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© 1992 Oxford University Press

research-article

Assessment of a Short-Term Reproductive and Developmental Toxicity Screen

MARTHA W. HARRIS, ROBERT E. CHAPIN1, ANN C. LOCKHART*, MICHAEL P. JOKINEN{dagger}, Janet D. Allen and Eric A. Haskins

Developmental and Reproductive Toxicology Group *Computer, Sciences Corporation NIEHS, Research Triangle Park, North Carolina 27709 {dagger}Chemical Carcinogenesis Branch NIEHS, Research Triangle Park, North Carolina 27709

Received October 7, 1991; accepted March 6, 1992

Short-term tests for reproductive and developmental toxicity are needed to provide preliminary data on the toxicity of chem icals about which little or no data exist. An ideal design would test all aspects of reproduction and identify the target process in a short time period. One potential design has been evaluated using four chemicals of varying reproductive/developmental toxicity. Swiss mice were mated for 3 days prior to chemical exposure to produce time-mated females for gestational exposure and to ascertain fertility of the untreated males. The group of time-mated females was treated during Gestation Days 8–14 and allowed to litter for observations through Postnatal Day (PND) 4. Endpoints observed included pup number and body weights on PND 0, 1, and 4 and number of uterine implantation sites on PND 4. A second group of females was dosed daily for 19 days. After 7 days, these females (n = 10/group) were cohabited with male mice who had been treated for 5 days prior to this second mating. Daily chemical dosing continued during the 5-day cohabitation. This second group of females was killed after 19 days of treatment and the number of live and dead fetuses and implantation sites was recorded. After 17 days of dosing, male mice were killed and the reproductive system evaluated by organ weights, total epididymal sperm counts and motility, and testicular histology. All four chemicals tested, boric acid, ethylene glycol, ethylene glycol monomethyl ether, and theophylline, were found to be toxic to development or reproduction when tested previously by conventional developmental toxicity or continuous breeding protocols. This short-term (21 day) design correctly identified three of these four chemicals as reproductive and developmental toxicants and distinguished the potent toxicants from the less effective compounds. This design can be used to prioritize chemicals for further study, or to delineate the relative toxicities of structurally related chemicals, and to identify the proper dose range for subsequent toxicity studies.


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