Effect of fertility associated proteins on lipid peroxidation production in Holstein Friesian semen


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Authors

  • G KRISHNAN Scientist, ICARNational Research Centre on Yak, Dirang. Madras Veterinary College, Chennai, Tamil Nadu 600 007 India
  • A THANGVEL Professor and Head, Madras Veterinary College, Chennai, Tamil Nadu 600 007 India
  • K LOGANATHASAMY Assistant Professor, Department of Veterinary Physiology, Madras Veterinary College, Chennai, Tamil Nadu 600 007 India
  • C VEERAPANDIAN Dean, Veterinary College and Research Institute, Orathnadu
  • P KUMARASAMY Professor and Head, Department of Bioinformatics Centre, Madras Veterinary College, Chennai, Tamil Nadu 600 007 India
  • M KARUNAKARAN Senior Scientist, ICAR-National Dairy Research Institute, ERS, Kalyani, West Bengal

https://doi.org/10.56093/ijans.v85i11.53060

Keywords:

Bull, Fertility associated proteins, Lipid peroxidation, Semen, Sperm viability

Abstract

Present study was designed to evaluate effects of fertility associated proteins on sperm motility, viability and level of lipid peroxidation (LPO) in semen. Holstein Friesian breeding bulls (17) were screened for fertility associated proteins (24, 28–30 and 55 kDa proteins), and categorized into 8 groups based on presence/absence in the seminal plasma and sperm membrane. Level of LPO compound malondialdehyde (MDA) was assessed in fresh and frozenthawed semen using thiobarbituric acid method. Fresh semen of bulls positive for fertility associated proteins had lower MDA (0.433±0.03 μmol/ml) than bulls negative for fertility associated proteins (0.740±0.05 μmol/ml). Level of MDA increased in frozen-thawed sperm by 1.5 fold as that of fresh semen among bulls positive for fertility associated proteins and 2 fold in negative bulls. MDA level increased by 27% in all the frozen-thawed semen incubated at 37°C for 180 min, however it was lower in bulls with fertility associated proteins (2.380±0.14 μmol/ ml) than negative bulls. Fresh semen with fertility associated proteins had higher number of motile sperm with progressive motility than negative bulls. Further, bulls with fertility associated proteins were able to sustain higher number of viable sperms with progressive motility than negative group at the end of 180 min of incubation. The results concluded that the fertility associated proteins were capable to sustain sperm viability and motility by limiting LPO production in fresh and frozen-thawed semen.

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References

Asadpour R, Alavi-Shoushtari S M, Asri Rezaii S, Khan M H and Ansari K M. 2007. SDS-polyacrylamide gel electrophoresis of buffalo bulls seminal plasma proteins and their relation with semen freezability. Animal Reproduction Science 102: 308–13. DOI: https://doi.org/10.1016/j.anireprosci.2007.03.003

Asadpour R, Jafari R and Tayefi-Nasrabadi H. 2011. Effect of various levels of catalase antioxidant in semen extenders on lipid peroxidation and semen quality after the freeze-thawing bull semen. Veterinary Research Forum 2 (4): 218–21.

Ashrafi I, Kohram H and Tayefi-Nasrabadi H. 2013. Antioxidant effects of bovine serum albumin on kinetics, microscopic and oxidative characters of cryopreserved bull spermatozoa. Spanish Journal of Agricultural Research 11 (3): 695–701. DOI: https://doi.org/10.5424/sjar/2013113-3870

Bansal A K and Bilaspuri G S. 2011. Impacts of oxidative stress and antioxidants on semen functions. Veterinary Medicine International 37: 1–7. DOI: https://doi.org/10.4061/2011/686137

Bustamante-Filho I C, Salton G D, Munari F M, Schneider M R, Mattos R C, Laurino J P, Cirne-Lima E O and Jobim M I M. 2014. Recombinant expression and purification of the bovine acidic seminal fluid protein. Animal Reproduction 11 (2): 96– 103.

Jobim M I M, Oberst E R, Salbego C G, Souza D O, Wald V B, Tramontina F and Mattos R C. 2004. Two-dimensional polyacrylamide gel electrophoresis of bovine seminal plasma proteins and their relation with semen freezability. Theriogenology 61: 255–66. DOI: https://doi.org/10.1016/S0093-691X(03)00230-9

Karunakaran M, Devanathan T G, Kulasekar K, Sridevi P, Jawahar T P, Loganathsamy K, Dhali A and Selvaraju S. 2012. Effect of heparin binding protein and hydrogen peroxide on lipid peroxidation status of bovine sperm cells. Indian Journal of Animal Sciences 82 (9): 976–78.

Kutty M V H, Remya V, Shyma V H, Radhika S, Shende A M and Bhure S K. 2014. An overview on binder of sperm proteins of cattle. International Journal of Livestock Research 4 (4): 1–11. DOI: https://doi.org/10.5455/ijlr.20140629034437

Laemmli V K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 660– 85. DOI: https://doi.org/10.1038/227680a0

Manaskova P, Liberda J V, Ticha M and Jonakova V. 2002. Isolation of non-heparin-binding and heparin-binding proteins of boar prostate. Journal of Chromatography 770: 137– 43. DOI: https://doi.org/10.1016/S0378-4347(01)00480-7

Moura A A, Koc H, Chapman D A and Killian G J. 2006. Identification of proteins in the accessory sex gland fluid associated with fertility indexes of dairy bulls: a proteomic approach. Journal of Andrology 27 (2): 201–11. DOI: https://doi.org/10.2164/jandrol.05089

Parisi A M, Thompson S K, Kaya A and Memili E. 2014. Molecular, cellular and physiological determinants of bull fertility. Turkish Journal of Veterinary and Animal Sciences 38: 637–42. DOI: https://doi.org/10.3906/vet-1404-76

Sarsaifi K, Vejayan J, Haron A W, Yusoff R, Hani H, Rasoli M, Omar M A and Othman AM. 2015. Protein profile and functionality of spermatozoa from two semen collection methods in Bali bulls. Livestock Science 172: 96–105. DOI: https://doi.org/10.1016/j.livsci.2014.12.004

Singh M, Ghosh S K, Prasad J K, Kumar A, Tripathi R P, Bhure S K and Srivastava N. 2014. Seminal PDC–109 protein vis-avis cholesterol content and freezability of buffalo spermatozoa. Animal Reproduction Science 144 (1–2): 22–29. DOI: https://doi.org/10.1016/j.anireprosci.2013.10.016

Suleiman S A, Ali M E, Zaki M S, Malik E M E A and Nast M A. 1996. Lipid peroxidation and human sperm motility protective role of vitamin E. Journal of Andrology 17 (5): 530–37.

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2015-11-03

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2015-11-03

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How to Cite

KRISHNAN, G., THANGVEL, A., LOGANATHASAMY, K., VEERAPANDIAN, C., KUMARASAMY, P., & KARUNAKARAN, M. (2015). Effect of fertility associated proteins on lipid peroxidation production in Holstein Friesian semen. The Indian Journal of Animal Sciences, 85(11), 1176–1180. https://doi.org/10.56093/ijans.v85i11.53060
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