DOI QR코드

DOI QR Code

Seasonal Changes in Concentrations of Proteins and Lipids in Growing Goat Oocytes

  • Sangha, G.K. (Department of Zoology and Fisheries, Punjab Agricultural University) ;
  • Bhatia, H. (Department of Zoology and Fisheries, Punjab Agricultural University) ;
  • Khera, K.S. (Department of Zoology and Fisheries, Punjab Agricultural University)
  • Received : 2005.09.05
  • Accepted : 2005.12.08
  • Published : 2007.01.01

Abstract

Proteins and lipids not only provide a source of energy to the cell, but also play vital roles in modifying the physical properties and function of the biological membranes. In the present study, we investigated the biochemical constituents, viz. proteins and lipids, in growing oocytes of goat antral follicles during summer and winter seasons. Goat genitalia in phosphate buffered saline (pH 7.4) were brought to the laboratory within one hour of slaughter under aseptic conditions at $37^{\circ}C$. Oocytes were aspirated from normal small (<3 mm in diameter) and large (>3 mm) follicles and pooled for biochemical estimations. A significant increase in the amount of protein and lipid was observed with the growth of the oocyte. The amount of protein varied non-significantly with the season, while the amount of lipid varied significantly. The amounts of phospholipid, cholesterol, free fatty acid, and triglyceride increased with the growth of the oocyte, but no significant effect of season in these constituents was observed. Lysolecithin, sphingomyelin, and sterols were the polar lipids identified in both oocytes prepared from small follicles (small oocytes) as well as large follicles (large oocytes). In addition, the small oocytes also contained phosphatidyl serine, while large oocytes contained phosphatidyl glycerol phosphate and phosphatidyl inositol. Among non-polar lipids, triglycerides and long chain alcohols appear only in small oocytes and not in large oocytes. Monoglycerides, 1,2-diglycerides, 1,3-diglycerides and o-dialkyl glycerol ethers, fatty acids, fatty acid methyl esters, and wax esters were identified in both small and large oocytes. Information on biochemical composition of growing oocytes is relevant to oocyte and embryo competence, culture and cryopreservation.

Keywords

References

  1. Ames, B. N. 1966. Methods in Enzymology. 8-11 (Ed. E. F. Newfold and V. Griessburg) Academic Press, New York.
  2. Arav, A., M. Pearl and Y. Zeron. 2000. Does lipid profile explain chilling sensitivity and membrane lipid phase transition of spermatozoa and oocytes? Cryoletters 21(3):179-186.
  3. Buccione, R., A. C. Schroeder and J. J. Epig. 1990. Interaction between somatic cells and germ cells throughout mammalian oogenesis. Biol. Reprod. 43:543-547. https://doi.org/10.1095/biolreprod43.4.543
  4. Canipari, R., A. Pietrolucci and F. Mangia. 1979. Increase of total protein synthesis during mouse oocyte growth. J. Reprod. Fertil. 59:405-413.
  5. Chiamori, N. B. S. and R. J. Henry. 1995. Study of ferric chloride method for determination of total cholesterol and cholesterol esters. Am. J. Clin. Path. 31:305-309.
  6. Cran, D. G. and R. M. Moor. 1990. Programming the oocyte for fertilization. In: Fertilization in Mammals (Ed. B. D. Bavister, J. Cummins and E. R. S. Roldan), Serono Symposia, Norwell MA. pp. 35-37.
  7. Coull, G. B., B. K. Speake, M. E. Staines, P. J. Broadbent and T. G. McEvoy. 1998. Lipid and fatty acid composition of zona intact sheep oocytes. Theriogeneol. 49:179. https://doi.org/10.1016/S0093-691X(98)90532-5
  8. Fair, T., P. Hyttel and T. Greve. 1995. Bovine oocyte diameter in relation to maturational competence and transcriptional activity. Mol. Reg. Dev. 42:437-442. https://doi.org/10.1002/mrd.1080420410
  9. Folch, I., M. Lees and G. H. Sloanestenely. 1957. A simplified method for the isolation and purification of total lipids from animal tissue. J. Biol. Chem. 226:497.
  10. Gall, L., F. le Gall and V. de Smend. 1993. Protein phosphorylation patterns during in vitro maturation of goat oocytes. Mol. Reprod. Dev. 36:500-506. https://doi.org/10.1002/mrd.1080360415
  11. Grealy, M., M. G. Diskin and J. M. Sreeman. 1996. Protein content of cattle oocytes and embryos from the two cell to the elongated blastocyst stage at day 16. J. Reprod. Fertil. 107:229-233. https://doi.org/10.1530/jrf.0.1070229
  12. Guraya, S. S. 2000 Comparative cellular and molecular biology of ovary in mammals: Fundamentals and Applied aspects. Science Publishers, INC, PO Box 699, Enfield, USA.
  13. Homa, S. T., C. Raconsky and R. W. Mc Gouhey. 1986. Lipid analysis of immature pig oocytes. J. Reprod. Fertil. 77:425-434. https://doi.org/10.1530/jrf.0.0770425
  14. Kim, J. Y., M. Kinoshita, M. Ohnishi and Y. Fukui. 2001. Lipid and fatty acid analysis of fresh and frozen thawed immature and in vitro matured oocytes. Reprod. 122:131-138. https://doi.org/10.1530/rep.0.1220131
  15. Lowry, O. H., N. J. Rosebrough, A. L. Farr and R. J. Randall. 1951. Protein measurement with the folin phenol reagent. J. Biol. Chem. 193:265-275.
  16. Lowry, O. H. and I. J. Tinsley. 1976. Rapid calorimetric determination of fatty acids. J. Am. Oil. Chem. Soc. 53:470. https://doi.org/10.1007/BF02636814
  17. Malkar, D. and A. C. Majumdar. 2002. Secretary proteins from goat oocytes matured in culture. Asian-Aust. J. Anim. Sci. 15:340-345. https://doi.org/10.5713/ajas.2002.340
  18. Mc Evoy, T. G., G. D. Coull, P. J. Broadbent, J. S. M. Hutchinson, and B. K. Speake. 2000. Fatty acid composition of lipids in immature cattle, pig and sheep oocytes with intact zona pellucida. J. Rerod. Fertil. 118:163-170. https://doi.org/10.1530/reprod/118.1.163
  19. Nishizuka, Y. 1992. Intracellular signaling by hydrolysis of phospholipids and activation of protein kinase C. Sci. 258:607-614. https://doi.org/10.1126/science.1411571
  20. Randhawa, G. K. 1986. Histochemical and biochemical studies on the follicles and corpora lutea of the rat ovary. Ph.D. Thesis, Punjab Agricultural University Ludhiana, India.
  21. Sangha, G. K. and S. S. Guraya. 1989. Biochemical changes in lipids during follicular growth and corpora lutea formation and regression in rat ovary. Ind. J. Exp. Biol. 27:998-1000.
  22. Schultz, R. M. and P. M. Wassarman. 1977. Biochemical studies of mammalian oogenesis: protein synthesis during oocyte growth and meiotic maturation in the mouse. J. Cell Sci. 24:167-194.
  23. Sharma, R. K. and S. Chowdhary. 1998. Ultrastructure changes in the oocytes of caprine antral follicle. Ind. J. Anim. Sci. 68:332-336.
  24. Sharma, R. K., S. S. Guraya and M. B. Sharma. 2000. Biology of ovarian follicles in the goat: A review. Ind. J. Anim. Sci. 70:369-85.
  25. Stubbs, C. D. and A. D. Smith. 1984. The modifications of mammalian membrane polyunsaturated fatty acid composition in relation to membrane fluidity and function. Biochimica et Biophysica Acta. 779:89-137. https://doi.org/10.1016/0304-4157(84)90005-4
  26. Wilson, S. J., R. S. Marion, J. N. Spain, D. E. Spiers, D. H. Keisler and M. C. Lucy. 1998. Effects of controlled heat stress on ovarian function of dairy cattle. I. Lactating cows. J. Dairy Sci. 81: 2124-2131. https://doi.org/10.3168/jds.S0022-0302(98)75788-1
  27. Wolfenson, D., Z. Roth and R. Meidan. 2000. Impaired reproduction in heat stressed cattle: basic and applied aspects. Anim. Reprod. Sci. 60:535-547. https://doi.org/10.1016/S0378-4320(00)00102-0
  28. Yao, J. K., J. Robert, J. Ryan and P. J. Dyck. 1980. The porcine ovarian follicle.VI. Comparison of fatty acid composition of serum and follicular fluid at different developmental stages. Biol. Reprod. 22:141-147. https://doi.org/10.1095/biolreprod22.2.141
  29. Zeron, Y., A. Ocheretny, O. Kedar, A. Brochov, D. Sklan and A. Arav. 2001. Seasonal changes in bovine fertility: relation to developmental competence of oocytes, membrane properties and fatty acid composition of follicles. Reprod. 121:447-454. https://doi.org/10.1530/rep.0.1210447
  30. Zeron, Y., D. Sklan and A. Arav. 2002. Effect of polyunsaturated fatty acid supplementation on biophysical parameters and chilling sensitivity of ewe oocytes. Mol. Reprod. Dev. 61:271-278. https://doi.org/10.1002/mrd.1156