Menu

A+ A A-

Download article

DOI: https://doi.org/10.22263/2312-4156.2022.2.35

Kuzhel O.P.
Fish oil prevents the development of arterial hypotension in rats with post-traumatic stress disorder
Vitebsk State Order of Peoples’ Friendship Medical University, Vitebsk, Republic of Belarus

Vestnik VGMU. 2022;21(2):35-44.

Abstract.
Objectives. To evaluate the nature and mechanisms of the protective effect of fish oil (FO) on systemic hemodynamics in rats with an experimental analogue of post-traumatic stress disorder (PTSD).
Material and methods. The studies were carried out on 50 outbred white male rats weighing 210-240 g, divided into groups: «Control», «PTSD», «FO», «FO+PTSD». An analogue of PTSD was reproduced by rats contacting with cat feces for 10 days for 15 minutes daily. Fish oil was administered intragastrically in doses of 0.2 ml (100 mg/kg body weight of eicosapentaenoic (EPA) and docosahexaenoic (DHA) acids, CJSC «Biosola», Lithuania) 3 days before modelling PTSD and during 10 days of stressor action. After 2 weeks, systolic, diastolic, mean arterial blood pressure (SBP, DBP, MAP) and heart rate (HR) were measured by a non-invasive method. The concentration of endothelial NO-synthase (eNOS), inducible NO-synthase (iNOS), corticosterone, C-reactive protein (C-RP), interleukin-1β (IL-1β) was determined in blood serum by enzyme-linked immunosorbent assay (ELISA); spectrophotometric method was used to determine the concentration of malondialdehyde (MDA), diene conjugates (DC), as well as the activity of catalase (CAT) and superoxide dismutase (SOD).
Results. In animals with PTSD, there was a decrease in SBP, DBP and MAP by 18-23% and an increase in heart rate by 20%. The concentration of eNOS in the blood of rats with PTSD decreased by 28%, and iNOS increased 2.28 times, along with 3.3 and 3.6 times increase in the content of DC and MDA against the background of the decreased SOD activity by 27%, CAT by 59% and 1.6 and 3 times increase in the concentration of C-RP and IL-1β, respectively, compared with the control. The introduction of FO either prevented or significantly limited the severity of the detected changes.
Conclusions. The introduction of fish oil to rats prevents the development of arterial hypotension, as well as the changes in the concentration of eNOS and iNOS, it also prevents the disruption of the prooxidant-antioxidant status of blood serum, and reduces the severity of systemic inflammation in animals with PTSD.
Key words: post-traumatic stress disorder, fish oil, arterial blood pressure, nitric oxide, prooxidant-antioxidant status.

References

1. Khozhenko EV. Neural mechanisms of formation of basic clinical syndromes in post-traumatic stress disorder. Klin Medicina. 2009;87(4):4-9. (In Russ.)
2. Blizniuk AI. Post Traumatic Stress Disorder in Combatants: Clinic, Diagnosis, and Correction. Voen Medicina. 2006;(1):31-40. (In Russ.)
3. Selye H. The Physiology and Pathology of Exposure to Stress. A Treatise Based on the Concept of the General Adaptation Syndrome and the Diseases of Adaptation. Inc. Med Gaz. 1952 Sep;87(9):431.
4. Richter-Levin G, Stork O, Schmidt MV. Animal models of PTSD: a challenge to be met. Mol Psychiatry. 2019;24:1135-56.
5. Korkushko OV, Shatilo VB, Ishchuk VA. Use of omega-3 polyunsaturated fatty acids for normalization of endothelial function and blood rheological parameters in pathology of the cardiovascular system. Ukr Med Chasop. 2010;(2):46-9. (In Russ.)
6. Tseilikman OB, Lapshin MS, Komelkova MV, Kondashevskaya MV, Dremencov E, Manukhina EB, et al. Adrenal insufficiency in rats after prolonged exposure to the predator cue: A new animal model of post-traumatic stress disorder . Psychoneuroendocrinol. 2017;83:1-83. doi: http://dx.doi.org/10.1016/j.psyneuen.2017.07.460
7. Melnikov AV, Kulikov MA, Novikova MR, Sharova EV. Selection of behavioral test indicators for assessing the typological features of rat behavior. Zhurn Vyssh Nerv Deiatel'nosti IP Pavlova. 2004;54(5):712-7. (In Russ.)
8. Andreeva LI, Kozhemiakin LA, Kishkun AA. Modification of the method for the determination of lipid peroxides in the thiobarbituric acid test. Lab Delo. 1988;(11):41-3. (In Russ.)
9. Gavrilov VB, Gavrilova AR, Khmara NF. Measurement of diene conjugates in plasma by ultraviolet absorption of heptane and isopropyl acid extracts. Lab Delo. 1988;(2):60-4. (In Russ.)
10. Kostiuk VA, Potapovich AI, Kovaleva ZhV. A simple and sensitive method for determining superoxide dismutase activity based on the oxidation reaction of quercetin. Vopr Med Khimii. 1990;36(2):88-91. (In Russ.)
11. Zoladz PR, Fleshner M, Diamond DM. Differential effectiveness of tianeptine, clonidine and amitriptyline in blocking traumatic memory expression, anxiety and hypertension in an animal model of PTSD. Prog Neuropsychopharmacol Biol Psychiatry. 2013 Jul;44:1-16. doi: http://dx.doi.org/10.1016/j.pnpbp.2013.01.001
12. Cruz FC, Duarte JO, Leão RM, Hummel LFV, Planeta CS, Crestani CC. Adolescent vulnerability to cardiovascular consequences of chronic social stress: Immediate and long-term effects of social isolation during adolescence. Dev Neurobiol. 2016 Jan;76(1):34-46. doi: http://dx.doi.org/10.1002/dneu.22297
13. McDougall SJ, Paull JR, Widdop RE, Lawrence AJ. Restraint stress: differential cardiovascular responses in Wistar-Kyoto and spontaneously hypertensive rats. Hypertension. 2000 Jan;35(1 Pt 1):126-9. doi: http://dx.doi.org/10.1161/01.hyp.35.1.126
14. Silverman MN, Sternberg EM. Glucocorticoid regulation of inflammation and its behavioral and metabolic correlates: from HPA axis to glucocorticoid receptor dysfunction. Ann N Y Acad Sci. 2012 Jul;1261:55-63. doi: http://dx.doi.org/10.1111/j.1749-6632.2012.06633.x
15. Sapolsky RM, Romero LM, Munck AU. How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions. Endocr Rev. 2000 Feb;21(1):55-89. doi: http://dx.doi.org/10.1210/edrv.21.1.0389
16. Rosen RL, Levy-Carrick N, Reibman J, Xu N, Shao Y, Liu M, et al. Elevated C-reactive protein and posttraumatic stress pathology among survivorsof the 9/11 World Trade Center attacks. J Psychiatr Res. 2017 Jun;89:14-21. doi: http://dx.doi.org/10.1016/j.jpsychires.2017.01.007
17. Terock J, Hannemann A, Van der Auwera S, Janowitz D, Spitzer C, Bonk S, et al. Posttraumatic stress disorder is associated with reduced vitamin D levels and functional polymorphisms of the vitamin D binding-protein in a population-based sample. Prog Neuropsychopharmacol Biol Psychiatry. 2020 Jan;96:109760. doi: http://dx.doi.org/10.1016/j.pnpbp.2019.109760
18. Lazuko SS, Beliaeva LE, Solodkov AP. Specific role of induced NO synthase in the mechanisms of regulation of coronary vascular tone in rats under immobilization stress developing against the background of diabetes mellitus. Ros Fiziol Zhurn IM Sechenova. 2014;100(4):433-44. (In Russ.)
19. Halliwell B. Reactive species & antioxidants. Redox biology is a fundamental theme of aerobic life. Plant Physiol. 2006 Jun;141(2):312-22. doi: http://dx.doi.org/10.1104/pp.106.077073
20. Stebbins CL, Stice JP, Hart CM, Mbai FN, Knowlton AA. Effects of dietary decosahexaenoicacid (DHA) on eNOS in human coronary artery endothelial cells. J Cardiovasc Pharmacol Ther. 2008 Dec;13(4):261-8. doi: http://dx.doi.org/10.1177/1074248408322470
21. Abdolahi M, Jafarieh A, Sarraf P, Sedighiyan M, Yousefi A, Tafakhori A, et al. The Neuromodulatory Effects of ω-3 Fatty Acids and Nano-Curcumin on the COX-2/ iNOS Network in Migraines: A Clinical Trial Study from Gene Expression to Clinical Symptoms. Endocr Metab Immune Disord Drug Targets. 2019;19(6):874-884. doi: http://dx.doi.org/10.2174/1871530319666190212170140
22. Heshmati J, Morvaridzadeh M, Maroufizadeh S, Akbari A, Yavari M, Amirinejad A, et al. Omega-3 fatty acids supplementation and oxidative stress parameters: A systematic review and meta-analysis of clinical trials. Pharmacol Res. 2019 Nov;149:104462. doi: http://dx.doi.org/10.1016/j.phrs.2019.104462
23. Asari MA, Zulkaflee MH, Sirajudeen KNS, Yusof NAM, Sairazi NSM. Tualang honey and DHA-rich fish oil reduces the production of pro-inflammatory cytokines in the rat brain following gexposure to chronic stress. J Taibah Univ Med Sci . 2019 Jul;14(4):317-323. doi: http://dx.doi.org/10.1016/j.jtumed.2019.06.004
24. Beliaeva LE, Pavliukevich AN. Early human disease programming and the use of nutraceuticals for preventive purposes: a focus on fish oil. Literature review. Vestn VGMU. 2019;18(5):12-25. (In Russ.)

Information about authors:
Kuzhel O.P. – senior lecturer of the Chair of Normal Physiology, Vitebsk State Order of Peoples’ Friendship Medical University.

Correspondence address: Republic of Belarus, 210009, Vitebsk, 27 Frunze ave., Vitebsk State Order of Peoples’ Friendship Medical University, Chair of Normal Physiology. E-mail: Этот адрес электронной почты защищён от спам-ботов. У вас должен быть включен JavaScript для просмотра. – Olga P. Kuzhel.

Поиск по сайту