Teratogenicity testing based on the interaction with a mutant allele.

V Bílá; V Kren

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PubMed · 1597253

Teratogenicity testing based on the interaction with a mutant allele.

V Bílá·V Kren

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Abstract

The system of congenic strains of the laboratory rat carrying the mutant allele lx which is determining the polydactyly-luxate syndrome (PLS) was used for testing teratogenicity of six compounds from different pharmacological groups (cyclophosphamide, cyadox, carbadox, imipramine, verapamil, TIA). The interaction of the mutant lx allele with cyclophosphamide was highly significant (P less than 0.001) involving both polydactyly and tibial hemimely. Significant interaction with the lx allele was also proved after cyadox and carbadox treatment when compared with lx allele penetrance in LEW/BN, +/1x heterozygotes (P less than 0.01 and 0.05). In accord with our previous experiments, the teratogenic activity of the compounds tested seems to be connected with the ability to interact with nucleic acid structure and/or function.

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Abnormalities, Drug-Induced Alleles Animals Anti-Bacterial Agents Cyclophosphamide Female Fetus Imipramine Male Mutagenicity Tests Rats Rats, Inbred Lew Verapamil Journal Article

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V Bílá, V Kren. 1992. Teratogenicity testing based on the interaction with a mutant allele.. https://pubmed.ncbi.nlm.nih.gov/1597253/

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