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EBX01000000000000001213063 |
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220928 ||| eng |
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|a Test No. 422: Combined Repeated Dose Toxicity Study with the Reproduction/Developmental Toxicity Screening Test
|h Elektronische Ressource
|c Organisation for Economic Co-operation and Development
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|a Essai n° 422 : Étude combinée de toxicité à doses répétées et de dépistage de la toxicité pour la reproduction et le développement
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| 260 |
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|a Paris
|b OECD Publishing
|c 2015
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| 300 |
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|a 19 p
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| 653 |
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|a Environment
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| 710 |
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|a Organisation for Economic Co-operation and Development
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|a eng
|2 ISO 639-2
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| 989 |
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|b OECD
|a OECD Books and Papers
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|a /10.1787/9789264242715-en
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|a oecd-ilibrary.org
|u https://doi.org/10.1787/9789264242715-en
|x Verlag
|3 Volltext
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|a 363
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| 520 |
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|a This screening Test Guideline describes the effects of a test chemical on male and female reproductive performance. It has been updated with endocrine disruptor endpoints, in particular measure of anogenital distance and male nipple retention in pups and thyroid examination. The test substance is administered in graduated doses to several groups of males and females. Males should be dosed for a minimum of four weeks. Females should be dosed throughout the study, so approximately 63 days. Matings "one male to one female" should normally be used in this study. This Test Guideline is designed for use with the rat. It is recommended that each group be started with at least 10 animals of each sex. Generally, at least three test groups and a control group should be used. Dose levels may be based on information from acute toxicity tests or on results from repeated dose studies. The test substance is administered orally and daily. The results of this study include clinical observations, body weight and food/water consumption, oestrous cycle monitoring, offspring parameters observation/measurement, thyroid hormone measurement, as well as gross necropsy and histopathology. The findings of this toxicity study should be evaluated in terms of the observed effects, necropsy and microscopic findings. Because of the short period of treatment of the male, the histopathology of the testis and epididymus should be considered along with the fertility data, when assessing male reproductive effects
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