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© 1990 Oxford University Press

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Reproductive Effects of Diethylene Glycol and Diethylene Glycol Monoethyl Ether in Swiss CD-1 Mice Assessed by a Continuous Breeding Protocol

JACQUELINE WILLIAMS*, JERRY R. REEL{dagger},1, JULIA.D GEORGE{dagger} and JAMES C. LAMB, IV*,2

*Developmental and Reproductive Toxicology Group, National Toxicology Program. NIEHS P.O. Box 12233, Research Triangle Park, North Carolina 27709 {dagger}Chemistry and Life Sciences, Research Triangle Institute P.O. Box 12194, Research Triangle Park, North Carolina 27709

Received July 31, 1989; accepted December 1, 1989

Reproductive Effects of Diethylene Glycol and Diethylene Glycol Monoethyl Ether in Swiss CD-I Mice Assessed by a Continuous Breeding Protocol. WILLIAMS, J., REEL, J. R., GEORGE, J. D., AND LAMB, J. C, IV. (1990). Fundam. Appl. Toxicol. 14, 622–635. Diethylene glycol (DEG) and diethylene glycol monoethyl ether (DEGEE) were evaluated for reproductive toxic-ity in CD-I mice using a continuous breeding protocol. Compounds were administered in the drinking water at 0, 0.35, 1.75, and 3.5% w/v (DEG) or 0, 0.25, 1.25, and 2.5% w/v (DEGEE). Exposure of the breeding pairs to 3.5% DEG for 14 weeks produced statistically significant decreases in the number of litters per pair, live pups per litter, proportion of pups born alive, and live pup weight. There was also a significant increase in the cumulative days to litter and a significant decrease in the number of pairs producing the third, fourth, and fifth litters for the 3.5% DEG-exposed mice. A crossover mating trial of the Fo mice to determine the affected sex was inconclusive, but suggested that offspring development was compromised in females exposed to 3.5% DEG. Slight maternal (Fo) toxicity was noted for the 3.5% DEG group (7% decrease in body weight). The F, generation, at 3.5% DEG, had decreased body weights at birth and exhibited poor postnatal survival. At the intermediate dose of DEG, body weights of both sexes were depressed at weaning, at onset of mating, and at necropsy. However, no adverse effects on reproduction were observed. DEGEE had no effect on reproduction in the Fo or F, generation mice despite a 34% decrease in cauda epididymal sperm motility in the F1 males at 2.5% DEGEE. Other signs of toxicity observed in these F1 mice included increased relative liver weights. These data indicate that DEG is a reproductive toxicant in Swiss mice affecting fertility and reproductive performance, albeit at high doses (equivalent to 6.1 g/kg/day). However, its monoethyl derivative, DEGEE, is without adverse effects on fertility and reproductive performance.


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