Effect of zinc supplementation during cryopreservation on post-thaw chicken semen parameters and fertility

The present study evaluated supplementation of zinc from different sources during chicken semen cryopreservation on post-thaw semen quality and fertility. Adult White Leghorn chicken semen was cryopreserved using 4% dimethyl sulfoxide (DMSO) in Sasaki diluent (SD). In the semen cryomixture zinc oxide (6.25 and 12.5 µM) and zinc sulphate (100 and 200 µM) was added and cryopreserved. The plastic semen straws were thawed at 5°C for 100 sec and samples were evaluated for sperm motility, live, abnormal and acrosome intact sperm. The lipid peroxidation in the seminal plasma was evaluated. The semen cryopreservation and evaluation were repeated on six occasions. Fertility of the zinc supplemented semen was evaluated by inseminating into White Leghorn hens. Zinc supplementation did not affect any of the post-thaw sperm parameters. The lipid peroxidation and fertility were similar between the treatments.  In conclusion, supplementation of zinc as zinc oxide or zinc sulphate during chicken semen cryopreservation does not affect post-thaw semen parameters or fertility.

[1]  M. Sharafi,et al.  The effect of zinc oxide on rooster semen cryopreservation , 2020, British poultry science.

[2]  M. Shanmugam,et al.  Effect of supplementing vitamin E analogues on post-thaw semen parameters and fertility in chicken , 2019, British poultry science.

[3]  P. Sutovsky,et al.  Zinc: A Necessary Ion for Mammalian Sperm Fertilization Competency , 2018, International journal of molecular sciences.

[4]  Diana S Chu Zinc: A small molecule with a big impact on sperm function , 2018, PLoS biology.

[5]  A. Shahat,et al.  Impact of supplementation of semen extender with antioxidants on the quality of chilled or cryopreserved Arabian stallion spermatozoa. , 2017, Cryobiology.

[6]  M. Sharafi,et al.  Orally administered Chrysin improves post‐thawed sperm quality and fertility of rooster , 2017, Reproduction in domestic animals = Zuchthygiene.

[7]  A. Khaki,et al.  Effects of In Vitro Zinc Sulphate Additive to The Semen Extender on Water Buffalo (Bubalusbubalis) Spermatozoa before and after Freezing , 2014, International journal of fertility & sterility.

[8]  S. R. Salian,et al.  Addition of zinc to human ejaculate prior to cryopreservation prevents freeze-thaw-induced DNA damage and preserves sperm function , 2012, Journal of Assisted Reproduction and Genetics.

[9]  M. Naito,et al.  A Method for Cryopreserving Semen from Yakido Roosters using N-Methylacetamide as a Cryoprotective Agent , 2010 .

[10]  Y. Hsieh,et al.  Seminal malondialdehyde concentration but not glutathione peroxidase activity is negatively correlated with seminal concentration and motility , 2006, International journal of biological sciences.

[11]  J. Long Avian semen cryopreservation: what are the biological challenges? , 2006, Poultry science.

[12]  M. Gavella,et al.  In vitro effect of zinc on oxidative changes in human semen , 1998, Andrologia.

[13]  M. Ardawi,et al.  Effect of marginal or severe dietary zinc deficiency on testicular development and functions of the rat. , 1997, Archives of andrology.

[14]  B. Dresser,et al.  A SIMPLE STAINING METHOD FOR EVALUATING ACROSOMAL STATUS OF CAT SPERMATOZOA , 1991 .

[15]  L. Rothschild,et al.  Counting Live and Dead Bull Spermatozoa , 1953 .

[16]  W. Burrows,et al.  The Collection of Spermatozoa from the Domestic Fowl and Turkey , 1937 .