Human Reproduction, Vol 13, 1429-1436, Copyright © 1998 by Oxford University Press
J Twigg, N Fulton, E Gomez, DS Irvine and RJ Aitken
Exposure of human spermatozoa to nicotinamide adenine dinucleotide
phosphate (NADPH) resulted in the dose dependent generation of reactive
oxygen species (ROS) which, at a critical level of intensity, induced lipid
peroxidation, DNA damage and a dramatic decline of sperm motility. This
system was then used as a model for screening the ability of different
antioxidants to combat oxidative stress created through the excessive
intracellular generation of toxic oxygen products of metabolism. A variety
of antioxidants that has previously been shown to be protective against
extracellularly derived oxidants (e.g. superoxide dismutase, catalase,
vitamin E, hypotaurine) were ineffective in this system. Albumin, however,
could provide complete protection against NADPH induced oxidative stress
via mechanisms that did not involve the suppression of the lipid
peroxidation cascade but rather the inactivation of lipid peroxides
generated during this process. Albumin did not protect against DNA damage
induced by NADPH but was extremely effective at preventing DNA
fragmentation arising from the suppression of glutathione peroxidase
activity with mercaptosuccinate. These studies emphasize that the design of
clinically effective antioxidant treatments will depend, critically, upon
the source of the oxidative stress. For cases involving excessive
intracellular ROS generation, albumin appears to be an important means of
neutralizing lipid peroxide-mediated damage to the sperm plasma membrane
and DNA.
ARTICLES
Analysis of the impact of intracellular reactive oxygen species generation on the structural and functional integrity of human spermatozoa: lipid peroxidation, DNA fragmentation and effectiveness of antioxidants
MRC Reproductive Biology Unit, Edinburgh, UK.
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