Effect of Drinking Ration with Reduced Deuterium Content on Brain Tissue Prooxidant-Antioxidant Balance in Rats with Acute Hypoxia Model
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Keywords

DDW
hypoxia
brain
catalase
SOD

How to Cite

Alexander A. Kravtsov, Stanislav V. Kozin, Ekaterina R. Vasilevskaya, Anna A. Elkina, Lilia V. Fedulova, Konstantin A. Popov, Vadim V. Malyshko, Arkady V. Moiseev, DenisI.Shashkov , & Mikhail G. Baryshev. (2018). Effect of Drinking Ration with Reduced Deuterium Content on Brain Tissue Prooxidant-Antioxidant Balance in Rats with Acute Hypoxia Model . Journal of Pharmacy and Nutrition Sciences, 8(2), 42–51. https://doi.org/10.6000/1927-5951.2018.08.02.3

Abstract

The aim was to investigate prooxidant-antioxidant system in the blood and brain homogenates functional activity in rats with acute hypoxia model with different deuterium/protium (D/H) ratios in drinking diet. Studies have shown that consuming DDW (–665 ‰) within 8 weeks lead to deuterium concentration decrease in blood plasma at 317 ‰ and brain at 209 ‰ of rats, in comparison to control group, consuming natural water. DDW consumption before hypoxia modeling in rats improves antioxidant defense enzymes (catalase, superoxide dismutase, glutathione peroxidase and glutathione reductase) activity in the blood, increasing its antioxidant potential by 20 %, while free radical oxidation intensity in plasma and biomolecules peroxide modification rate in erythrocytes. Also, in brain tissues consuming DDW, there were no abnormalities in catalase, superoxide dismutase activity, and it was noted increase (by 71 %) in reduced thiol-containing compounds concentration, which reduces nerve hypoxi? cell damage risk. Neuroprotective effect presence is confirmed by higher (by 32 %) antioxidant activity markers of lyophilized brain tissues, and by free radical oxidation lower intensity (by 13 %) and biomolecules oxidative modification rate (by 16 %) in these lyophilized tissues. Thus, the advisability of using DDW neuroprotective effects in cerebral circulation disturbance in experimental and clinical practice.

https://doi.org/10.6000/1927-5951.2018.08.02.3
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References

Mehri S, Dadesh Q, Tabeshpour J, et al. Evaluation of the Neuroprotective Effect of Silymarin on Acrylamide-Induced Neurotoxicity. Jundishapur J Nat Pharm Prod 2016; 11(4): e37644.

Vodop’yanova OA, Moiseeva IYa, Rodina OP et al. The influence of cytoflavin and cardioxipin on the indices of lipid peroxidation and antioxidant protection in the blood of rat with dyslipidemia. Experimental and Clinical Pharmacology 2014; 77(6): 27-29.

De Wind LJ, Willems J, Roemen TH et al. Ischemic: reperfused isolated working mouse heart: membrane damage and type II A phospholipase A. Am. J. Physiol. Heart Cire Physiol 2001; 280(6): 2572-2580.

Ziemka-Nalecz M, Zalewska T. Neuroprotective effects of histone deacetylase inhibitors in brain ischemia. Acta Neurobiologiae Experimentalis 2014; 74(4): 383-395.

Shakhmardanova SA, Shakhmardanov AZ. Antihypoxia activiti of the metal complexes of zinc, cobalt and iron and their effect on the behavior of animals. Bulletin of the VSU. Series: Chemistry. Biology. Pharmacy 2014; 4: 142-146.

Voronina TA. Mexidol: main neuropsychotropic effects and mechanisms of action. Pharmatec 2009; 6: 28-31.

Kikuchi K, Tanaka E, Murai Yo et al. Clinical Trials in Acute Ischemic Stroke. CNS Drugs 2014; 28(10): 929-938. https://doi.org/10.1007/s40263-014-0199-6

Shurygina LV, Kravtsov AA, Zlishcheva EI et al. Neuroprotective effect of potassium comenate against glutamate toxicity on the model of cultured rat cerebellar neurons. Bulletin of Experimental Biology and Medicine 2014; 158(1): 49-52. https://doi.org/10.1007/s10517-014-2689-4

Stocchetti N, Taccone FS, Citerio G et al. Neuroprotection in acute brain injury: an up-to-date review. Critical Care 2015. https://doi.org/10.1186/s13054-015-0887-8

Tuttolomondo A, Pecoraro R, Arnao V et al. Developing drug strategies for the neuroprotective treatment of acute ischemic stroke. Expert. Rev. Neurother 2015; 15(11): 1271-1284. https://doi.org/10.1586/14737175.2015.1101345

Shurygina LV, Zlishcheva EI, Androsova TV et al. Effect of potassium komenate on the functional state of the CNS of animals under normal and hypoxic conditions with hypercapnia. Bulletin of Experimental Biology and Medicine 2016; 161(5): 585-589. https://doi.org/10.1007/s10517-016-3476-1

Amara Y, Meddah B, Bonacorsi I et al. Phytochemicals, Antioxidant and Antiproliferative Properties of Rosmarinus officinalis L on U937 and CaCo-2 Cells. Iranian Journal of Pharmaceutical Research 2017; 16(1): 315-327.

Tymianski M. Novel Approaches to Neuroprotection Trials in Acute Ischemic Stroke. Stroke 2013; 44: 2942-2950. https://doi.org/10.1161/STROKEAHA.113.000731

Shurygina LV, Zlishcheva EI, Khablyuk VV et al. Comparative Analysis of Antioxidant Properties of Comenic Acid and Potassium Comenate in Modeled Immobilization Stress. Bulletin of Experimental Biology and Medicine 2015; 159(4): 466-468. https://doi.org/10.1007/s10517-015-2993-7

Esmaeelpanah E, Rahmatkhah A, Poormahmood N et al. Protective Effect of Green Tea Aqueous Extract on Acrylamide Induced Neurotoxicity. Jundishapur J Nat Pharm Prod 2015; 10(2): e18406.

Sharifzadeh M, Ranjbar A, Hosseini A et al. The Effect of Green Tea Extract on Oxidative Stress and Spatial Learning in Streptozotocin-diabetic Rats. Iranian Journal of Pharmaceutical Research 2017; 16(1): 201-209.

Minnerup J, Sutherland BA, Buchan AM et al. Neuroprotection for Stroke: Current Status and Future Perspectives. Int J Mol Sci 2012; 13: 11753-11772. https://doi.org/10.3390/ijms130911753

Stocchetti N, Taccone FS, Citerio G et al. Neuroprotection in acute brain injury: an up-to-date review. Critical Care 2015. https://doi.org/10.1186/s13054-015-0887-8

Tuttolomondo A, Pecoraro R, Arnao V et al. Developing drug strategies for the neuroprotective treatment of acute ischemic stroke. Expert. Rev. Neurother 2015; 15(11): 1271-1284. https://doi.org/10.1586/14737175.2015.1101345

Strekalova T, Evans M, Chernopiatko A et al. Deuterium content of water increases depression susceptibility: The potential role of a serotonin-related mechanism. Behavioral Brain Research 2015; 277: 237-244. https://doi.org/10.1016/j.bbr.2014.07.039

Mladin C, Ciobica A, Lefter R et al. Deuterium depletion induces anxiolytic-like effects in rats. Archives of Biological Science 2014; 66(2): 947-953. https://doi.org/10.2298/ABS1402947M

Fernandes de Lima VM, Hanke W. Modulation of CNS excitability by water movement. The D2O effects on the non-linear neuron-glial dynamics. Journal of Biophysical Chemistry 2011; 2(3): 353-360. https://doi.org/10.4236/jbpc.2011.23040

Dzhimak SS, Basov AA, Fedulova LV et al. Correction of metabolic processes in rats during chronic endotoxicosis using isotope (D/H) exchange reactions. Biology Bulletin 2015. https://doi.org/10.1134/S1062359015050064

Bild W, Stefanescu I, Haulica I et al. Research concerning the radioprotective and immunostimulating effects of deuterium-depleted water. Rom J Physiol 1999; 36(3-4): 205-218.

Rakov DV, Erofeeva LM, Grigorenko DE. Influence of water with a low content of heavy stable hydrogen isotope deuterium and oxygen 18O on the development of radiation damage in gamma irradiation in low dose. Radiation Biology. Radioecology 2006; 46(4): 475-479.

Rakov DV. Alleviation of gamma-radiation damage by water with reduced deuterium and 18? content. Aerospace and Environmental Medicine 2007; 41(3): 36-39.

Thiel A, Cechetto DF, Heiss WD et al. Amyloid Burden, Neuroinflammation, and Links to Cognitive Decline After Ischemic Stroke. Stroke. (2014) 45: 2825-2829.

Dzhimak SS, Basov AA, Baryshev MG. Content of deuterium in biological fluids and organs: influence of deuterium depleted water on D/H gradient and the process of adaptation. Doklady Biochemistry and Biophysics 2015; 465: 370-373. https://doi.org/10.1134/S1607672915060071

Dzhimak SS, Barishev MG, Basov AA et al. Influence of deuterium depleted water on freeze dried tissue isotopic composition and morphofunctional body performance in rats of different generations. Biophysics 2014; 59(4): 614-619. https://doi.org/10.1134/S0006350914040101

Fedulova LV, Dzhimak SS, Kotenkova EA et al. Influence of deuterium depleted water on rat physiology: reproductive function, forming and posterity development. Journal of Pharmacy and Nutrition Sciences 2016; 6(2): 55-60. https://doi.org/10.6000/1927-5951.2016.06.02.3

Mladin C, Ciobica A, Lefter R et al. Deuterium-depleted water has stimulating effects on long-term memory in rats. Neurosci. Lett 2014; 7(583): 154-158.

Guide for the Care and Use of Laboratory Animals: Eighth Edition. DC: The National Academies Press, Washington 2011: 248.

Dzhimak SS, Basov AA, Kopytov GF et al. Application of NMR spectroscopy to the determination of low concentrations of nonradioactive isotopes in liquid media. Russian Physics Journal 2015; 58(7): 923-929. https://doi.org/10.1007/s11182-015-0591-9

Rothman LS, Jacquemart D, Barbe A et al. The HITRAN 2004 molecular spectroscopic database. J. Quant. Spectrosc. Radiat. Transfer 2005; 96: 139-204.

Lisicin AB, Barishev MG, Basov AA et al. Influence of deuterium depleted water on the organism of laboratory animals in various functional conditions of nonspecific protective systems. Biophysics 2014; 59(4): 620-627. https://doi.org/10.1134/S0006350914040186

Baryshev MG, Basov AA, Bolotin SN et al. NMR, EPR, and Mass Spectroscopy Estimates of the Antiradical Activity of Water with Modified Isotope Composition. Bulletin of the Russian Academy of Sciences. Physics 2012; 76(12): 1349-1352.

Beers R, Sizer I. Spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J. Biol. Chem 1952; 195: 133-140.

Kostyuk VA, Potapovich AI, Kovaleva ZhV. A simple and sensitive method for determining superoxide dismutase, based on the reaction of oxidation of quercetin. Questions of medical chemistry 1990; 36(2): 88-91.

Robyt JF, Ackerman RJ, Chittenden CG. Reaction of protein disulfide groups with Ellman’s reagent: a case study of the number of sulfhydryl and disulfide groups in Aspergillus oryzae ?-amylase, papain and lysozyme. Arch. Biochem. Biophys 1971; 147: 262-269.

Karpischenko AI. Medical laboratory technologies. Directory. Intermedika, St. Petersburg 2002: 600.

Ellman GL. Tissue sulfhydryl gr?ups. Arch. Bi??h. Bi??hys 1959; 82: 70-77.

Ushkalova BH, Ioanidis HB, Kadochnikova GD et al. Control of lipid peroxidation. Novosibirsk University Press, Novosibirsk 1993: 182.

Yashin AY. A flow-injection system with amperometric detection for selective determination of antioxidants in foodstuffs and drinks. Russian Journal of General Chemistry 2008; 78(12): 2566-2571. https://doi.org/10.1134/S1070363208120360

Basov ??, Baryshev ?G, Dzhimak SS et al. The effect of consumption of water with modified isotope content on the parameters of free radical oxidation in vivo. Fiziolohichny? Zhurnal 2013; 59(6): 49-56.

Proskurnina EV, Polimova AM, Sozarukova MM et al. Kinetic chemiluminescence as a method for oxidative stress evaluation in examinations of patients with type 2 diabetes mellitus. Bulletin of Experimental Biology and Medicine 2016; 161(1): 131-133. https://doi.org/10.1007/s10517-016-3362-x

Dzhimak SS, Basov AA, Volchenko NN et al. Changes in the functional activity of mitochondria isolated from the liver of rat that passed the preadaptation to ultra-low deuterium concentration. Doklady Biochemistry and Biophysics 2017. https://doi.org/10.1134/S1607672917050088

Pershin SM, Ismailov ESh, Dibirova MM et al. Multiple increase in productivity of the yeast at reducing the fraction of D2O in water. Doklady Biochemistry and Biophysics 2017. https://doi.org/10.1134/S1607672917050039

Boros LG, D’Agostino DP, Katz HE et al. Submolecular regulation of cell transformation by deuterium depleting water exchange reactions in the tricarboxylic acid substrate cycle. Medical Hypotheses 2016; 87: 69-74. https://doi.org/10.1016/j.mehy.2015.11.016

Vorozhtsova SV, Abrosimova AN, Kulikova EI et al. Modification of the cytogenetic effects of irradiation by water with the reduced content of deuterium and heavy isotopes of oxygen. Radiats Biol Radioecol 2014; 54(1): 21-6.

Grigorenko DY. Peculiarities of the cellular composition of splenic lymphoid tissue in mice after long-term use of light water and irradiation. Morfologiia 2015; 148(4): 19-23.

Balasubramanian B, Pogozelski WK, Tullius TD. DNA strand breaking by the hydroxyl radical is governed by the accessible surface areas of the hydrogen atoms of the DNA backbone. Proc Natl Acad Sci 1998; 95: 9738-43. https://doi.org/10.1073/pnas.95.17.9738

Ingle S, Azad RN, Jain SS et al. Chemical probing of RNA with the hydroxyl radical at single-atom resolution. Nucleic Acids Res 2014; 42: 12758-67. https://doi.org/10.1093/nar/gku934

Olariu L, Petcu M, Tulcan C et al. Deuterium depleted water- antioxidant or prooxidant? Lucrari stiiniifice medicina veterinara 2007; 40: 265-269.

Olariu L, Petcu M, Pup M et al. The influence of the deuterium depleted water in the experimental cadmium chloride intoxication on liver function in rats. Lucrari stiiniifice medicina veterinara 2007; 40: 270-274.

Olariu L, Petcu M, Cuna S et al. Deuterium depleted water behavior in Chromium (VI) intoxicated female rats’. Banat's Journal of Biotechnology 2010; 1(1): 72-75.

Rehakova R, Klimentova J, Cebova M et al. Effect of Deuterium-Depleted Water on Selected Cardiometabolic Parameters in Fructose-Treated Rats. Physiol Res 2016; 65(3): 401-407.

Pechanova O, Simko F. The role of nitric oxide in the maintenance of vasoactive balance. Physiol Res 2007; 56(2): 7-16.

Vrankova S, Barta A, Klimentova J et al. The regulatory role of nuclear factor kappa B in the heart of hereditary hypertriglyceridemic rat. Oxid Med Cell Longev 2016. https://doi.org/10.1155/2016/9814038

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Copyright (c) 2018 Alexander A. Kravtsov , Stanislav V. Kozin , Ekaterina R. Vasilevskaya , Anna A. Elkina , Lilia V. Fedulova , Konstantin A. Popov , Vadim V. Malyshko , Arkady V. Moiseev , Denis I. Shashkov  , Mikhail G. Baryshev