31.10.2012 Views

Toxicological Review for 2-Methylnaphthalene (CAS No. 91-57-6 ...

Toxicological Review for 2-Methylnaphthalene (CAS No. 91-57-6 ...

Toxicological Review for 2-Methylnaphthalene (CAS No. 91-57-6 ...

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

Table 1. Distribution of radioactivity in guinea pigs after oral administration of 2-[ 3 H]methylnaphthalene<br />

Tissue 3 hours 6 hours 24 hours 48 hours<br />

Gallbladder<br />

Kidney<br />

Liver<br />

Blood<br />

Lung<br />

Others (combined)<br />

Internal organs<br />

Blood<br />

Gastrointestinal contents<br />

Urine<br />

Feces<br />

Total recovery<br />

Source: Adapted from Teshima et al., 1983.<br />

20.2<br />

5.6<br />

1.7<br />

0.8<br />

0.7<br />

0.8<br />

µg of 3 H/g wet tissue<br />

7<br />

15.7<br />

7.6<br />

2.7<br />

0.7<br />

0.8<br />

1.1<br />

Percent of total administered dose<br />

1.4<br />

0.6<br />

27.9<br />

23.1<br />

0<br />

53<br />

2.1<br />

0.5<br />

20.2<br />

41.3<br />

0<br />

64.2<br />

0.4<br />

0.3<br />

0.2<br />

0.1<br />

0.1<br />

0.2<br />

0.1<br />

0.1<br />

3.1<br />

78.6<br />

10.8<br />

92.7<br />

Griffin et al. (1982) administered single intraperitoneal injections of 400 mg/kg [ 14 C]-2-<br />

methylnaphthalene to male C<strong>57</strong>BL/6J mice. Groups of 4 mice were sacrificed at 0.5, 1, 3, 6, 12, or 24<br />

hours after injection <strong>for</strong> measurement of radioactivity in fat, kidney, liver, and lung. Blood 2-<br />

methylnaphthalene concentrations decreased with a reported elimination half-life of 3 hours, indicative<br />

of rapid distribution to other tissues or elimination from the body. Peak tissue concentrations of 2-<br />

methylnaphthalene equivalents (nmol/mg wet weight) were attained about 1 hour after injection in the<br />

liver, 2 hours after injection in the fat, and 4 hours after injection in the kidney and the lung (Griffin et al.,<br />

1982). Peak concentrations were highest in fat (13 nmol/mg), followed by lower concentrations in liver<br />

(3.5 nmol/mg), kidney (2.9 nmol/mg), and lung (0.7 nmol/mg). The results demonstrate that 2-<br />

methylnaphthalene did not preferentially accumulate in the lung although the lung was the only site of<br />

toxicity. Histological examination found that the single 400 mg/kg dose induced bronchiolar necrosis<br />

(minimal to prominent sloughing of lining cells in the bronchiolar lumen as revealed by light microscopy)<br />

in all exposed mice (Griffin et al., 1982). <strong>No</strong> lesions were found in the liver or kidney of exposed mice<br />

at any time point. Consistent with the attainment of peak lung tissue concentration at 4 hours after<br />

injection, no lesions were evident until 8 hours after injection. The authors also evaluated distribution by<br />

measurement of irreversible binding of label from [ 14 C]-2-methylnaphthalene to various tissues over a<br />

dose (0, 50, 100, 300, and 500 mg/kg; intraperitoneal injection) and time course (1, 2, 4, 8, 12, and<br />

0.04<br />

0.1<br />

0.1<br />

0.1<br />

0.1<br />

0.1<br />

0.1<br />

0.1<br />

1.0<br />

72.2<br />

11.9<br />

85.2

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!