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RATL: A Database of Reptile and Amphibian Toxicology Literature

RATL: A Database of Reptile and Amphibian Toxicology Literature

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Table 5 - FETAX Studies - 9<br />

Contaminant a Contaminant<br />

b<br />

Concentration<br />

b<br />

LC50 EC50 b<br />

TI d<br />

MCIG d<br />

NOEL d<br />

LOEL d<br />

Effects/Notes de<br />

Reference k<br />

DMSO<br />

1.77 - 1.24 - 1.4 1.3 - 1.5 1.3 - 1.7 Results from 3 trials. Rayburn et al. 1991b<br />

(dimethylsulfoxide)<br />

1.86<br />

DMSO<br />

0, 1-1.2% v/v 1.0% v/v DMSO potentiated the lethal effect <strong>of</strong> Rayburn et al. 1991a<br />

(dimethylsulfoxide)<br />

both teratogens but did not alter<br />

significantly the rate <strong>of</strong> malformation.<br />

EC25(96) = 1.2% v/v. There were<br />

additive effects for growth for all<br />

solvents with the teratogens.<br />

DMSO<br />

0.25-2.0% v/v 1.92% 1.57% 1.2, 1.24<br />

1.0% v/v<br />

Least toxic or teratogenic solvent Dresser et al. 1992<br />

(dimethylsulfoxide)<br />

(trials (trials (trials<br />

(trials<br />

examined. NOELs for mortality <strong>and</strong><br />

pooled) pooled) separate)<br />

separate)<br />

length were: 1.75, 1.5% v/v (mortality),<br />

(malform)<br />

1.25, 1.0% v/v (length).<br />

DPH (diphenylhydantoin) up 74.5 up 32.4 to reduced<br />

Both p-HPPH <strong>and</strong> m-HPPH<br />

Fort <strong>and</strong> Bantle 1990b<br />

to126.4 62.9 mg/L 1.2 fold<br />

(hydroxylated metabolites) were much<br />

mg/L<br />

less developmentally toxic than DPH.<br />

emetine 0.7 µg/mL No significant difference occurred in<br />

mortality resulting from any treatment.<br />

Administration alone resulted in 28.9%<br />

malformation <strong>of</strong> survivors.<br />

Coadministration <strong>of</strong> caffeine,<br />

theophylline <strong>and</strong> theobromine<br />

significantly increased the incidence <strong>of</strong><br />

malformations.<br />

Dawson <strong>and</strong> Bantle 1987a<br />

ethanol 1.44 - 1.01 - 1.33 - 0.6 - 1.0 Dawson <strong>and</strong> Bantle 1987b<br />

1.95 1.20 1.88<br />

ethanol 0.25-1.7% v/v 1.58,1.44 1.04% v/v 1.42,<br />

1.00, 0.75<br />

Most teratogenic solvent tested. NOEL Dresser et al. 1992<br />

% v/v (pooled 1.50<br />

%v/v<br />

for mortality <strong>and</strong> length were also<br />

(trials trials)<br />

calculated (1.25 % v/v <strong>and</strong> < 0.25% v/v,<br />

separate)<br />

respectively).<br />

ethidium bromide 50 (47- 35 (29-43) 1 mg/L Only a slight teratogenic risk. Growth was Courchesne <strong>and</strong> Bantle 1985<br />

54) mg/L mg/L<br />

the most sensitive endpoint measured.<br />

EC50 (96 h) for swimming ability = 50<br />

mg/L. Min conc. to inhibit development<br />

= 50 mg/L.<br />

ethylnitrosurea 0.29 0.05 5.8 Inactivated ENU (evaluated by different Bantle et al. 1989b<br />

mg.mL mg/mL<br />

operator) resulted in LC50 <strong>of</strong> 0.25<br />

mg/mL <strong>and</strong> EC50 <strong>of</strong> 0.052 mg/mL.<br />

fenthion 2.61 mg/L 0.002<br />

mg/L<br />

Tadpole. Channing 1998

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