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Chromosome aberrations in bone marrow cells of rats treated with MTBE
Iman Abd El-Moneim Darwish1, Sahar Abd El-Razik Mosallam2
1Zoology Department,Women's College for Arts, Science and Education, Ain Shams University, Cairo, Egypt.
Abstract:
In the present study, genotoxic effect of methyl tert butyl ether MTBE was analyzed by measuring chromosomal aberrations (CAs) in bone marrow cells of rats. Rats administered MTBE orally at 800, 1600mg/kg/day in corn oil for 14 and 28 consecutive days. Control rats received injection of distilled water. An additional two groups of rats received corn oil and served as vehicle controls. Treatment of corn oil for 14 and 28 days failed to induce chromosomal aberrations. The highest percentage of chromosomal aberrations was produced by the two tested dose 14 days after treatment. The most structural aberrations were Robertsonion translocations, deletion, dicentric, end to end association while, ring, acentric fragment and gaps were rare. The present results indicate that MTBE is harmful to mammalian genetic material.
Insights
Methyl tert-butyl ether (MTBE) exposure caused significant genotoxic effects, leading to chromosomal aberrations in rat bone marrow cells. These findings highlight MTBE
Area of Science:
- Environmental toxicology
- Genetics and heredity
- Mammalian cell biology
Background:
- Methyl tert-butyl ether (MTBE) is a fuel additive with potential environmental and health concerns.
- Assessing the genotoxicity of MTBE is crucial for understanding its impact on mammalian systems.
Purpose of the Study:
- To evaluate the genotoxic potential of MTBE by examining chromosomal aberrations (CAs) in rat bone marrow.
- To determine the dose-dependent and time-dependent effects of MTBE exposure on genetic material.
Main Methods:
- Rats were orally administered MTBE at doses of 800 and 1600 mg/kg/day for 14 and 28 consecutive days.
- Chromosomal aberrations in bone marrow cells were analyzed.
- Control groups received distilled water or corn oil (vehicle control).
Main Results:
- MTBE administration significantly increased the percentage of chromosomal aberrations in rat bone marrow cells.
- The highest incidence of CAs was observed 14 days after treatment at both tested doses.
- Common structural aberrations included Robertsonian translocations, deletions, and dicentric chromosomes; ring chromosomes, acentric fragments, and gaps were rare.
Conclusions:
- MTBE exhibits genotoxic effects in mammals, evidenced by its ability to induce chromosomal aberrations.
- The study indicates that MTBE is harmful to mammalian genetic material, necessitating further investigation into its long-term health implications.
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