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Mol. Hum. Reprod. Advance Access originally published online on February 27, 2007
Molecular Human Reproduction 2007 13(4):203-211; doi:10.1093/molehr/gal119
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© The Author 2007. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Analysis of lipid peroxidation in human spermatozoa using BODIPY C11

R.John Aitken1,2, Jordana K. Wingate1, Geoffry N. De Iuliis1 and Eileen A. McLaughlin1

1 ARC Centre of Excellence in Biotechnology and Development, Discipline of Biological Sciences, University of Newcastle, NSW, Australia

2 To whom correspondence should be addressed at: FRSE, Discipline of Biological Sciences, The University of Newcastle, Callaghan NSW 2308, Australia. E-mail: jaitken{at}mail.newcastle.edu.au

Lipid peroxidation is known to be a major factor in the aetiology of defective sperm function. Although biochemical assays for this process exist, they are relatively insensitive and require large numbers of spermatozoa; a condition that cannot be met with many infertility specimens. Recently, a new approach for monitoring peroxidative damage has been introduced, involving the probe BODIPY (581/591) C11, which readily incorporates into cells and undergoes a spectral emission shift when attacked by reactive oxygen metabolites. We have examined the applicability of this probe as an indicator of oxidative stress in human sperm populations using flow cytometry as an end point. The measurement of peroxidation with BODIPY C11 demonstrated significant dependence on the presence of a ferrous ion promoter (P < 0.001), which was significantly enhanced in sperm recovered from low-density Percoll fractions (P < 0.05) and was particularly damaging to the sperm midpiece. Iron–induced radical formation was suppressed by ascorbate in a dose-dependent manner (P < 0.001) and could only be promoted by Fe(II) and Cu(II); nickel, zinc and Fe(III) were ineffective. The Fe(II)-promoted BODIPY C11 signal was significantly correlated with the measurement of reactive oxygen species generation with dihydroethidium. We conclude that BODIPY C11 is an extremely useful probe for indexing peroxidative damage in human spermatozoa.

Key words: BODIPY C11/human spermatozoa/lipid peroxidation/oxidative stress

Submitted on November 20, 2006; accepted on January 2, 2007.


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