Literature DB >> 18325884

Protective effect of antioxidant supplementation in sperm-preparation medium against oxidative stress in human spermatozoa.

H J Chi1, J H Kim, C S Ryu, J Y Lee, J S Park, D Y Chung, S Y Choi, M H Kim, E K Chun, S I Roh.   

Abstract

BACKGROUND: Oxidative stress induced by reactive oxygen species (ROS) is associated with an impaired fertilization ability of spermatozoa. We investigated the effects of adding antioxidants to a sperm preparation medium on the functional parameters of the spermatozoa.
METHODS: Spermatozoa were washed with Ham's F-10 media containing the antioxidants, ethylenediaminetetraacetic acid (EDTA) and catalase, at various concentrations, and then the ROS levels in sperm suspensions, and the forward motility, acrosome reaction, DNA integrity and lipid peroxidation of the spermatozoa were assessed.
RESULTS: The ROS levels were significantly lower in sperm suspensions washed with the antioxidants (196 approximately 312 rlu; relative light units) than in control sperm (604 rlu, P < 0.05). The addition of 10 microM EDTA to the sperm preparation medium significantly improved the motility of the spermatozoa compared with the control group, the groups containing EDTA at other concentrations and the groups containing catalase. Catalase significantly increased the acrosome reaction rate of the spermatozoa. Both EDTA and catalase significantly decreased the DNA fragmentation rate of the spermatozoa. However, the antioxidants did not reduce lipid peroxidation.
CONCLUSIONS: Supplementing sperm preparation medium with EDTA or catalase significantly improved the overall functional parameters of the spermatozoa by reducing the ROS levels.

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Year:  2008        PMID: 18325884     DOI: 10.1093/humrep/den060

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  21 in total

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9.  Protective effects of in vitro treatment with zinc, d-aspartate and coenzyme q10 on human sperm motility, lipid peroxidation and DNA fragmentation.

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10.  Evaluation of ebselen supplementation on cryopreservation medium in human semen.

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