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
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Analysis of lipid peroxidation in human spermatozoa using BODIPY C11
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. Ironinduced 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.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
C. Ortega Ferrusola, L. Gonzalez Fernandez, B. Macias Garcia, C. Salazar-Sandoval, A. Morillo Rodriguez, H. Rodriguez Martinez, J.A. Tapia, and F.J. Pena Effect of Cryopreservation on Nitric Oxide Production by Stallion Spermatozoa Biol Reprod, December 1, 2009; 81(6): 1106 - 1111. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. G. Buffone, S. V. Verstraeten, J. C. Calamera, and G. F. Doncel High Cholesterol Content and Decreased Membrane Fluidity in Human Spermatozoa Are Associated With Protein Tyrosine Phosphorylation and Functional Deficiencies J Androl, September 1, 2009; 30(5): 552 - 558. [Abstract] [Full Text] [PDF] |
||||
![]() |
C Ortega Ferrusola, L Gonzalez Fernandez, J M Morrell, C Salazar Sandoval, B Macias Garcia, H Rodriguez-Martinez, J A Tapia, and F J Pena Lipid peroxidation, assessed with BODIPY-C11, increases after cryopreservation of stallion spermatozoa, is stallion-dependent and is related to apoptotic-like changes Reproduction, July 1, 2009; 138(1): 55 - 63. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Tremellen Oxidative stress and male infertility--a clinical perspective Hum. Reprod. Update, May 1, 2008; 14(3): 243 - 258. [Abstract] [Full Text] [PDF] |
||||
![]() |
H.J. Chi, J.H. Kim, C.S. Ryu, J.Y. Lee, J.S. Park, D.Y. Chung, S.Y. Choi, M.H. Kim, E.K. Chun, and S.I. Roh Protective effect of antioxidant supplementation in sperm-preparation medium against oxidative stress in human spermatozoa Hum. Reprod., May 1, 2008; 23(5): 1023 - 1028. [Abstract] [Full Text] [PDF] |
||||




