toxicological</strong> significance. There is no<br />

evidence that <strong>malathion</strong> may affect food utilization.<br />

3.2.2.3 Immunological <strong>and</strong> Lymphoreticular Effects<br />

No in<strong>for</strong>mation was located regarding immunological effects in humans following oral exposure to<br />

<strong>malathion</strong>. In animals, the effects of <strong>malathion</strong> on the immune system have been examined in numerous

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