Metformin Improves Quality of Post-Thaw Canine Semen
Jérémy Grandhaye,
Agnieszka Partyka,
Zuzanna Ligocka,
Agata Dudek,
Wojciech Niżański,
Eric Jeanpierre,
Anthony Estienne,
Pascal Froment
Affiliations
Jérémy Grandhaye
INRAE UMR85 Physiologie de la Reproduction et des Comportements, 37380 Nouzilly, France
Agnieszka Partyka
Faculty of Veterinary Medicine, Department of Reproduction and Clinic of Farm Animals, Wroclaw University of Environmental and Life Sciences, Pl. Grunwaldzki 49, 50-366 Wroclaw, Poland
Zuzanna Ligocka
Faculty of Veterinary Medicine, Department of Reproduction and Clinic of Farm Animals, Wroclaw University of Environmental and Life Sciences, Pl. Grunwaldzki 49, 50-366 Wroclaw, Poland
Agata Dudek
Faculty of Veterinary Medicine, Department of Reproduction and Clinic of Farm Animals, Wroclaw University of Environmental and Life Sciences, Pl. Grunwaldzki 49, 50-366 Wroclaw, Poland
Wojciech Niżański
Faculty of Veterinary Medicine, Department of Reproduction and Clinic of Farm Animals, Wroclaw University of Environmental and Life Sciences, Pl. Grunwaldzki 49, 50-366 Wroclaw, Poland
Eric Jeanpierre
INRAE UMR85 Physiologie de la Reproduction et des Comportements, 37380 Nouzilly, France
Anthony Estienne
INRAE UMR85 Physiologie de la Reproduction et des Comportements, 37380 Nouzilly, France
Pascal Froment
INRAE UMR85 Physiologie de la Reproduction et des Comportements, 37380 Nouzilly, France
Sperm cryopreservation is an assisted reproductive technique routinely used in canine species for genetic conservation. However, during cryopreservation, the DNA damages are still elevated, limiting the fertilization rate. The present study was conducted to evaluate whether supplementation of canine semen extender with a molecule limiting the metabolic activities can improve the quality of frozen-thawed canine spermatozoa. We used metformin, known to limit the mitochondrial respiratory and limit the oxidative stress. Before and during the freezing procedure, metformin (50µM and 500µM) has been added to the extender. After thawing, sperm exposed to metformin conserved the same viability without alteration in the membrane integrity or acrosome reaction. Interestingly, 50µM metformin improved the sperm motility in comparison to the control, subsequently increasing mitochondrial activity and NAD+ content. In addition, the oxidative stress level was reduced in sperm treated with metformin improving the sperm quality as measured by a different molecular marker. In conclusion, we have shown that metformin is able to improve the quality of frozen-thawed dog semen when it is used during the cryopreservative procedure.