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. 2010 Nov;94(6):2359-61.
doi: 10.1016/j.fertnstert.2010.04.017.

Antioxidants, Oxyrase, and mitochondrial uncoupler 2,4-dinitrophenol improved postthaw survival of rhesus monkey sperm from ejaculates with low cryosurvival

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Antioxidants, Oxyrase, and mitochondrial uncoupler 2,4-dinitrophenol improved postthaw survival of rhesus monkey sperm from ejaculates with low cryosurvival

Qiaoxiang Dong et al. Fertil Steril. 2010 Nov.

Abstract

Various antioxidant strategies such as supplementation of antioxidants, limiting oxygen concentration with Oxyrase, and reducing reactive oxygen species through mild mitochondrial uncoupling had statistically significant beneficial effects on sperm cryopreservation from rhesus monkeys with low cryoresistant ejaculates. Individuals or species that have higher sensitivity to cryodamage may derive the most benefit from these treatments.

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Figures

Fig. 1
Fig. 1
Post-thaw motility of rhesus monkey sperm samples frozen in TEY-3% glycerol with additives (closed circles) of 200 U/ml superoxide dimutase (SOD), 200 U/ml catalase (CAT), 0.3 U/ml oxyrase, 10 mM vitamin E (VE), and dinitrophenol (DNP) at the concentration range of 0.01, 0.1, 1, 10, 50 μM vs. controls without these additives (open circles). Controls for VE and DNP additives were 0.1% ethanol solvent control. Males with low post-thaw motility in controls (less than 60% for SOD, CAT, and oxyrase or less than 50% for VE and DNP groups) were shown in Panel (a), and males with high post-thaw motility in controls (equal or above 60% for SOD, CAT, and oxyrase groups or 50% for VE and DNP groups) were shown in Panel (b). Asterisks indicate significant difference between controls and treatment groups.

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References

    1. Chatterjee S, Gagnon C. Production of reactive oxygen species by spermatozoa undergoing cooling, freezing, and thawing. Mol Reprod Dev. 2001;59:451–8. - PubMed
    1. Michael A, Alexopoulos C, Pontiki E, Hadjipavlou-Litina D, Saratsis P, Boscos C. Effect of antioxidant supplementation on semen quality and reactive oxygen species of frozen-thawed canine spermatozoa. Theriogenology. 2007;68:204–12. - PubMed
    1. Bilodeau JF, Chatterjee S, Sirard MA, Gagnon C. Levels of antioxidant defenses are decreased in bovine spermatozoa after a cycle of freezing and thawing. Mol Reprod Dev. 2000;55:282–8. - PubMed
    1. Marti E, Marti JI, Muino-Blanco T, Cebrian-Perez JA. Effect of the cryopreservation process on the activity and immunolocalization of antioxidant enzymes in ram spermatozoa. J Androl. 2008;29:459–67. - PubMed
    1. Thuwanut P, Chatdarong K, Techakumphu M, Axnér E. The effect of antioxidants on motility, viability, acrosome integrity and DNA integrity of frozen-thawed epididymal cat spermatozoa. Theriogenology. 2008;70:233–40. - PubMed

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