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Adenosine triphosphate levels of chinook salmon (Oncorhynchus tshawytscha) eggs following in vitro maintenance and activation/fertilization

Abstract

To further examine the concept of egg quality and the physiology of stored salmonid eggs, we investigated the effects of different oxygen tensions on the adenosine triphosphate (ATP) levels of unfertilized, activated, and fertilized chinook salmon (Oncorhynchus tshawytscha) eggs. The ATP levels of unfertilized chinook salmon eggs were 2.61±0.14 nmol ATP per egg (17.6±0.9 μmol l−1 relative to cell water) and ranged from 1.98 to 3.63 nmol ATP per egg. The ATP content of unfertilized eggs maintained at 10 °C under 100% O2, 21% O2, and 100% N2 remained unaltered throughout a 120 h storage period. Storing eggs under identical conditions at 20 °C (in an effort to speed egg metabolism and ATP turnover) resulted in significant O2-independent decreases in ATP levels. However, ATP levels of unfertilized eggs exposed to 1 mmol l−1 potassium cyanide (a potent inhibitor of oxidative phosphorylation) at 10 °C were significantly decreased after 24 h and continued to decline throughout the 120 h maintenance period to about 30% of time=0 values. Maintenance with exogenous nutrients (5 mmol l−1 acetate plus 5 mmol l−1 pyruvate) over 120 h at 10 °C did not alter the ATP content of unfertilized eggs. Eggs activated by exposing them to 10 °C water for a few minutes showed a rapid decrease in ATP values, regardless of whether the eggs were fertilized or not. Following an initial ∼25% drop after fertilization, the ATP levels remained stable for the remainder (5 d) of the incubation period in eggs maintained in 10 °C water. Therefore, unfertilized chinook salmon egg ATP levels appear to be relatively stable and maintained by a low, cyanide-inhibitable metabolism. The stability of egg ATP levels may be one reason that salmonid eggs can be stored for several days while eggs from other fishes cannot.

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References

  • Bencic, D. C., Krisfalusi, M., Cloud, J. G. and Ingermann, R. L. 1999. ATP levels of chinook salmon (Oncorhynchus tshawytscha) sperm following in vitroexposure to various oxygen tensions. Fish Physiol. Biochem. 20: 389-397.

    Google Scholar 

  • Boulekbache, H., Bastin, J., Andriamihaja, M., Lefebvre, B. and Joly, C. 1989. Ageing of fish oocytes: effects on adenylic nucleotides content, energy charge and viability of carp embryo. Comp. Biochem. Physiol. 93B: 471-476.

    Google Scholar 

  • Brooks, S., Tyler, C. R. and Sumpter, J. P. 1997. Egg quality in fish: what makes a good egg? Rev. Fish Biol. Fish. 7: 387-416.

    Google Scholar 

  • Hayes, F. R., Darcy, D. A. and Sullivan, C. M. 1946. Changes in the inorganic constituents of developing salmon eggs. J. Biol. Chem. 163: 621-631.

    Google Scholar 

  • Jensen, J. O. T. 1988. Combined effects of gas supersaturation and dissolved oxygen levels on steelhead trout (Salmo gairdneri) eggs, larvae, and fry. Aquaculture 68: 131-139.

    Google Scholar 

  • Leung, L. K. P. and Jamieson B. G. M. 1991. Live preservation of fish gametes. In: Fish Evolution and Systematics: Evidence from Spermatozoa. pp. 245-269. Edited by B. G. M. Jamieson. Cambridge University Press, Cambridge.

    Google Scholar 

  • Milman, L. S. and Yurowitsky, Y. G. 1973. Regulation of glycolysis in the early development of fish embryos. Monographs in Develop. Biol. 6. Edited by S. Karger, Basel.

    Google Scholar 

  • Nagler J. J., Parsons J. E. and Cloud J. G. 2000. Single pair mating indicates maternal effects on embryo survival in rainbow trout, Oncorhynchus mykiss. Aquaculture 184: 177-183

    Google Scholar 

  • Renard, Ph., Billard, R. and Christen, R. 1987. Formation of the chorion in carp oocytes. An analysis of the kinetics of its elevation as a function of oocyte ageing, fertilization and the composition of the dilution medium. Aquaculture 62: 153-160.

    Google Scholar 

  • Scott, W. B. and Crossman, E. J. 1975. Freshwater Fishes of Canada. Fisheries Research Board of Canada, Ottawa, Bulletin 184.

    Google Scholar 

  • Srivastava, R. K. and Brown, J. A. 1991. The biochemical characteristics and hatching performance of cultured and wild Atlantic salmon (Salmo salar) eggs. Can. J. Zool. 69: 2436-2441.

    Google Scholar 

  • Stoss, J. 1983. Fish gamete preservation and spermatozoa physiology. In: Fish Physiology. 9B, pp. 305-350. Edited by W. S. Hoar, D. J. Randall and E. M. Donaldson. Academic Press, New York.

    Google Scholar 

  • Terner, C. 1968. Studies of metabolism in embryonic development-I. The oxidative metabolism of unfertilized and fertilized embryonated eggs of the rainbow trout. Comp. Biochem. Physiol. 24: 933-940.

    Google Scholar 

  • Wittenberg, B. A. and Wittenberg, J. B. 1985. Oxygen pressure gradients in isolated cardiac myocytes. J. Biol. Chem. 260: 6548-6554.

    Google Scholar 

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Wendling, N., Bencic, D., Nagler, J. et al. Adenosine triphosphate levels of chinook salmon (Oncorhynchus tshawytscha) eggs following in vitro maintenance and activation/fertilization. Fish Physiology and Biochemistry 22, 217–223 (2000). https://doi.org/10.1023/A:1007870028938

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  • DOI: https://doi.org/10.1023/A:1007870028938

  • air
  • ATP
  • egg
  • fertilization
  • fish
  • hyperoxia
  • hypoxia
  • oxygen