Abstract
The comet assay was performed on mouse and human spermatozoa to examine the effect of alkaline DNA unwinding time. The spermatozoa were treated in vitro with the DNA-damaging agents, methyl methanesulfonate (MMS) or hydrogen peroxide (H 2 O 2), and then embedded in agarose gel on glass slides. The slides were immersed in alkaline solution (pH13) for 1, 5, 10 and 20min, and then subjected to the electrophoresis under neutral conditions. In mouse spermatozoa, comet tails seen in solvent controls became brighter and longer as the alkaline DNA unwinding time increased. However, in the MMS-treated mouse spermatozoa, a smaller difference in the damage from that in the solvent control was seen with time within a dose. DNA damage induced by H 2 O 2 could also be detected accurately after alkali treatment for 1-20min. In human spermatozoa, DNA damage induced by MMS and H 2 O 2 could be detected in a dose-dependent manner after alkali treatment for 1min. The ability of the comet assay to detect DNA damage was not adversely affected by the short period (1min) of the alkaline DNA unwinding time. © 2011 AJA, SIMM & SJTU. All rights reserved.
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Kusakabe, H., & Tateno, H. (2011). Shortening of alkaline DNA unwinding time does not interfere with detecting DNA damage to mouse and human spermatozoa in the comet assay. Asian Journal of Andrology, 13(1), 172–174. https://doi.org/10.1038/aja.2010.105
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