Genotoxic damage induced by isopropanol in germinal and somatic cells of Drosophila melanogaster
Isopropanol (isopropyl alcohol, 2-propanol, IPA) is a volatile solvent widely used in domestic or industrial environments and reported as innocuous in various test systems. The aim of this work was to search for in vivo genotoxic effects of IPA in Drosophila melanogaster, studying its ability to ind...
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| Autores principales: | , |
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2011
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| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13835718_v726_n2_p215_Palermo http://hdl.handle.net/20.500.12110/paper_13835718_v726_n2_p215_Palermo |
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| Sumario: | Isopropanol (isopropyl alcohol, 2-propanol, IPA) is a volatile solvent widely used in domestic or industrial environments and reported as innocuous in various test systems. The aim of this work was to search for in vivo genotoxic effects of IPA in Drosophila melanogaster, studying its ability to induce nondisjunction (ND) in females, sex linked recessive lethals (SLRL) in males, and somatic mutation and/or recombination (SMART) in larvae. Treatments were acute (60. min) and were administered via inhalation. IPA had low toxicity in adult flies (75% IPA mortality index, MI = 12.7% (females) and 2.6% (males)) and larvae (MI = 14.3%, 75% IPA). Female fertility was severely affected during the first 24 h (brood I, BI) after treatment, but, afterwards, control values were recovered. IPA induced a 50-fold increase of ND (%) in 24 h old females, and a six-fold rise in 4-5 d old BI offspring. Nondisjunction frequencies (%) in the offspring of broods II to V (24 h in each case) were similar to control values. IPA doses of 25% and 50% (v/v), tested in 24 h old females, showed a significant dose-dependent increase of ND(%)in BI only, with control values in subsequent broods. Flies gave normal offspring when kept in regular media for 24 h before mating. The eye spot test (SMART) showed a significant increase at 50% IPA (p<0.05, m = 2), but the response was not dose-dependent. IPA failed to induce SLRL in any of the spermatogenesis stages tested. These findings suggest that the main effect of IPA is to induce chromosomal malsegregation; IPA must be present at the resumption of M-phase I after fertilization, to exert these effects. The alcohol does not affect DNA directly, but perturbations of the nuclear membrane may be responsible for induction of ND. © 2011 Elsevier B.V. |
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