CC..png    

Legal and postal addresses of the publisher: office 1336, 17 Naberezhnaya Severnoy Dviny, Arkhangelsk, 163002, Russian Federation, Northern (Arctic) Federal University named after M.V. Lomonosov

Phone: (818-2) 21-61-21
E-mail: vestnik_med@narfu.ru
https://vestnikmed.ru/en/

ABOUT JOURNAL

Correction of Free Radical Blood Imbalance and Behaviour in Prenatally Stressed Rats with α-Tocopherol. P. 25–34

Версия для печати

Section: Physiology

Download (pdf, 0.5MB )

UDC

618.2:616-008.9:612.398.12:57.024

DOI

10.37482/2687-1491-Z040

Authors

Olʼga N. Kuleshova* ORCID: 0000-0002-1348-4636
David L. Teplyy* ORCID: 0000-0002-5764-6940
Dmitriy D. Teplyy* ORCID: 0000-0002-3484-9710
*Astrakhan State University
(Astrakhan, Russian Federation)
Corresponding author: Olʼga Kuleshova, address: ul. Shaumyana 2, Astrakhan, 414000, Russian Federation; e-mail: pozdniakova_olga@list.ru

Abstract

The research involved female mongrel white rats (n = 16) and their offspring (sexually mature males, n = 75). Pregnant females were divided into 4 groups: control (intact animals), stress (from the 16th to the 19th day of pregnancy females were subjected to 3-hour immobilization in plastic cases), stress+α-tocopherol (against the background of immobilization, females received α-tocopherol at a dose of 1 mg per 100 g of weight starting from the 2nd day of pregnancy), and α-tocopherol (females received α-tocopherol in the same dose and regimen as the group above). The control and stress groups received vegetable oil instead of α-tocopherol. In 3-month-old female offspring, we studied behaviour and determined the levels of products of free radical modification of proteins and lipids, total antioxidant activity as well as superoxide dismutase and ceruloplasmin activity in the blood plasma. Prenatal stress increased the exploratory and motor activity in offspring and modified the level of free radical homeostasis in the serum of male rats: there was an increase in the level of products of oxidative modification of proteins, thiobarbituric acid reactive substances concentration, end products of lipid peroxidation (Schiff bases), total antioxidant activity and ceruloplasmin activity, as well as a decrease in superoxide dismutase activity. Alpha-tocopherol taken by females during pregnancy brought all the oxidation parameters modified by immobilization to the values of the control group; the levels of primary products of oxidative modification of proteins and lipid peroxidation decreased two-fold, compared with the stress group. The activity of superoxide dismutase and ceruloplasmin returned to the control values, but the total antioxidant activity remained at the level of the stress group. Thus, there is reason to assume that α-tocopherol has a significant corrective effect on the intensity of free radical processes in prenatally stressed white male rats.
For citation: Kuleshova O.N., Teplyy D.L., Teplyy D.D. Correction of Free Radical Blood Imbalance and Behaviour in Prenatally Stressed Rats with α-Tocopherol. Journal of Medical and Biological Research, 2021, vol. 9, no. 1, pp. 25–34. DOI: 10.37482/2687-1491-Z040

Keywords

free radical homeostasis, prenatal stress, correction of the consequences of prenatal stress, α-tocopherol, behaviour, male white rats

References

1. Shallie P.D., Naicker T. The Placenta as a Window to the Brain: A Review on the Role of Placental Markers in Prenatal Programming of Neurodevelopment. Int. J. Dev. Neurosci., 2019, vol. 73, pp. 41–49. DOI: 10.1016/j.ijdevneu.2019.01.003
2. Zheng A., Li H., Cao K., Xu J., Zou X., Li Y., Chen C., Liu J., Feng Z. Maternal Hydroxytyrosol Administration Improves Neurogenesis and Cognitive Function in Prenatally Stressed Offspring. J. Nutr. Biochem., 2015, vol. 26, no. 2, pp. 190–199. DOI: 10.1016/j.jnutbio.2014.10.006
3. Smolenskiy I.V., Pritvorova A.V., Ordyan N.E. Vliyanie prenatalʼnogo stressa na okislitelʼnye modifikatsii belkov i aktivnostʼ superoksiddismutazy v mozge i plazme krovi samtsov krys v modeli posttravmaticheskogo stressovogo rasstroystva [Prenatal Stress Changed Protein Oxidative Modifications and Superoxide Dismutase Activity in Brains of Male Rats and Plasma During Posttraumatic Stress Disorder Modelling]. Rossiyskiy fiziologicheskiy zhurnal im. I.M. Sechenova, 2018, vol. 104, no. 11, pp. 1356–1367. DOI: 10.1134/S0869813918110092
4. Kravtsov A.A., Shurygin A.Y., Shurygina L.V., Zlishcheva L.I., Abramova N.O., Khaspekov L.G. Prenatal Action of Lead Acetate on the Antioxidant Glutathione System of the Brain of Newborn Rats in vivo and on Neurite Growth in vitro. Neurochem. J., 2009, vol. 3, no. 3, pp. 196–201. DOI: 10.1134/S1819712409030076
5. Khuzhakhmetova L.K., Teplyy D.L. Osobennosti svobodnoradikalʼnykh protsessov pri immobilizatsionnom stresse u krys v ontogeneze [Features of Free Radical Processes During Immobilization Stress in Rats in Ontogenesis]. Estestvennye nauki, 2016, vol. 57, no. 4, pp. 72–78.
6. Zakharova I.O., Sokolova T.V., Akhmetshina A.O., Avrova N.F. Alpha-Tocopherol Prevents Long-Term Activation of ERK1/2 in Neurons of the Brain Cortex Under Conditions of Oxidative Stress. Neurochem. J., 2015, vol. 9, no. 4, pp. 319–322. DOI: 10.1134/S1819712415040170
7. Zakharova I.O., Sokolova T.V., Avrova N.F. Alpha-Tocopherol Prevents a Dramatic Oxidative Stress-Induced Decline of the BCL-2 Concentration in Cortical Neurons. Neurochem. J., 2016, vol. 10, no. 3, pp. 226–231. DOI: 10.1134/S1819712416030144
8. Nakazawa T., Miyanoki Y., Urano Y., Uehara M., Saito Y., Noguchi N. Effect of Vitamin E on 24(S)-Hydroxycholesterol-Induced Necroptosis-Like Cell Death and Apoptosis. J. Steroid Biochem. Mol. Biol., 2017, vol. 169, pp. 69–76. DOI: 10.1016/j.jsbmb.2016.03.003
9. Shichiri M., Yoshida Y., Ishida N., Hagihara Y., Iwahashi H., Tamai H., Niki E. α-Tocopherol Suppresses Lipid Peroxidation and Behavioral and Cognitive Impairments in the Ts65Dn Mouse Model of Down Syndrome. Free Radic. Biol. Med., 2011, vol. 50, no. 12, pp. 1801–1811. DOI: 10.1016/j.freeradbiomed.2011.03.023
10. Vieira-Filho L.D., Cabral E.V., Santos F.T., Coimbra T.M., Paixão AD. Alpha-Tocopherol Prevents Intrauterine Undernutrition-Induced Oligonephronia in Rats. Pediatr. Nephrol., 2011, vol. 26, no. 11, pp. 2019–2029. DOI: 10.1007/s00467-011-1908-8
11. Vladimirskaya T.E., Shved I.A., Krivorot S.G., Veyalkina N.N., Adamovich A.V. Opredelenie faz estralʼnogo tsikla belykh krys po kletochnomu sostavu vlagalishchnykh mazkov [Determination of the Estrous Cycle Phases of White Rats According to Cellular Makeup of Vaginal Smears]. Vestsі natsyyanalʼnay akademіі navuk belarusі. Seryya bіyalagіchnykh navuk, 2011, no. 4, pp. 88–91.
12. Shalyapina V.G., Zaychenko I.N., Ordyan N.E., Batuev A.S. Izmenenie neyroendokrinnoy regulyatsii prisposobitelʼnogo povedeniya krys posle stressa v pozdnem prenatalʼnom ontogeneze [Changes in the Neuroendocrine Regulation of Adaptive Behavior in Rats Subjected to Stress in the Late Prenatal Ontogenesis]. Rossiyskiy fiziologicheskiy zhurnal im. I.M. Sechenova, 2001, vol. 87, no. 9, pp. 1193–1201.
13. Kaluev A.V., Tuokhimaa P. Suok-test – novaya povedencheskaya modelʼ trevogi [Ropewalking Test as a New Behavioral Model of Anxiety]. Neyronauki, 2005, no. 1, pp. 17–23.
14. Sirota T.V. Use of Nitro Blue Tetrazolium in the Reaction of Adrenaline Autooxidation for the Determination of Superoxide Dismutase Activity. Biochem. (Mosc.) Suppl. Ser. B, 2012, vol. 6, no. 3, pp. 254–260. DOI: 10.1134/S1990750812030134
15. Ten E.V. Ekspress-metod opredeleniya aktivnosti tseruloplazmina v syvorotke krovi [Express Method for Determining Ceruloplasmin Activity in the Blood Serum]. Laboratornoe delo, 1981, no. 6, pp. 334–335.
16. Klebanov G.I., Babenkova I.V., Teselkin Yu.O., Komarov O.S., Vladimirov Yu.A. Otsenka antiokislitelʼnoy aktivnosti plazmy krovi s primeneniem zheltochnykh lipoproteidov [Assessment of Blood Plasma Antioxidant Activity Using Yolk Lipoproteins]. Laboratornoe delo, 1988, no. 5, pp. 59–62.
17. Mihara M., Uchiyama M., Fukuzawa K. Thiobarbituric Acid Value on Fresh Homogenate of Rat as a Parameter of Lipid Peroxidation in Aging, CCl4 Intoxication, and Vitamin E Deficiency. Biochem. Med., 1980, vol. 23, no. 3, pp. 302–311. DOI: 10.1016/0006-2944(80)90040-x
18. Volchegorskiy I.A., Nalimov A.G., Yarovinskiy B.G., Livshits R.I. Sopostavlenie razlichnykh podkhodov k opredeleniyu produktov perekisnogo okisleniya lipidov v geptan-izopropanolʼnykh ekstraktakh krovi [Comparison of Different Approaches to the Determination of Lipid Peroxidation Products in Heptane-Isopropanol Extracts of Blood]. Voprosy meditsinskoy khimii, 1989, vol. 35, no. 1, pp. 127–131.
19. Dubinina E.E., Burmistrov S.O., Khodov D.A., Porotov I.G. Okislitelʼnaya modifikatsiya belkov syvorotki krovi cheloveka, metod ee opredeleniya [Oxidative Modification of Human Blood Serum Proteins and Its Determination Method]. Voprosy meditsinskoy khimii, 1995, vol. 41, no. 1, pp. 24–26.
20. Flerov M.A., Gerasimova I.A., Vʼyushina A.V., Pritvorova A.V. Vliyanie prenatalʼnogo stressa na svobodnoradikalʼnoe okislenie lipidov i belkov i aktivnostʼ superoksiddismutazy v neyronakh i neyroglii kory bolʼshikh polushariy golovnogo mozga krys [Influence of Prenatal Stress on Free Radical Oxidation Lipids and Proteins and Activity of Superoxide Dismutase in Neurons and Glial Cells of the Rat Brain Cortex]. Rossiyskiy fiziologicheskiy zhurnal im. I.M. Sechenova, 2008, vol. 94, no. 4, pp. 406–413.
21. Clarke D.J., Sarkissian L., Todd S.M., Suraev A.S., Bahceci D., Brzozowska N., Arnold J.C. Nrg1 Deficiency Modulates the Behavioural Effects of Prenatal Stress in Mice. Prog. Neuropsychopharmacol. Biol. Psychiatry, 2019, vol. 88, pp. 86–95. DOI: 10.1016/j.pnpbp.2018.06.013
22. Pivina S.G., Fedotova Y.O., Akulova V.K., Ordyan N.E. Effects of Selective Inhibitors of Serotonin Reuptake on the Anxiety Behavior and Activity of the Pituitary-Adrenal System in Prenatally Stressed Male Rats. Neurochem. J., 2011, vol. 5, no. 1, pp. 47–51.
23. Hodes G.E., Epperson C.N. Sex Differences in Vulnerability and Resilience to Stress Across the Life Span. Biol. Psychiatry, 2019, vol. 86, no. 6, pp. 421–432. DOI: 10.1016/j.biopsych.2019.04.028
24. Persson P., Rossin-Slater M. Family Ruptures, Stress, and the Mental Health of the Next Generation. Am. Econ. Rev., 2018, vol. 108, no. 4, pp. 1214–1252.
25. Beketova N.A., Kodentsova V.M., Shilina N.M., Gmoshinskaya M.V., Pereverzeva O.G., Abramova T.V., Georgieva O.V. Vliyanie priema vitaminno-mineralʼnykh kompleksov na biomarkery antioksidantnogo statusa beremennykh zhenshchin [Influence of Intake of Vitamin-Mineral Complexes on Biomarkers of Antioxidant Status in Pregnant Women]. Voprosy detskoy dietologii, 2015, vol. 13, no. 5, pp. 32–37.
26. Salucci S., Ambrogini P., Lattanzi D., Betti M., Gobbi P., Galati C., Galli F., Cuppini R., Minelli A. Maternal Dietary Loads of Alpha-Tocopherol Increase Synapse Density and Glial Synaptic Coverage in the Hippocampus of Adult Offspring. Eur. J. Histochem., 2014, vol. 58, no. 2. Art. no. 2355. DOI: 10.4081/ejh.2014.2355
27. Ivanova A.S., Peretyatko L.P., Sitnikova O.G., Nazarov S.B. Changes in the Mother–Placenta–Fetus System Under the Effect of α-Tocopherol in Albino Rats with Normal Pregnancy. Bull. Exp. Biol. Med., 2015, vol. 159, no. 4, pp. 517–519. DOI: 10.1007/s10517-015-3006-6



Make a Submission


INDEXED IN: 

DOAJ_logo-colour.png

Elibrary.ru

logotype.png

infobaseindex

Логотип.png




Лань

OTHER NArFU JOURNALS: 

Vestnik of NArFU.
Series "Humanitarian and Social Sciences"

Forest Journal 
Лесной журнал 

Arctic and North