Skip to main content

Advertisement

Log in

The antioxidant system of sterlet seminal fluid in testes and Wolffian ducts

  • Published:
Fish Physiology and Biochemistry Aims and scope Submit manuscript

Abstract

Oxidative stress is a possible source of spermatozoa function deterioration. Seminal fluid (SF) protects spermatozoa against reactive oxygen species (ROS) attack during development in testes and transit through the reproductive tract. Spermatozoa curvilinear velocity and percent of motile cells as well as changes in thiobarbituric acid-reactive substance (TBARS) content, superoxide dismutase, and catalase activity, and uric acid concentration in SF were evaluated in sterlet sperm collected from testes 24 h after hormone induction of spermiation and from Wolffian ducts at 12, 24, 36, and 60 h after hormone injection (HI). While testicular spermatozoa motility was not initiated in activating medium, Wolffian duct sperm showed low motility at 12 h, significant increase at 24 and 36 h, and decrease at 60 h. Testicular SF was characterized by the highest level of TBARS and activity of studied enzymes compared with SF from Wolffian duct sperm at 24 h post-HI. In fluid from Wolffian duct sperm, a significant increase in TBARS content was shown at 36–60 h post-HI. In contrast to testicular SF, in SF from Wolffian duct sperm, this increase was not counterbalanced by changes in the studied variables of antioxidant system. This may be the source of the observed decrease in spermatozoa motility parameters 60 h post-HI. The results may confirm a dual role of ROS in fish sperm physiology. The data with respect to decrease in sturgeon spermatozoa motility parameters at 60 h post-HI should be taken into account in artificial sturgeon propagation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Explore related subjects

Discover the latest articles and news from researchers in related subjects, suggested using machine learning.

References

  • Agarwal A, Saleh RA (2002) Role of oxidants in male infertility: rationale, significance, and treatment. Urol Clin N Am 29:817–827

    Article  Google Scholar 

  • Aitken RJ, Baker MA, Sawyer D (2003) Oxidative stress in the male germ line and its role in the aetiology of male infertility and genetic disease. Reprod Biomed Online 7:65–70

    Article  CAS  PubMed  Google Scholar 

  • Aitken RJ, Jones KT, Robertson SA (2012) Reactive oxygen species and sperm function—in sickness and in health. J Androl 33:1096–1106

    Article  CAS  PubMed  Google Scholar 

  • Asakawa T, Matsushita S (1980) Coloring conditions of thiobarbituric acid test for detecting lipid hydroperoxides. Lipids 15:137–140

    Article  CAS  Google Scholar 

  • Baumber J, Ball BA (2005) Determination of glutathione peroxidase and superoxide dismutase-like activities in equine spermatozoa, seminal plasma, and reproductive tissues. Am J Vet Res 66:1415–1419

    Article  CAS  PubMed  Google Scholar 

  • Chabory E, Damon C, Lenoir A, Henry-Berger J, Vernet P, Cadet R, Saez F, Drevet JR (2010) Mammalian glutathione peroxidases control acquisition and maintenance of spermatozoa integrity. J Anim Sci 88:1321–1331

    Article  CAS  PubMed  Google Scholar 

  • Ciereszko A, Dabrowski K, Kucharczyk D, Dobosz S, Goryczko K, Glogowski J (1999) The presence of uric acid, an antioxidantive substance, in fish seminal plasma. Fish Physiol Biochem 21:313–315

    Article  CAS  Google Scholar 

  • de Lamirande E, Leclerc P, Gagnon C (1997) Capacitation as a regulatory event that primes spermatozoa for the acrosome reaction and fertilization. Mol Hum Reprod 3:175–194

    Article  PubMed  Google Scholar 

  • Duncan PH, Gochman N, Cooper T, Smith E, Bayse D (1982) A candidate reference method for uric acid in serum. I. Optimization and evaluation. Clin Chem 28:284–290

    CAS  PubMed  Google Scholar 

  • Dzyuba B, Boryshpolets S, Shaliutina A, Rodina M, Yamaner G, Gela D, Dzyuba V, Linhart O (2012) Spermatozoa motility, cryoresistance, and fertilizing ability in sterlet Acipenser ruthenus during sequential stripping. Aquaculture 356–357:272–278

    Article  Google Scholar 

  • Dzyuba B, Cosson J, Boryshpolets S, Bondarenko O, Dzyuba V, Prokopchuk G, Gazo I, Rodina M, Linhart O (2014) In vitro sperm maturation in sterlet, Acipencer ruthenus. Reprod Biol 14:160–163

    Article  PubMed  Google Scholar 

  • Fisher HM, Aitken RJ (1997) Comparative analysis of the ability of precursor germ cells and epididymal spermatozoa to generate reactive oxygen metabolites. J Exp Zool 277:390–400

    Article  CAS  PubMed  Google Scholar 

  • Flajshans M, Cosson J, Rodina M, Linhart O (2004) The application of image cytometry to viability assessment in dual fluorescence-stained fish spermatozoa. Cell Biol Int 28:955–959

    Article  CAS  PubMed  Google Scholar 

  • Ford WCL (2004) Regulation of sperm function by reactive oxygen species. Hum Reprod Update 10:387–399

    Article  CAS  PubMed  Google Scholar 

  • Hagedorn M, McCarthy M, Carter VL, Meyers SA (2012) Oxidative stress in zebrafish (Danio rerio) sperm. PLoS One 7:e39397

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Hoar WS (1969) Reproduction. In: Hoar WS, Randall DJ (eds) Fish physiology, vol 3, 1st edn. Academic Press, New York and London, pp 1–72

    Google Scholar 

  • Kasimanickam R, Kasimanickam V, Thatcher CD, Nebel RL, Cassell BG (2007) Relationships among lipid peroxidation, glutathione peroxidase, superoxide dismutase, sperm parameters, and competitive index in dairy bulls. Theriogenology 67:1004–1012

    Article  CAS  PubMed  Google Scholar 

  • Lahnsteiner F, Mansour N (2010) A comparative study on antioxidant systems in semen of species of the Percidae, Salmonidae, Cyprinidae, and Lotidae for improving semen storage techniques. Aquaculture 307:130–140

    Article  CAS  Google Scholar 

  • Lahnsteiner F, Mansour N, Plaetzer K (2010) Antioxidant systems of brown trout (Salmo trutta f. fario) semen. Anim Reprod Sci 119:314–321

    Article  CAS  PubMed  Google Scholar 

  • Marengo SR (2008) Maturing the sperm: unique mechanisms for modifying integral proteins in the sperm plasma membrane. Anim Reprod Sci 105:52–63

    Article  CAS  PubMed  Google Scholar 

  • Marklund S, Marklund G (1974) Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 47:469–474

    Article  CAS  PubMed  Google Scholar 

  • Marklund S, Nordensson I, Back O (1981) Normal CuZn superoxide dismutase, Mn superoxide dismutase, catalase and glutathione peroxidase in Werner’s syndrome. J Gerontol 36:405–409

    Article  CAS  PubMed  Google Scholar 

  • Miura T, Miura C (2001) Japanese eel: a model for analysis of spermatogenesis. Zool Sci 18:1055–1563

    Article  Google Scholar 

  • Miura T, Kasugai T, Nagahama Y, Yamauchi K (1995) Acquisition of potential for sperm motility in vitro in Japanese eel Anguilla japonica. Fish Sci 61:533–534

    CAS  Google Scholar 

  • Morisawa S, Morisawa M (1986) Acquisition of potential for sperm motility in rainbow trout and chum salmon. J Exp Biol 126:89–96

    CAS  PubMed  Google Scholar 

  • Morisawa S, Morisawa M (1988) Induction of potential for sperm motility by bicarbonate and pH in rainbow trout and chum salmon. J Exp Biol 136:13–22

    CAS  PubMed  Google Scholar 

  • Ohta H, Ikeda K, Izawa T (1997) Increases in concentrations of potassium and bicarbonate ions promote acquisition of motility in vitro by Japanese eel spermatozoa. J Exp Zool 277:171–180

    Article  CAS  Google Scholar 

  • Potts RJ, Notarianni LJ, Jefferies TM (2000) Seminal plasma reduces exogenous oxidative damage to human sperm, determined by the measurement of DNA strand breaks and lipid peroxidation. Mutat Res 447:249–256

    Article  CAS  PubMed  Google Scholar 

  • Rhemrev JP, van Overveld FW, Haenen GR, Teerlink T, Bast A, Vermeiden JP (2000) Quantification of the nonenzymatic fast and slow TRAP in a postaddition assay in human seminal plasma and the antioxidant contributions of various seminal compounds. J Androl 21:913–920

    CAS  PubMed  Google Scholar 

  • Schulz RW, de Franca LR, Lareyre JJ, LeGac F, Chiarini-Garcia H, Nobrega RH, Miura T (2010) Spermatogenesis in fish. Gen Comp Endocrinol 165:390–411

    Article  CAS  PubMed  Google Scholar 

  • Shaliutina A, Hulak M, Gazo I, Linhartova P, Linhart O (2013) Effect of short-term storage on quality parameters, DNA integrity, and oxidative stress in Russian (Acipenser gueldenstaedtii) and Siberian (Acipenser baerii) sturgeon sperm. Anim Reprod Sci 139:127–135

    Article  CAS  PubMed  Google Scholar 

  • Shiva M, Gautam AK, Verma Y, Shivgotra V, Doshi H, Kumar S (2011) Association between sperm quality, oxidative stress, and seminal antioxidant activity. Clin Biochem 44:319–324

    Article  CAS  PubMed  Google Scholar 

  • Sikka SC, Rajasekaran M, Hellstrom WJG (1995) Role of oxidative stress and antioxidants in male infertility. J Androl 16:464–468

    CAS  PubMed  Google Scholar 

  • Sostaric E, Aalberts M, Gadella BM, Stout TAE (2008) The roles of the epididymis and prostasomes in the attainment of fertilizing capacity by stallion sperm. Anim Reprod Sci 107:237–248

    Article  CAS  PubMed  Google Scholar 

  • Tavilani H, Goodarzi MT, Vaisi-raygani A, Salimi S, Hassanzadeh T (2008) Activity of antioxidant enzymes in seminal plasma and their relationship with lipid peroxidation of spermatozoa. Int Braz J Urol 34:485–491

    Article  PubMed  Google Scholar 

  • Turner TT, Lysiak JJ (2008) Oxidative stress: a common factor in testicular dysfunction. J Androl 29:488–498

    Article  CAS  PubMed  Google Scholar 

  • Vizziano D, Fostier A, Loir M, Le Gac F (2008) Testis development, its hormonal regulation and spermiation induction in teleost fish. In: Alavi SMH, Cosson JJ, Coward K, Rafiee G (eds) Fish spermatology, 1st edn. Alpha Science International Ltd, Oxford, pp 103–139

    Google Scholar 

Download references

Acknowledgments

The authors acknowledge financial support from projects: CENAKVA CZ.1.05/2.1.00/01.0024, Strengthening of excellence scientific teams in USB FFPW CZ.1.07/2.3.00/20.0024, GAJU 114/2013/Z, GACR P502/11/0090, and 502/12/1973. The results of the project LO1205 were obtained with financial support from the MEYS of the CR under the NPU I program. The Lucidus Consultancy, UK, is gratefully acknowledged for the English correction and suggestions.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Viktoriya Dzyuba.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Dzyuba, V., Dzyuba, B., Cosson, J. et al. The antioxidant system of sterlet seminal fluid in testes and Wolffian ducts. Fish Physiol Biochem 40, 1731–1739 (2014). https://doi.org/10.1007/s10695-014-9963-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10695-014-9963-2

Keywords

Profiles

  1. Sergii Boryshpolets