XML Print


1- Department of Exercise Physiology, Faculty of Sport Sciences, Shahid Chamran University of Ahvaz, Ahvaz, Iran
2- Department of Exercise Physiology, Faculty of Sport Sciences, Shahid Chamran University of Ahvaz, Ahvaz, Iran , hamidhabibi330@gmail.com
Abstract:   (329 Views)
Background: Performing exercise training with various protocols, especially aquatic exercises, can be effective against the harmful effects of Multiple Sclerosis. Therefore, the present study aimed to investigate the effect of six weeks of swimming training on the Caspase-1, TGF-β1, and IFN-γ protein content in the hippocampal tissue of rats with Multiple Sclerosis.
Methods: Twenty-one Wistar rats were divided into three equal groups: (1) Healthy control, (2) Multiple Sclerosis control, and (3) Multiple Sclerosis swimming. After two weeks of adaptation to the laboratory environment, the Multiple Sclerosis groups were induced by adding cuprizone to their diet. Six weeks of swimming training were then performed. Forty-eight hours after the last session, hippocampal tissue was isolated to examine Caspase-1, TGF-β1, and IFN-γ protein content. To analyze the data, one-way analysis of variance was used with a significance level of 0.05.
Results: Findings showed that the induction of Multiple Sclerosis in rats caused a significant increase in TGF-β1 and Caspase-1 protein content (P-Value=0.001) and a significant decrease in IFN-γ (P-Value =0.001). After six weeks of swimming, there was a significant decrease in Caspase-1 (P-Value =0.001) and a significant increase in IFN-γ (P-Value =0.001) protein content; however, there was no significant decrease in TGF-β1 protein content (P-Value =0.1).
Conclusion: Based on the findings of this study, it can be concluded that swimming, as a non-pharmacological intervention, has a protective effect on nerves by reducing factors related to inflammation and cell death, which may have beneficial effects on memory information processing in Multiple Sclerosis disease.

 
     
Type of Article: Original article | Subject: Health
Received: 2025/03/31 | Accepted: 2025/10/15

References
1. Kunkl M, Frascolla S, Amormino C, Volpe E, Tuosto L. T helper cells: the modulators of inflammation in multiple sclerosis. Cells. 2020;9(2):482. [View at Publisher] [DOI] [PMID] [Google Scholar]
2. Haase S, Linker RA. Inflammation in multiple sclerosis. Ther Adv Neurol Disord. 2021;14:17562864211007687. [View at Publisher] [DOI] [PMID] [Google Scholar]
3. Koenig KA, Rao SM, Lowe MJ, Lin J, Sakaie KE, Stone L, et al. The role of the thalamus and hippocampus in episodic memory performance in patients with multiple sclerosis. Mult Scler. 2019;25(4):574-84. [View at Publisher] [DOI] [PMID] [Google Scholar]
4. Rocca MA, Barkhof F, De Luca J, Frisén J, Geurts JJ, Hulst HE, et al. The hippocampus in multiple sclerosis. Lancet Neurol. 2018;17(10):918-26. [View at Publisher] [DOI] [PMID] [Google Scholar]
5. Mancini A, Gaetani L, Di Gregorio M, Tozzi A, Ghiglieri V, Calabresi P, et al. Hippocampal neuroplasticity and inflammation: relevance for multiple sclerosis. Mult Scler Demyelinating Disord. 2017;2(1):1-12. [View at Publisher] [DOI] [Google Scholar]
6. Lorking N, Murray AD, O'Brien JT. The use of positron emission tomography/magnetic resonance imaging in dementia: A literature review. Int J Geriatr Psychiatry. 2021;36(10):1501-13. [View at Publisher] [DOI] [PMID] [Google Scholar]
7. Magliozzi R, Howell OW, Calabrese M, Reynolds R. Meningeal inflammation as a driver of cortical grey matter pathology and clinical progression in multiple sclerosis. Nat Rev Neurol. 2023;19(8):461-76. [View at Publisher] [DOI] [PMID] [Google Scholar]
8. Habibian M, Moosavi SJ. Neuroprotective Effect of Curcumin on Factors Involved in Neurogenesis and Angiogenesis in Aged Brain. 2023. [View at Publisher] [DOI] [Google Scholar]
9. Guevara C, Ortiz FC. Glial-derived transforming growth factor β1 (TGF-β1): A key factor in multiple sclerosis neuroinflammation. Neural Regen Res. 2021;16(3):510-1. [View at Publisher] [DOI] [PMID] [Google Scholar]
10. Bao Y, Liu X, Han C, Xu S, Xie B, Zhang Q, et al. Identification of IFN-γ-producing innate B cells. Cell Res. 2014;24(2):161-76. [View at Publisher] [DOI] [PMID] [Google Scholar]
11. Hussein D, Darweesh M, editors. Role of EBV infection in Type-1 Diabetic nephropathy pathogenesis with related to IL-12 level in patients. BIO Web Conf. 2023;65:05041. [View at Publisher] [DOI] [Google Scholar]
12. Chodzko-Zajko WJ, Proctor DN, Singh MAF, Minson CT, Nigg CR, Salem GJ, et al. American College of Sports Medicine position stand. Exercise and physical activity for older adults. Med Sci Sports Exerc. 2009;41(7):1510-30. [View at Publisher] [DOI] [PMID] [Google Scholar]
13. Jin J-J, Ko I-G, Kim S-E, Shin M-S, Kim S-H, Jee Y-S. Swimming exercise ameliorates multiple sclerosis-induced impairment of short-term memory by suppressing apoptosis in the hippocampus of rats. J Exerc Rehabil. 2014;10(2):69-74. [View at Publisher] [DOI] [PMID] [Google Scholar]
14. Zimmermann J, Emrich M, Krauthausen M, Saxe S, Nitsch L, Heneka MT, et al. IL-17A promotes granulocyte infiltration, myelin loss, microglia activation, and behavioral deficits during cuprizone-induced demyelination. Mol Neurobiol. 2018;55(2):946-57. [View at Publisher] [DOI] [PMID] [Google Scholar]
15. Lubrich C, Giesler P, Kipp M. Motor behavioral deficits in the cuprizone model: validity of the rotarod test paradigm. Int J Mol Sci. 2022;23(19):11342. [View at Publisher] [DOI] [PMID] [Google Scholar]
16. Ghotbeddin Z, Khazaeel K, Tabandeh M-R, Aliheydari M, Yaghoubi H. Effects of omega-3 fatty acid supplementation during chronic maternal hypoxia on behavioral disorders in male rat offspring: The role of Trk family and oxidative stress. Metab Brain Dis.2022;37(6):1959-67. [View at Publisher] [DOI] [PMID] [Google Scholar]
17. Kim J-Y, Yi E-S, Lee H, Kim J-S, Jee Y-S, Kim S-E, et al. Swimming exercise ameliorates symptoms of MOG-induced experimental autoimmune encephalomyelitis by inhibiting inflammation and demyelination in rats. Int Neurourol J. 2020;24(1):S39-47. [View at Publisher] [DOI] [PMID] [Google Scholar]
18. Beheshti M, Salehi Z, Abolfazli R, Shirzad H, Izad M. Increased level of caspase-1 in the serum of relapsing-remitting multiple sclerosis (RRMS) patients. Iran J Allergy Asthma Immunol. 2020;19(5):534-8. [View at Publisher] [DOI] [PMID] [Google Scholar]
19. Hajivand M, Fathi M, Karaji ZG, Rezaei R. the effect of swimming training on the expression of caspase 1 and AIM2 protein in Hippocampus male wistar rats. J Arak Uni Med Sci. 2024;26(6):61-7. [View at Publisher] [DOI] [Google Scholar]
20. Shao Y, Chen C, Zhu T, Sun Z, Li S, Gong L, et al. TRPM2 contributes to neuroinflammation and cognitive deficits in a cuprizone-induced multiple sclerosis model via NLRP3 inflammasome. Neurobiol Dis. 2021;160:105534. [View at Publisher] [DOI] [PMID] [Google Scholar]
21. Yu H, Wu M, Lu G, Cao T, Chen N, Zhang Y, et al. Prednisone alleviates demyelination through regulation of the NLRP3 inflammasome in a C57BL/6 mouse model of cuprizone-induced demyelination. Brain Res. 2018;1678:75-84. [View at Publisher] [DOI] [PMID] [Google Scholar]
22. Liu Y, Fan H, Li X, Liu J, Qu X, Wu X, et al. Trpv4 regulates Nlrp3 inflammasome via SIRT1/PGC-1α pathway in a cuprizone-induced mouse model of demyelination. Exp Neurol. 2021;337:113593. [View at Publisher] [DOI] [PMID] [Google Scholar]
23. Khakroo Abkenar I, Rahmani-Nia F, Lombardi G. The effects of acute and chronic aerobic activity on the signaling pathway of the inflammasome NLRP3 complex in young men. Medicina. 2019;55(4):105. [View at Publisher] [DOI] [PMID] [Google Scholar]
24. Pahlavani HA. Exercise-induced signaling pathways to counteracting cardiac apoptotic processes. Front Cell Dev Biol. 2022;10:950927. [View at Publisher] [DOI] [PMID] [Google Scholar]
25. Golbashi R, Gaeini A, Kordi MR, Aboutaleb N, Ghardashi Afousi A. Effect of one period of high-intensity interval training on myocardial collagen-1 and TGF-β1 and cardiac function in post ischemia-reperfusion rats. Daneshvar Medicine. 2018;26(2):65-74. [View at Publisher] [Google Scholar]
26. Xiong Y, Wang J, Huang S, Cao Y. Investigating the effect of exercise on the expression of genes related to cardiac physiological hypertrophy. Cell Mol Biol (Noisy-le-grand). 2023;69(5):63-9. [View at Publisher] [DOI] [PMID] [Google Scholar]
27. Li D-J, Fu H, Zhao T, Ni M, Shen F-M. Exercise-stimulated FGF23 promotes exercise performance via controlling the excess reactive oxygen species production and enhancing mitochondrial function in skeletal muscle. Metabolism. 2016;65(5):747-56. [View at Publisher] [DOI] [PMID] [Google Scholar]
28. Bjarnadóttir K, Benkhoucha M, Merkler D, Weber MS, Payne NL, Bernard CC, et al. B cell-derived transforming growth factor-β1 expression limits the induction phase of autoimmune neuroinflammation. Sci Rep. 2016;6(1):34594. [View at Publisher] [DOI] [PMID] [Google Scholar]
29. Golzari Z, Shabkhiz F, Soudi S, Kordi MR, Hashemi SM. Combined exercise training reduces IFN-γ and IL-17 levels in the plasma and the supernatant of peripheral blood mononuclear cells in women with multiple sclerosis. Int Immunopharmacol. 2010;10(11):1415-9. [View at Publisher] [DOI] [PMID] [Google Scholar]
30. Kyrkanides S, Tallents RH, Miller J-NH, Olschowka ME, Johnson R, Yang M, et al. Osteoarthritis accelerates and exacerbates Alzheimer's disease pathology in mice.J Neuroinflammation. 2011:8:112. [View at Publisher] [DOI] [PMID] [Google Scholar]
31. Shui L, Yi R-N, Wu Y-J, Bai S-M, Si Q, Bo A-g, et al. Effects of mongolian warm acupuncture on iNOS/NO and inflammatory cytokines in the hippocampus of chronic fatigue rats. Front Integr Neurosci. 2020;13:78. [View at Publisher] [DOI] [PMID] [Google Scholar]
32. Smith PM, Wolcott RM, Chervenak R, Jennings SR. Control of acute cutaneous herpes simplex virus infection: T cell-mediated viral clearance is dependent upon interferon-γ (IFN-γ). Virology. 1994;202(1):76-88. [View at Publisher] [DOI] [PMID] [Google Scholar]
33. Choi E-J, Lee C-J, Park H-H, So W-Y. Effect of 12-week low-intensity exercise on interleukin-2, interferon-gamma and interleukin-4 cytokine production in rat spleens. J Mens Health. 2018;14(3):e14-e9. [View at Publisher] [DOI] [Google Scholar]
34. Smith BC, Sinyuk M, Jenkins JE, Psenicka MW, Williams JL. The impact of regional astrocyte interferon-γ signaling during chronic autoimmunity: a novel role for the immunoproteasome. J Neuroinflammation. 2020;17(1):184. [View at Publisher] [DOI] [PMID] [Google Scholar]

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2025 CC BY-NC 4.0 | Jorjani Biomedicine Journal

Designed & Developed by : Yektaweb