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ISSN 2522-9028 (Print)
ISSN 2522-9036 (Online)
DOI: https://doi.org/10.15407/fz

Fiziologichnyi Zhurnal

is a scientific journal issued by the

Bogomoletz Institute of Physiology
National Academy of Sciences of Ukraine

Editor-in-chief: V.F. Sagach

The journal was founded in 1955 as
1955 – 1977 "Fiziolohichnyi zhurnal" (ISSN 0015 – 3311)
1978 – 1993 "Fiziologicheskii zhurnal" (ISSN 0201 – 8489)
1994 – 2016 "Fiziolohichnyi zhurnal" (ISSN 0201 – 8489)
2017 – "Fiziolohichnyi zhurnal" (ISSN 2522-9028)

Fiziol. Zh. 2016; 62(2): 47-56


INDUCTION OF OXIDATIVE AND NITROSATIVE STRESS IN BOYS IN ADAPTING TO PHYSICAL STRESS DURING TRAINING AND COMPETITIVE PERIODS

N.V. Bogdanovskaya, A.V. Kotsuruba, A.V. Golubenko

    O.O.Bogomoletz Institute of Physiology of the National Academy of Sciences of Ukraine, Kyiv.
DOI: https://doi.org/10.15407/fz62.02.047


Abstract

We studied the features of development of oxidative and nitrosative stress in otherwise healthy individuals under the influence of prolonged exercise of high volume and intensity. It is shown that young men who systematically performed muscular work have a high content of markers of different ways of generation of superoxide radical, a reactive oxygen species for products of lipid peroxidation and markers of nitrosative stress. The increase in the degree of adverse effects on the body intensive training and competitive loads is accompanied by pronounced adaptive changes in the hierarchy of oxidizing constitutive de novo synthesis of nitric oxide, as well as its nonoxide reutilization synthesis (in 3 times higher). Disadaptation of the organism of boys at the end of the competition period is reflected in growing levels of generation of ROS (superoxide radical: 3,5 times higher, hydrogen peroxide: 2,5 times higher). The products of purine nucleotides degradation were 2 times higher, and the increase in the content of the nitrate anion was 2,5 times higher.

Keywords: induction; oxidative stress; nitrosative stress; adaptation; physical activity.

References

  1. Martinovich GG, Cherenkevich SN. Oxidation-reduction processes in cells: Monograph. Mn.: BSU, 2008. 159 P. [Russian]. PubMedCentral
  2.  
  3. Davies KJ, Quintanilha AT, Brooks GA, Packer L. Free radicals and tissue damage produced by exercise. Biochem Biophys Res Commun. 1982; 107:1198-05. CrossRef  
  4. Andras Perl Oxidative stress in the pathology and treatment of systemic lupus erythematosus. Nat Rev Rheumatol. 2013; 9 (11):674-86. CrossRef PubMed PubMedCentral
  5.  
  6. Thomas J. Grahame and Richard B. Schlesinger Grahame Oxidative stress-induced telomeric erosion as a mechanism underlying airborne particulate matter-related cardiovascular disease. Part Fibre Toxicol. 2012; 9; 9-21.
  7.  
  8. Dario Pitocco, Manfredi Tesauro, Rizzi Alessandro, Giovanni Ghirlanda, and Carmine Cardillo Oxidative Stress in Diabetes: Implications for Vascular and Other Complications. Int J Mol Sci. 2013, 14(11):21525–50. CrossRef PubMed PubMedCentral
  9.  
  10. Dvorschenko KO. The effect of ionizing radiation and hydrogen peroxide on the performance of oxide - antioxidant balance and energy metabolism in thymocytes and hepatocytes in vitro. Kiev national University of Taras Shevchenko. 2004; 20 [Ukrainian].
  11.  
  12. Gomez-Cabrera M, Domenech E, Vi-a J. Moderate exercise is an antioxidant: upregulation of antioxidant genes by training. Free Radical Biology and Medicine. 2008;44 (2): 126-31. CrossRef PubMed
  13.  
  14. Gavrilov VB., Gavrilova AG. The Measurement of diene conjugates in plasma blood by UV absorption of heptane and isopropanol extracts. The lab. case. 1988; 2:60-3.
  15.  
  16. Biochemical research methods in the clinic. Guide. Medicine. 1969:652.
  17.  
  18. McCord J., Fridovich I.A. A quantitative test for superoxide radicals produced in biological systems. Biochem. J. 1982; 203(3): 551–8. CrossRef  
  19. Conte D., Narindrasorasa KS., Sarkar B. In vivo and in vitro iron replaced zinc finger generates free radicals and causes DNA damage. Eur. J. Biochem. 1996; 271(9):5125–30.
  20.  
  21. Huwiler M., Kohler H.Pseudo-catalic degradation of hydrogen peroxide in lactoperoxidase iodide system. Eur. journal Biochemistry. 1984; 1:69-4. CrossRef  
  22. Uchiyama M., Mihara M. Determination of malonaldehyde precursor in tissues by thiobarbituric acid test Anal. Biochem. 1978; 86 (1):271-8. CrossRef  
  23. Salter M., Knowles RG., Moncada S. Widespread tissue distribution, species and changes in activity of Ca2+- dependent and Ca2+-independent nitric oxide syntases. FEBS Lett. 1991;291 (1):145-9. CrossRef  
  24. So Yeon Chin, kailash n. Pandey, Shang-Jin Shi, Hiroyuki Kobori, Carol Moreno, And L. Gabriel Navar. Increased activity and expression of Ca2+-dependent NOS in renal cortex of ANG II-infused hypertensive rats. Amer. J. Physiol. 1999;277 (5 Pt. 2):797-4.
  25.  
  26. Svenson AA. Rapid and Sensitive Spectropholometric Method for Determination of Hydrogen Sulfide with 2,2'-dipyridyl disulfide. Anal Biochem. 1980;107:51-5. CrossRef  
  27. Jsukahara H. Effect of NOS inhibitions on bone methabolizm in growing rats. Am J. Physiol. 1996; (270)5:840-5.
  28.  
  29. Alikulov ZA., Lviv NP., Kretovich VL. Nitrate and nitrite is activity of milk. BioChem. 1980;45(9):1714-8 [Russian].
  30.  
  31. Shugaley VS, Kozina AS. The content of urea and arginase activity in the organs of rats during acclimatization to cold // Fiziol Zh. USSR. 1977; 8:1199-2.
  32.  
  33. Garganta CL, Bond JS. Assay and kinetics ot'arginase Anal Biochem. 1982;126 (l):131-8.
  34.  
  35. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin reagent. J. Biol. Chem. 1951;193:265–75. PubMed
  36.  
  37. Gutteredge JM. Lipid peroxidation and antioxidants as biomarkers of tissue damage. Clin Chemistry. 995;41:1819-28.
  38.  
  39. Bogdanovska NV, Kotsuruba AV, Malikov MV. Features of metabolism of arginine and nitric oxide synthesis in young men during adaptation to physical stress during training and competitive periods Fiziol Zh. 2011;57, 1:45-54 [Ukrainian]. CrossRef  
  40. Sojitra B, Bulani Y, Putcha UK, Kanwal A, Gupta P, Kuncha M, Banerjee SK. Nitric oxide synthase inhibition abrogates hydrogen sulfide-induced cardioprotection in mice. Mol Cell Biochem. 2012;360:61-9. CrossRef PubMed
  41.  
  42. Green D, Maiorana A, Driscoll G, Taylor R. Effect of exercise training on endothelium-derived nitric oxide function in humans J. Physiol. 2004; 561(1):1-25. CrossRef PubMed PubMedCentral
  43.  
  44. Rakhmanov RS, Troshin VV, Blinova TV, Strakhova LA. Correction of immunodeficiency States and antioxidative status during strenuous exercises products with a high content of biologically active substances. Med Almanac. 2012;3:156-8 [Russian].

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