Maternal phenytoin administration affects DNA and protein synthesis in embryonic primary palates
- 1 December 1983
- journal article
- research article
- Published by Wiley in Teratology
- Vol. 28 (3) , 389-397
- https://doi.org/10.1002/tera.1420280310
Abstract
Recent studies have shown that phenytoin (Dilantin®) administration to pregnant A/J mice on day 10 causes reduced growth in embryonic primary palates. The current investigation concentrates on biochemical and autoradiographic changes toward the end of primary palate formation (gestational day 11), which coincides with the developmental period used for the previously conducted morphological studies. On gestational day 10, one group of pregnant A/J mice was injected intraperitoneally (IP) with 60 mg/kg phenytoin and the other group with vehicle. Twenty-three hours after phenytoin administration, all animals were injected (IP) with either [3H]-thymidine or [3H]-leucine. After one hour of incorporation, animals were sacrificed, embryos removed and placed in ice-cold Eagle's minimum essential medium containing 0.02% NaN3 for biochemical assay or fixed immediately in Bouin's solution for autoradiography. For biochemical analyses, palates and limb buds were removed, homogenized, TCA precipitated, lyophilized, and acid hydrolyzed. Examination of the data revealed that DNA synthesis in control palates was 3.8-fold greater than in primary palates from embryos of phenytoin-treated mothers. Results were similar for limb buds from control embryos and from embryos of phenytoin-treated mothers. Experiments utilizing [3H]-leucine indicated that protein synthesis was 2.6-fold greater in primary palates from phenytointreated mothers than in control primary palates. Similar results were obtained for protein synthesis in limb-bud tissue from controls and embryos of phenytoin-treated mothers. Autoradiographic data supported the biochemical findings. DNA synthesis in primary palates from embryos of phenytoin-treated mothers decreased 3-fold; protein synthesis increased 2.2-fold compared with control primary palates. Similar autoradiographic results were obtained from limb-bud tissue from embryos of phenytoin-treated mothers. The results indicate that DNA synthesis is decreased and protein synthesis is increased in embryonic primary palates from phenytoin-treated mothers. Similar changes in DNA and protein synthesis in embryonic limb buds indicate that phenytoin alterations are not limited to primary palates.This publication has 7 references indexed in Scilit:
- A MODIFIED NINHYDRIN REAGENT FOR THE PHOTOMETRIC DETERMINATION OF AMINO ACIDS AND RELATED COMPOUNDSPublished by Elsevier ,2021
- Maternal Hyperoxia Greatly Reduces the Incidence of Phenytoin-Induced Cleft Lip and Palate in A/J MiceScience, 1981
- Phenytoin (dilantin)‐induced cleft lip and palate in a/j mice: A scanning and transmission electron microscopic studyThe Anatomical Record, 1979
- 203 POLYAMINE AND NUCLEIC ACID ALTERATIONS FOLLOWING TERATOGENIC TREATMENT WITH DIPHENYLHYDANTOINPediatric Research, 1978
- Science and Art in Preparing Tissues Embedded in Plastic for Light Microscopy, with Special Reference to Glycol Methacrylate, Glass Knives and Simple StainsStain Technology, 1976
- Teratogenic Effects of Diphenylhydantoin in Swiss-Webster and A/J MiceExperimental Biology and Medicine, 1968
- Radiomimetic effects of a nitrogen mustard on survival, growth, protein and nucleic acid synthesis of mammalian cells in vitroExperimental Cell Research, 1963