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

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a<br />

Key to<br />

figure<br />

61<br />

62<br />

63<br />

64<br />

65<br />

Species<br />

(Strain)<br />

Systemic<br />

Rat<br />

(Sprague-<br />

Dawley)<br />

Exposure/<br />

Duration/<br />

Frequency<br />

(Specific Route)<br />

6 mo<br />

ad libitum<br />

(W)<br />

Rat 13 wk<br />

(Fischer- 344)<br />

ad libitum<br />

(F)<br />

Rat<br />

(albino)<br />

Mouse<br />

(Hissar)<br />

Dog<br />

(Beagle)<br />

15 wk<br />

1x/d<br />

(GO)<br />

Immuno/ Lymphoret<br />

66 Rat<br />

8 -22 wk<br />

(Wistar)<br />

ad libitum<br />

(F)<br />

System<br />

Hemato<br />

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

NOAEL<br />

(mg/kg/day)<br />

Less Serious<br />

LOAEL<br />

Serious<br />

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

0.15 F (prolonged prothrombin <strong>and</strong><br />

partial thromboplastin times)<br />

Hepatic 0.15 F (hepatocyte degeneration)<br />

Bd Wt<br />

Bd Wt<br />

Endocr<br />

0.15 F<br />

700<br />

10 (significant decrease in serum<br />

cortizol <strong>and</strong> aldosterone levels,<br />

<strong>and</strong> congestion in zona<br />

reticularis of adrenal gl<strong>and</strong>s in<br />

both sexes)<br />

(continued)<br />

1399 F (final body weight reduced 50%<br />

relative to controls)<br />

Reference<br />

Chemical Form<br />

Lox <strong>and</strong> Davis 1983<br />

NCI 1979a<br />

Ozmen <strong>and</strong> Akay 1993<br />

3 -12 wk Banerjee et al. 1998<br />

Hepatic 10.5 M 21 M (increased relative liver weight)<br />

(F)<br />

Bd Wt<br />

21 M<br />

28 d Fischer 1988<br />

Gastro<br />

125 (diarrhea)<br />

(C)<br />

2.3 M<br />

5.8 M (reduced humoral <strong>and</strong><br />

cell-mediated immune<br />

responses to antigens)<br />

Banerjee et al. 1998

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