Evaluation of neurological deficiency in rats with cerebral ischaemia following the administration of omega polyunsaturated fatty acids

Authors

DOI:

https://doi.org/10.20883/medical.e529

Keywords:

cerebral ischaemia, rats, neurological deficiency, omega-3 polyunsaturated fatty acids

Abstract

Aim. The aim of the study was to assess the degree of neurological deficit in rats with experimental cerebral ischaemia following the administration of omega-3 polyunsaturated fatty acids.
Material and Methods. The experiments were conducted on 42 male outbred white rats weighing 260 ± 20 g. The modelling of cerebral ischaemia was performed with intravenous thiopental anaesthesia (40-50 mg / kg), and the research involved models of subtotal, partial and stepwise subtotal cerebral ischaemia. Subtotal cerebral ischaemia (SCI) was modelled by simultaneous ligation of both common carotid arteries (CCA). Partial cerebral ischaemia (PCI) was modelled by ligating one CCA on the right. Stepwise subtotal CI (SSCI) was performed by sequential ligation of both CCA within the intervals of 1 day (subgroup 1), 3 days (subgroup 2), or 7 days (subgroup 3). In order to investigate the effects of omega-3 polyunsaturated fatty acids (ω-3 PUFA), animals with CI were injected intragastrically with the drug "Omegamed" (SCI+ω-3 PUFA) at a dose of 5 g / kg of body weight for the duration of one week. The control group consisted of sham-operated rats of the same sex and weight. Neurological deficits were assessed with regard to the "muscle strength", "swimming test" and "open field" tests after 5-6 hours of the ischaemic period.
Results. Following a stepwise bilateral ligation of both common carotid arteries with a 1 day interval, neurological disorders were most prominent, which indicates an aggravation of neurological deficit with a reduction in the time between CCA dressings. In rats with SCI, the changes were more visible than with PCI, although they were less observable than in the group with SCI. The least noticeable changes were noted in the 3rd subgroup (with a 7 day interval between CCA dressings). Research has demonstrated a dependence of the severity of brain damage in SSCI on the interval between the blood supply cessation in both CCA. In the course of a 7 day interval between CCA dressings, the compensatory mechanisms were activated, which prevented the development of morphological changes and neurological deficits. When CCA was ligated within 1 day interval, the degree of neurological deficit was maximal, indicating an insufficient implementation of compensatory mechanisms. In comparison with the control group, the rats of the "SCI+ω3-PUFA" group retained neurological deficit, the muscle strength indicator was decreased by 86% (p<0.05), the swimming duration by 63% (p<0.05), the number of crossed squares by 55% (p<0.05), the number of washes by 62% (p<0.05), the number of racks by 62.5% (p<0.05) and the number of bowel movements by 60% (p<0.05). However, the neurological deficit was less prominent as compared with the SCI group. In fact, an increase in muscle strength by 67% (p<0.05) was observed, in swimming duration by 37.5% (p<0.05) and in the number of squares crossed in the “open field” test by 31% (p<0.05), which indicates the presence of a corrective action in the ω3-PUFA preparation.
Conclusion. The administration of the preparation of ω-3 polyunsaturated fatty acids has a corrective effect in subtotal cerebral ischaemia, contributing to a reduced severity of the neurological deficit symptoms (an increase in muscle strength, duration of swimming and the number of squares crossed in the “open field” test).

Downloads

Download data is not yet available.

References

Sveinsson OA, Kjartansson O, Valdimarsson E. Cerebral ischaemia/infarction - epidemiology, causes and symptoms. Laeknabladid. 2014;100(5):271–279.

Schaar K. Functional assessments in the rodent stroke model. Experimental & Translational Stroke Medicine. 2010;2: 13–18.

Bon LI, Maksimovich NYe, Zimatkin SM. Effects of experemental cerebral ishemia on metabolic characteristics of parietal cortex neurons. Bioprocess Engineering. 2018;1:1–5.

Bon LI, Maksimovich NYe, Zimatkin SM. Morphological disorders of neurons in the hippocampus of rats with subtotal and total ischaemia. Orenburg Medical Bulletin. 2020;2:41–46.

Chandra A, Stone CR, Li WA, Geng X, Ding Y. The cerebral circulation and cerebrovascular disease II: Pathogenesis of cerebrovascular disease. Brain Circ. 2017;3:57–65.

Chandra A, Stone CR, Li WA, Geng X, Ding Y.The cerebral circulation and cerebrovascular disease III: Stroke. Brain Circ. 2017; 3(2): 66–77.

Bod'ová K. Probabilistic models of individual and collective animal behavior. PLoS One. 2018;7:13–16.

Bon LI, Maksimovich NYe. Methods of estimation of neurological disturbances in experimental cerebral ischaemia. Biomedicine. 2019;2: 69–74.

Chouinard-Thuly L. Technical and conceptual considerations for using animated stimuli in studies of animal behavior. Curr Zool. 2017;63:5–19.

Cinque S. Behavioral Phenotyping of Dopamine Transporter Knockout Rats: Compulsive Traits, Motor Stereotypies, and Anhedonia. Front Psychiatry. 2018;22:9–43.

Fashing PJ. Behavior toward the dying, diseased, or disabled among animals and its relevance to paleopathology. Int J Paleopathol. 2011;1:128–129.

Rosińczuk J. The protective action of tocopherol and acetylsalicylic acid on the behavior of rats treated with dioxins. Adv Clin Exp Med. 2018.;27:5–14

Sestakova N. Determination of motor activity and anxiety-related behaviour in rodents: methodological aspects and role of nitric oxide. Interdisciplinary Toxicology. 2013;6:126–135.

Kaliannan K, Li XY., Wang B, Pan Q, Chen CY., Hao L, Xie S, Kang JX. Multi-omic analysis in transgenic mice implicates omega-6/omega-3 fatty acid imbalance as a risk factor for chronic disease. Commun Biology.2019;1:276–280.

Khunt D, Shrivas M, Polaka S, Gondaliya P, Misra M. Role of Omega-3 Fatty Acids and Butter Oil in Targeting Delivery of Donepezil Hydrochloride Microemulsion to Brain via the Intranasal Route: a Comparative Study. Pharmacology Sciencific Technology. 2020;21:45–50.

Mozaffarian D, Wu JH. Omega-3 fatty acids and cardiovascular disease: effects on risk factors, molecular pathways, and clinical events. J Am Coll Cardiol. 2011; 58: 2047–2067

Tavazzi L, Maggioni AP, Marchioli R, Barlera S. Effect of n-3 polyunsaturated fatty acids in patients with chronic heart failure (the GISSI-HF trial): a randomised, double-blind, placebo-controlled trial. Lancet. 2008; 372:1223–1230

Yokoyama M, Origasa H. Effects of eicosapentaenoic acid on major coronary events in hypercholesterolaemic patients (JELIS): a randomised open-label, blinded endpoint analysis. Lancet. 2007; 369: pp. 1090–1098

Kris-Etherton P, Harris W, Appel L. American Heart Association. Nutrition Committee. Fish consumption, fish oil, omega-3 fatty acids, and cardiovascular disease. Circulation. 2002; 106: 2747–2757

Downloads

Published

2021-09-21

Issue

Section

Original Papers

How to Cite

1.
Bon L, Maksimovich NY. Evaluation of neurological deficiency in rats with cerebral ischaemia following the administration of omega polyunsaturated fatty acids. JMS [Internet]. 2021 Sep. 21 [cited 2024 Nov. 2];90(3):e529. Available from: https://jmsnew.ump.edu.pl/index.php/JMS/article/view/529
Received 2021-06-11
Accepted 2021-09-15
Published 2021-09-21