METABOLIC-ACTIVATION OF 4 DRUGS IN THE EYE MOSAIC ASSAY MEASURING PRINCIPALLY MITOTIC RECOMBINATION IN DROSOPHILA-MELANOGASTER - DIFFERENCES IN STRAIN SUSCEPTIBILITY AND ROUTE OF EXPOSURE

Citation
R. Rodriguezarnaiz et Jh. Aranda, METABOLIC-ACTIVATION OF 4 DRUGS IN THE EYE MOSAIC ASSAY MEASURING PRINCIPALLY MITOTIC RECOMBINATION IN DROSOPHILA-MELANOGASTER - DIFFERENCES IN STRAIN SUSCEPTIBILITY AND ROUTE OF EXPOSURE, MUTATION RESEARCH, 305(2), 1994, pp. 157-163
Citations number
25
Categorie Soggetti
Genetics & Heredity",Toxicology
Journal title
ISSN journal
00275107
Volume
305
Issue
2
Year of publication
1994
Pages
157 - 163
Database
ISI
SICI code
0027-5107(1994)305:2<157:MO4DIT>2.0.ZU;2-3
Abstract
One mycotoxin and three therapeutic drugs widely used in developing co untries were examined for genotoxic activity by means of w/w + somatic recombination assay. Streptozotocin (SZ), an antibiotic antineoplasti c agent, gave a frequency of light spots almost one order of magnitude higher than those obtained with the carcinogen mycotoxin sterigmatocy stin (STC), the antiprotozoal and antimicrobial metronidazole (MNZ), a nd the antifungal griseofulvin (GF). Thus the order of response was SZ >STC>MNZ>GF. Chronic treatment turned out to be the better route of ex posure for these genotoxins when compared with surface treatment. The performance of the insecticide-resistant strain Hikone-R was better th an that of the wild genotype LS (Leiden Standard). The positive test r esults obtained with all four chemicals showed that the P450 system of Drosophila is capable of metabolizing these genotoxins into electroph ilic intermediates.