Comparison of results from mouse bone marrow chromosome aberration and micronucleus tests

1995 ◽  
Vol 25 (4) ◽  
pp. 302-313 ◽  
Author(s):  
M. D. Shelby ◽  
K. L. Witt
2003 ◽  
Vol 58 (11-12) ◽  
pp. 833-836
Author(s):  
Margarita Topashka-Ancheva ◽  
Rilka Taskova ◽  
Nedjalka Handjieva ◽  
Bozhanka Mikhova ◽  
Helmut Duddeck

Abstract The clastogenic effect of total dichloromethane, methanol and water extracts, four bioactive fractions and three individual constituents from Carthamus lanatus aerial parts were evaluated in mice by bone marrow chromosome aberration assay with mitomycin C as positive control. Significant differences in the percentage of aberrant mitosis of the extracts were observed. The dichloromethane extract exhibited a considerable clastogenic effect and the water extract a negligible one. Different types of chromosome aberrations and time-dependant effects for the active fractions and individual compounds were found.


2014 ◽  
Vol 7 (1) ◽  
pp. 923
Author(s):  
Laurie C Dolan ◽  
Hana Hofman-Hüther ◽  
Nicole Amann

2011 ◽  
Vol 31 (1) ◽  
pp. 78-85 ◽  
Author(s):  
Imen Ayed-Boussema ◽  
Karima Rjiba ◽  
Nourhène Mnasri ◽  
Amal Moussa ◽  
Hassen Bacha

Dimethoate (DM) is an organophosphate insecticide with numerous uses on field and agricultural crops and ornamentals. Data concerning DM-acute genotoxicity are controversial and knowledge on its delayed effect is limited. For this reason, we aimed to further explore DM genotoxicity resulting from subchronic intoxication of experimental mice. Thus, DM was administered to mice at doses ranging from 1 to 30 mg/kg body weight for a period of 30 consecutive days. There was a significant increase ( P < .05) in the frequency of micronucleated bone marrow cells following DM administration. Furthermore, the chromosome aberration assay revealed a significant increase in the percentage of chromosome abnormalities in a dose-dependent manner. Dimethoate was also found to induce significant DNA damage in mouse bone marrow cells as assessed by the comet assay. Altogether, our results showed that, after a subchronic exposure, DM was a genotoxic compound in experimental mice.


2018 ◽  
Vol 2018 ◽  
pp. 1-6 ◽  
Author(s):  
Jin-Seok Lee ◽  
Jung-Hyo Cho ◽  
Dong-Soo Lee ◽  
Chang-Gue Son

Myelophil, a combination of Astragali Radix and Salviae Radix, is one of the most commonly used remedies for disorders of Qi and blood in traditional Chinese medicine. Based on the clinical applications of these plants, in particular to pregnant woman, this study aimed to evaluate the genotoxic potential of an ethanol extract mixture of the above two herbs, called Myelophil. Following the Organization for Economic Cooperation and Development (OECD) Guideline methods, a genotoxicity test was conducted using a bacterial reverse mutation test with Salmonella typhimurium (TA98, TA100, TA1535, and TA1537) and Escherichia coli (WP2μvrA), an in vitro mammalian chromosome aberration test using a Chinese hamster ovary cell line (CHO-K1), and an in vivo mammalian erythrocyte micronucleus test using ICR mouse bone marrow. In the Ames test, for both types of mutations (base substitution and frameshift) under conditions with/without an S9 mix up to 5,000 μg/plate, Myelophil did not increase the number of revertant colonies of all S. typhimurium strains as well as E. coli strain. For both short (6 h) and long tests with/without S9 mix, the chromosome aberration test did not show any significant increase in the number of structural or numerical chromosome aberrations by Myelophil. In addition, no significant change in the number of micronucleated polychromatic erythrocytes or polychromatic erythrocytes was observed in the bone marrow of an ICR mouse administered Myelophil orally at 2,000 mg/kg/day for 2 days, respectively. These results are the first to provide experimental evidence that Myelophil, an ethanol extract mixture of Astragali Radix and Salviae Radix, has no risk of genotoxicity.


2008 ◽  
Vol 169 (6) ◽  
pp. 633-638 ◽  
Author(s):  
Ronald E. Carsten ◽  
Annette M. Bachand ◽  
Susan M. Bailey ◽  
Robert L. Ullrich

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