6533b82bfe1ef96bd128d75f
RESEARCH PRODUCT
Effect of sperm glutathione peroxidases 1 and 4 on embryo asymmetry and blastocyst quality in oocyte donation cycles
María José De Los SantosMarcos MeseguerNicolás GarridoAntonio PellicerCarlos SimónJosé Remohísubject
AdultMalemedicine.medical_specialtyGPX1Glutathione reductaseFertilization in VitroBiologyGPX4Andrologychemistry.chemical_compoundGlutathione Peroxidase GPX1PregnancymedicineHumansCells CulturedGynecologychemistry.chemical_classificationGlutathione PeroxidaseOocyte Donationurogenital systemGlutathione peroxidaseObstetrics and GynecologyEmbryoGlutathioneMiddle AgedEmbryo MammalianPhospholipid Hydroperoxide Glutathione PeroxidaseSpermatozoaSpermBlastocystReproductive MedicinechemistryFemaleEmbryo qualitydescription
Objective To prospectively determine the impact of concrete components of the sperm oxidative glutathione stress system in terms of enzymatic activity and mitochondrial RNA (mRNA) expression on embryo quality and reproductive outcome. Human spermatozoa use the glutathione system to inactivate reactive oxygen metabolites, and there is a close correlation between some components of the glutathione system and male fertility. However, very few data are published regarding this system in sperm cells and its effect on fertilization ability and embryo development in human beings. Design An oocyte-donation model, used to homogenize the female factor. Setting University-affiliated private IVF setting. Patient(s) Semen samples from infertile males (n = 43) of couples undergoing oocyte-donation cycles (n = 43). Intervention(s) None. Main Outcome Measure(s) Gene expression and activity of glutathione peroxidases (GPXs) 1 and 4, glutathione reductase, and intracellular glutathione (GSH) by fluorescent quantitative polymerase chain reaction and spectrophotometry, respectively. Result(s) Fertilization rate, pronuclear number, asymmetry, and pronuclear body distribution were not correlated with any sperm glutathione parameters that were considered. When day 3 embryo parameters were evaluated, only GPX4 mRNA expression in sperm cells was statistically significantly lower when asymmetric embryos were observed. Also, worst embryo development and morphology on day 5 was statistically significantly correlated with lower sperm GPX1 activity (101.07 vs. 258.8 IU/mg protein). Glutathione system analysis in fresh sperm was not statistically significantly different in patients achieving pregnancy compared with those who not, and we did not find any correlation with implantation rate. Conclusion(s) We have been able to correlate embryo morphology on day 3 with the sperm expression of GPX family members. The results indicate that sperm-derived mRNA may condition human embryo quality and persist even to blastocyst stage. The correlation of the sperm GPX family mRNA expression with embryo health appears quite promising for discovery of molecular causes of male infertility.
year | journal | country | edition | language |
---|---|---|---|---|
2005-10-26 | Fertility and Sterility |