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

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a<br />

Key to<br />

figure<br />

93<br />

94<br />

Species<br />

(Strain)<br />

Systemic<br />

Mouse<br />

(B6C3F1)<br />

Mouse<br />

(B6C3F1)<br />

Exposure/<br />

Duration/<br />

Frequency<br />

(Specific Route)<br />

80 wk<br />

ad libitum<br />

(F)<br />

18 mo<br />

ad libitum<br />

(F)<br />

95<br />

Neurological<br />

Rat<br />

2 yr<br />

(Fischer- 344)<br />

ad libitum<br />

(F)<br />

System<br />

Resp<br />

Cardio<br />

Gastro<br />

Musc/skel<br />

Hepatic<br />

Renal<br />

Endocr<br />

Dermal<br />

Table 3-2 Levels of Significant Exposure to Malathion - Oral<br />

NOAEL<br />

(mg/kg/day)<br />

2980<br />

2980<br />

2980<br />

2980<br />

2980<br />

2980<br />

2980<br />

Less Serious<br />

LOAEL<br />

Serious<br />

(mg/kg/day) (mg/kg/day)<br />

2980 (coughing <strong>and</strong> sneezing from<br />

week 72 until end of study)<br />

Bd Wt 1490 (>10% lower body weight than<br />

controls)<br />

Resp<br />

17.4 M<br />

167 F (increased incidence of<br />

non-neoplastic nasal lesions)<br />

Hepatic 167 F 1476 M (hepatocellular hypertrophy)<br />

Bd Wt 167 F 1476 M (14-20% decreased body<br />

weight)<br />

Other 167 F 1476 M (decreased food consumption)<br />

2 d M<br />

29 e<br />

M (29% inhibition of plasma<br />

cholinesterase)<br />

35 F (27% inhibition of RBC<br />

cholinesterase)<br />

(continued)<br />

359 M (64% inhibition of plasma<br />

cholinesterase)<br />

Reference<br />

Chemical Form<br />

NCI 1978<br />

Slauter 1994<br />

Daly 1996a

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