Improvement in quality of frozen Jersey bull semen following fortification with chloroquine diphosphate and ascorbic acid


409 / 74

Authors

  • MADHUMEET SINGH Professor and Head, Department of Veterinary Gynaecology and Obstetrics, College of Veterinary and Animal Sciences, Himachal Pradesh Agricultural University, Palampur, Himachal Pradesh 176 062 India
  • AKSHAY SHARMA MVSc Scholar, Department of Veterinary Gynaecology and Obstetrics, College of Veterinary and Animal Sciences, Himachal Pradesh Agricultural University, Palampur, Himachal Pradesh 176 062 India

https://doi.org/10.56093/ijans.v88i7.81425

Keywords:

Ascorbic acid, Chloroquine diphosphate, Jersey bulls, Live sperm percentage, Progressive motility

Abstract

The present study was conducted with an objective of studying the role of certain additives e.g. chloroquine diphosphate and ascorbic acid in maintaining the membrane integrity, viability and motility of spermatozoa at various pre- and post-freezing stages of semen of Jersey bulls maintained under sub-temperate climate. Work was conducted at Sperm Station Palampur, Himachal Pradesh, India, on six apparently healthy pure bred Jersey breeding bulls. A total of 36 ejaculates (6 from each bull), were analysed at six different stages of processing namely neat semen evaluation, post-dilution, post-equilibration, post-thaw and after 1 and 2 h incubation post-thaw at 37°C for progressive motility, live dead count, reaction to hypo-osmotic solution and acrosomal integrity, respectively. Evaluation of the semen was done for three groups, i.e. control group (G1), semen fortified with chloroquine diphosphate (G2) and ascorbic acid (G3).The results of the study revealed a significant improvement in progressive motility, live sperm percentage, reaction to hypo-osmotic solution and acrosomal integrity of semen having chloroquine diphosphate (G2) and ascorbic acid (G3) as additives when compared to control group. So, fortification of semen should be done with chloroquine diphosphate and ascorbic acid to improve the quality of semen in future.

Downloads

Download data is not yet available.

References

Al-Khanak K H and Al-Hanak H. 1989. The protective action of tocopherol during cryopreservation of bull semen. Zhivotnov dni Nauki 26: 70–74.

Angasaria H, Pareek P K and Dutt M. 2002. Changes in sperm motility, percent live and acrosome in relation to freezing and thawing in crossbred bull semen. XVIII Annual Convention and National Symposium on Reproductive Technologies for Augmentation of Fertility in Livestock, November 14–16, Izatnagar, India.

Aurich J E, Schonherr U, Hoppe H and Aurich C. 1997. Effect of antioxidants on motility and membrane integrity of chilled stored stallion semen. Theriogenology 48: 185–92. DOI: https://doi.org/10.1016/S0093-691X(97)84066-6

Cecil H C and Baskt M R. 1993. In-vitro lipid peroxidation of turkey spermatozoa. Poultry Science 72: 1370–78. DOI: https://doi.org/10.3382/ps.0721370

Centola G M, Raubertas R F and Mattox J I I. 1992. Cryopreservation of human semen: comparison of cryopreservatives, sources of variability and prediction of postthaw survival. Journal of Andrology 13: 283–88.

Heath E and Gupta R C. 1980. Observations on electron microscopic differentials of bovine spermatozoa. Indian Veterinary Journal 57: 800–05.

Kakar S S and Anand S R. 1984. Acrosomal damage and enzyme leakage during freeze preservation of buffalo spermatozoa. Indian Journal of Experimental Biology 22: 5–10.

Kumar S. 2007. Effect of certain additives in the diluter on postthaw recovery rate of bovine semen. Indian Journal of Veterinary Research 16(1): 29–42.

Lindahl P E. 1966. Sperm agglutinating and antiagglutinating factors in normal follicular fluid from cattle. International Journal of Fertility 11: 297–305.

Nath K C, Ahmad K, Dutta G, Barthakur T and Borgohain B N. 1996. Semen quality and release of certain enzymes during the course of freezing bull spermatozoa. Indian Journal of Animal Reproduction 17: 130–31.

Noakes D E, Parkinson T J and England G C W. 2009. Veterinary Reproduction and Obstetrics. 9th edn.WB Saunders Company Ltd., London.

Norman C and Gombe S. 1975. Stimulatory effect of the lysosomal stabilizer Chloroquine on the respiration and motility of fresh and aged bovine spermatozoa. Journal of Reproduction and Fertility 44: 481–86. DOI: https://doi.org/10.1530/jrf.0.0440481

Rao K N, Rao S, Naidu A S, Naidu K V and Rao M M. 2002. Post thaw evaluation and fertility of bovine semen diluted in Biociphos plus and Tris extenders. Indian Journal of Animal Reproduction 23: 29–31.

Robbins R K, Chandler P T and Saacke R G. 1976. Influences of freeze rate, thaw rate and glycerol level on acrosomal retention and survival of bovine spermatozoa frozen in French straws. Journal of Animal Science 42(1): 145–54. DOI: https://doi.org/10.2527/jas1976.421145x

Sagdeo L R, Chitnis A B, Deshmukh S N and Kaikini A S. 1991. Seasonal variation in relation to freezability of jersey and cross bulls with varying levels of exotic inheritance. Indian Journal of Animal Reproduction 12: 117–21.

Shanmugavel S and Singh S V. 2002. Physical and biochemical constituents of Sahiwal bull semen in relation to their quality. Indian Journal of Animal Sciences 72: 57–58.

Sharma M, Singh M, Kapoor S and Jasial S. 2012. Inter relationship between some routine semen evaluation parameters in Jersey × local hill cattle crossbred bulls. Open Veterinary Journal 2: 26–31. DOI: https://doi.org/10.5455/OVJ.2012.v2.i0.p26

Sidhu S S, Pangawkar G R and Chaudhary R K. 1996. Effect of some additives on the release of enzymes from buffalo spermatozoa during cryopreservation. Indian Veterinary Journal 73: 154–58.

Singh G. 2002. ‘Studies on the effect of additives on membrane integrity and viability of fresh and cryopreserved buffalo bulls spermatozoa. M.V.Sc. Thesis, Punjab Agriculture University, Ludhiana, India.

Singh M M and Nigam J M. 1998. Effect of post-thaw incubation interval to AI on semen quality and conception rate in cattle. Proceedings of Special Celebrating Conference of ICAR, September 14–16, Milan, Italy. pp 600.

Singh M M and Pant H C. 2001. Comparative study on absolute index (motility index) of sperm survival and progressive motility of buffalo and cattle. Indian Veterinary Journal 78: 965–66.

Srivastava S. 2000. ‘Effect of some additives on the freezability of Holstien-Friesisan and Crossbred bulls.’ M.V.Sc. Thesis, IVRI, Izatnagar, Uttar Pradesh.

Srivastava S and Kumar S. 2014. Incorporation of ascorbic acid, caffeine and chloroquine diphosphate in dilutor improves structural and functional status of frozen semen. Open Access Library Journal 1: 1–12. DOI: https://doi.org/10.4236/oalib.1100011

Thakur S. 2003. ‘Studies on some managemental practices responsible for repeat breeding in cattle.’ M.V.Sc. Thesis, CSKHPKV, Palampur, Himachal Pradesh.

Tomar N S, Sharma O P and Singh B P. 1969. Preservation of cattle and buffalo semen at 4ºC to 7ºC. Indian Journal of Dairy Sciences 22: 187–92.

Veeraiah G, Babu R K and Venugopal N K. 1997. The effect of the age of eggs and age of the diluent used on the quality of frozen semen. Indian Journal of Animal Reproduction 18: 65– 66.

Veeraiah G, Venugopal N K and Babu R K. 1999. Effects of various levels of glycerol and egg yolk in freezing of Ongole bull semen. Indian Journal of Animal Reproduction 20: 149– 52.

Verma N K. 1997. ‘Cryopreservation studies of crossbred bull semen with special reference to buffers, membrane stabilizer and seminal enzymes.’M.V.Sc. Thesis, IVRI, Izatnagar, Uttar Pradesh.

Verma A and Kanwar K C. 1998. Human sperm motility and lipid peroxidation in different ascorbic acid concentrations: an in vitro analysis. Andrologia 30: 325–29. DOI: https://doi.org/10.1111/j.1439-0272.1998.tb01178.x

Downloads

Submitted

2018-07-13

Published

2018-07-17

Issue

Section

Articles

How to Cite

SINGH, M., & SHARMA, A. (2018). Improvement in quality of frozen Jersey bull semen following fortification with chloroquine diphosphate and ascorbic acid. The Indian Journal of Animal Sciences, 88(7), 791-794. https://doi.org/10.56093/ijans.v88i7.81425
Citation