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

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MALATHION 65<br />

3. HEALTH EFFECTS<br />

effects were observed in mice from the low-dose group administered approximately 1,490 mg<br />

<strong>malathion</strong>/kg/day. Another long-term study (18 months) in mice reported an increased incidence of<br />

nonneoplastic nasal lesions in female B6C3F1 mice treated with 96.4% pure <strong>malathion</strong> in the diet at<br />

167 mg/kg/day <strong>and</strong> in males <strong>and</strong> females at approximately 1,500 mg/kg/day (Slauter 1994). These<br />

lesions were characterized as exudate, suppurative, increased gl<strong>and</strong>ular secretion, olfactory atrophy, <strong>and</strong><br />

olfactory respiratory metaplasia. No such lesions were seen in animals treated with about 20 mg/kg/day<br />

of <strong>malathion</strong> or less.<br />

Cardiovascular Effects. Cardiovascular effects were observed in almost all reported cases of<br />

<strong>malathion</strong> poisoning (Crowley <strong>and</strong> Johns 1966; Dive et al. 1994; Healy 1959; Jušić <strong>and</strong> Milić 1978;<br />

Monje Argiles et al. 1990; Namba et al. 1970; Rivett <strong>and</strong> Potgieter 1987; Zivot et al. 1993). In general,<br />

signs <strong>and</strong> symptoms on admission included bradycardia <strong>and</strong> low blood pressure as expected from vagal<br />

stimulation. Several cases also observed atrio-ventricular conduction disturbances within a few days after<br />

ingestion of the pesticide (Crawley <strong>and</strong> Johns 1966; Dive et al. 1994; Monje Argiles et al. 1990). Doses<br />

estimated in these cases ranged from 214 to 2,117 mg/kg. In contrast, Choi et al. (1998) reported a<br />

normal electrocardiogram <strong>and</strong> chest x-ray per<strong>for</strong>med in the emergency room in a woman who ingested<br />

approximately 1,071 mg/kg <strong>malathion</strong>.<br />

Tachycardia was reported in many Wistar rats treated with about 593 mg/kg/day of <strong>malathion</strong><br />

(unspecified purity) in the diet <strong>for</strong> 7 days, but not in those treated with ≤411 mg/kg/day <strong>malathion</strong> (Ojha<br />

et al. 1992). Tachycardia may be the result of cholinergic stimulation of parasympathetic <strong>and</strong><br />

sympathetic autonomic ganglia. Administration of gavage doses of 390 mg <strong>malathion</strong>/kg/day<br />

(unspecified purity) <strong>for</strong> 1–2 weeks to rats caused focal hemorrhage in the heart (Piramanayagam <strong>and</strong><br />

Manohar 2002). A single gavage dose of 1,950 mg/kg of <strong>malathion</strong> (95% pure), the only dose level<br />

tested, caused congestion <strong>and</strong> hemorrhage in the hearts of male Wistar rats 2 days after dosing, females<br />

were not tested (Piramanayagam et al. 1996). Although the authors did not specifically mention the heart,<br />

they stated that by day 12 after dosing, almost all organs examined appeared normal.<br />

No adverse cardiovascular effects were reported in long-term dietary studies in rats (up to 622 mg<br />

<strong>malathion</strong>/kg/day) (NCI 1978, 1979a) <strong>and</strong> mice (up to 2,980 mg <strong>malathion</strong>/kg/day) (NCI 1978; Slauter<br />

1994).<br />

Gastrointestinal Effects. Abdominal cramping, diarrhea, nausea, <strong>and</strong> vomiting were common signs<br />

<strong>and</strong> symptoms observed following ingestion <strong>malathion</strong> in some of the reports available (Amos <strong>and</strong> Hall

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