The response of fibroblast-derived factor and endostatin to acute rehabilitation of physical activity along with electrical stimulation in infarcted rats

Document Type : Research Paper

Author

Assistant Professor, Department of Exercise Physiology, Arak Branch, Islamic Azad University, Arak, Iran.

Abstract

Introduction
Myocardial infraction is one of the main causes of death in today's society. Rehabilitation changes some markers in this disease. The aim of this research is to investigate the reaction of factor derived from fibroblasts and endostatin to the acute rehabilitation of physical activity along with electrical stimulation in infarcted rats.
Material and Method
In this controlled experimental study with a control group, 50 Wistar rats (8weeks old, 220±15g) were induced with isoproterenol (150mg/kg) to infarction. Then they were randomly divided into 5 groups of 10 healthy, infarct, rehabilitation, electrical stimulation and rehabilitation with electrical stimulation. The intervention groups underwent increasing rehabilitation (with a speed of 10 to 18m/min and duration of 50m) and electrical stimulation (a foot shock with an intensity of 0.5 M/A and duration of 20m) for one session. After exercise and anesthesia, venous blood samples were collected for FGF-2 and Ens serum levels and evaluated by ELISA method. ANOVA was used for data analysis at a significance level of P<0.05.
Results
Induction of rats with isoproterenol led to a significant increase in the serum levels of FGF-2 and Ens in all groups (P=0.0001). ANOVA showed that a session of rehabilitation led to a significant increase (P=0.040) of serum FGF-2 levels and a non-significant decrease (P=0.547) of Ens in all groups compared to infarction.
Conclusion
It seems that increasing acute rehabilitation by creating positive angiogenic changes in infarcted rats can play an important role in improving myocardial damage and replacing closed capillaries.
Key words

Keywords

Main Subjects


  1. Virani SSA AA, H.J.; Benjamin, E.J.; Bittencourt, M.S.; Callaway, C.W.; Carson, A.P.; Chamberlain, A.M.; Cheng, S.; Delling, F.N.; et al. . . Heart Disease and Stroke Statistics-2021 Update: A Report From the American Heart Association. Circulation Journal. 2021;143:e254-e743.
  2. Tsao CW AA, Almarzooq ZI, Anderson CAM, Arora P, Avery CL, Baker-Smith CM, Beaton AZ, Boehme AK, Buxton AE, Commodore Mensah Y, Elkind MSV, Evenson KR, Eze-Nliam C, Fugar S, Generoso G, Heard DG, Hiremath S, Ho JE, Kalani R, Kazi DS, Ko D, Levine DA, Liu J, Ma J, Magnani JW, Michos ED, Mussolino ME, Navaneethan SD, Parikh NI, Poudel R, Rezk-Hanna M, Roth GA, Shah NS, St-Onge M-P, Thacker EL, Virani SS, Voeks JH, Wang N-Y, Wong ND, Wong SS, Yaffe K, Martin SS; . on behalf of the American Heart Association Council on Epidemiology and Prevention Statistics Committee and Stroke Statistics Subcommittee. Heart disease and stroke statistics—2023 update: a report from the American Heart Association Circulation. 2023.
  3. Estruch R RE S-SJ, Covas M-I, Corella D, Arós F, et al. . Primary prevention of cardiovascular disease with a Mediterranean diet. New England Journal of Medicine. 2013;368(14):1279-90. .
  4. Vahanian A FR. Universal definition of myocardial infarction. In:European Society of Cardiology, editor. ESC guidelines desk reference 2010: Compendium of abridged esc guidelines 2010. London: . Springer Healthcare Ltd; . 2010.
  5. Gavin T DJ, Kubik C, Pofahl W, Hickner R. . Acute resistance exercise increases skeletal muscle angiogenic growth factor expression. Acta physiol. 2007;191(2):139-46.
  6. T. Angiogenesis in lung development, injury and repair: implications for chronic lung disease of prematurity. Neonatology. 2007;91(4):291-7. .
  7. Falk E SP, Fuster V. Coronary plaque disruption. Circulation research. 1995;92(3):657-71.
  8. Okada M OY, Yamawaki H. . Endostatin stimulates proliferation and migration of adult rat cardiac fibroblasts through PI3K/Akt pathway. . European journal of pharmacology. 2015;750:20-6.
  9. Cao R BE, Wahlestedt C, Thyberg J, Cao Y. . Leptin induces vascular permeability and synergistically stimulates angiogenesis2001 98(11):6390–5.
  10. Mirzaei Amirabad G AMR RM. The Effect of Exercise with Different Intensity and Volume on fibroblast growth factor (FGF-2) Gene Expression in Subcutaneous and Visceral Adipose tissue in Male Rats. J Of Sport and Exercise Physiology 2018;11(2):103-16.
  11. Christiaens V LH. Angiogenesis and development of adipose tissue. Mol Cell Endocrinol. 2010;318(1):2-9.
  12. Turner M CA, Stanley J, Watson H. . The fibroblast growth factor family: Neuro modulation of affective behavior. Neuron 2012;76(1):160-74.
  13. Li H. LS, Shao J., Lin X., Cao Y., Jiang W., . Pharmacokinetic and pharmacodynamic study of intratumoral injection of an adenovirus encoding endostatin in patients with advanced tumors. . Gene Therapy 2008;15((4):247-56.
  14. Sponder M C, Ioana-Alexandra, Emich, Michael, Fritzer-Szekeres, Monika, Litschauer, Brigitte, Bergler-Klein, Jutta, Graf, Senta, Strametz-Juranek, Jeanette . (). . Endurance training significantly increases serum endocan but not osteoprotegerin levels: a prospective observational study. . BMC Cardio Disorders. 2017;17(3).
  15. Khalafi M, Malandish, A., Rosenkranz, S.K., Ravasi, A.A., . Effect of resistance training with and without caloric restriction on visceral fat: a systemic review and meta-analysis. . Obes Rev. 2021;22(9):e13275.
  16. Li D-J FH, 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: clinical and experimental 2016;65(5):747-56.
  17. Cheragh Birjandi S SM, Hedayati M. Effect of high intensity interval training and L-Arginine supplementation on serum levels of fibroblast growth factor 21 and atrial natriuretic peptide in overweight and obese young men. . . Journal of Birjand University of Medical Sciences 2016;23(3):211-21. (Persian).
  18. MalekiPoya M AB, Palizvan MR, Saremi A. . Effect of an incremental aerobic training program on improving angiogenesis and balance in vascular endothelial growth factor and endostatinic in male rats with myocardial infarction. Feyz 2019;23(4):407-14.
  19. Patterson CaR, M. S. Therapeutic angiogenesis: the new electrophysiology? Circulation. 1999;99(20):2614-6.
  20. Dobsk P NM, Siegelov J, et al. Low-frequency electrical stimulation increases muscle strength and improves blood supply in patients with chronic heart failure. . Circ J. 2006;70(1):75-82.
  21. Bertinchant J RE, Polge A, Marty-Double C, Fabbro-Peray P, Poirey S, et al. . Comparison of the diagnostic value of cardiac troponin I and T determinations for detecting early myocardial damage and the relationship with histological findings after isoprenaline-induced cardiac injury in rats. Clin Chim Acta. 2000;298((1-2).):13-28.
  22. Malekipooya M KM, Palizvan MR, Saremi A, Abedi B. Changes in Serum Troponin-I and. Changes in Serum Troponin-I and Corticosterone Levels after a Period of Endurance Training and Electrical Stimulation in Infarcted Rats. . Razi J Med Sci. 2021;28(12):271-80 [Persian[.
  23. MalekiPooya M KM, Moradi M, Sayyah M. Acute response of exercise rehabilitation with electrical stimulation on serum levels antigen, carbohydrate 125 (CA-125) and cystatin (Cys-C) in myocardial infarction rats. . Feyz 2022;26(2):147-55 [Persian[.
  24. Schefer V TM. Oxygen consumption in adult and AGED C57BL/6J mice during acute treadmill exercise of different intensity. Exp Gerontol. 1996;31(3):387-92.
  25. Maleki Poya M. AB, Palizvan MR., et al. . The Effect of Eight Weeks of Incremental Endurance Training on The Levels of Matrix Metalloproteinase-1 (MMP1) and Thrombosponidine-1 (TSP1) in the Rats, Induced by Myocardial Infarction by Isoproterenol. J Arak Uni Med Sci. 2019;22(3):118-28. [Persian].
  26. Shen M YM, Qiu C, Zhang G, Li J, Fang W, et al. . Myocardial angiogenesis induced by exercise training involves a regulatory mechanism mediated by kinin receptors. . Clin Exp Hypertens. 2021;43(5):408-15. .
  27. Raju R PSM, Sandhya V.K, Sahu A, Alipoor A, Balakrishnan L, at all. . A network map of FGF-1/FGFR signaling system. J Signal Transduct. 2014:962962.
  28. Mirzaei Amirabad G AMR, Rahimi M. . The Effect of Exercise with Different Intensity and Volume on fibroblast growth factor (FGF-2) Gene Expression in Subcutaneous and Visceral Adipose tissue in Male Rats. J Of Sport and Exercise Physiology. 2018;11(2):103-16.
  29. Sarikhani N QM, Malekipooya M. . The effect of exercise activity with different intensity and volume on the expression of PDGF-B and FGF-2 genes in subcutaneous fat tissue of Wistar rats. Journal of Faculty of Medicine, , ; . Mashhad University of Medical Sciences. 2022;65(3):1259-67.
  30. Khadivi Borujeny A MM, Haghjooy Javanmard Sh, Rajabi H,Khadivi Burojeny Z, Khorshidi Behzadi Mahd. . Effect of Eight Weeks of Resistance Training on Some Signaling Factors Affecting on the Satellite Cells in Wistar Rats. Journal of Isfahan Medical School 2012;30(207).
  31. Ardakanizade M RK, Nazem F. . The effect of ten factors of endurance activity on the gene expression of factors involved in the process of skeletal muscle angiogenesis after myocardial infarction in rats. Koomesh. 2017;19(1):84-92.
  32. Cheragh Birjandi S SM, Hedayati M. Effect of high intensity interval training and L-Arginine supplementation on serum levels of fibroblast growth factor 21 and atrial natriuretic peptide in overweight and obese young men. . Journal of Birjand University of Medical Sciences ; (): [Persian]. 2016;23(3):211-21.
  33. Nameni F NMMS. The effect of endurance resistance exercise combined with Lcitrulline malate supplement on FGF, VEGF, and fatigue among young bodybuilders. . Ebnesina J. 2020;21(4).
  34. Karnoub AE WR. Ras oncogenes: split personalities. Nat Rev Mol Cell Biol. . 2008; 9(7):517-31.
  35. Sponder M, Campean IA, Emich M, Fritzer-Szekeres M, Litschauer B, Graf S, et al. Long-term physical activity leads to a significant increase in serum sRAGE levels: a sign of decreased AGE-mediated inflammation due to physical activity? Heart and vessels. 2018;33(8):893-900.
  36. Gu J-W, Shparago M, Tan W, Bailey AP. Tissue endostatin correlates inversely with capillary network in rat heart and skeletal muscles. Angiogenesis. 2006;9(2):93-9.
  37. Suhr F, Rosenwick C, Vassiliadis A, Bloch W, Brixius K. Regulation of extracellular matrix compounds involved in angiogenic processes in short- and long-track elite runners. Scandinavian journal of medicine & science in sports. 2010;20(3):441-8.
  38. Motahari Rad M AHSRRoVEGFaEtaSAbaaaPoL-ASiAM. Arak Medical University Journal (AMUJ) Original Article 2017;20(119):78-88.
  39. J S. L-Arginine and L-Ornithine Supplementation Facilitates Angiogenesis and Causes Additional Effects on Exercise induced Angiogenesis in Hind-leg Muscles. Advances in exercise and sports physiology. 2009;15(3):101-8.
  40. Nourshahi M, Farahmand F, Bigdeli MR. Effect of cinnamon-extract supplementation on VEGF and Endostatin level in hind leg muscle of aged rats after one session of exhaustive exercise. Iranian Journal of Physiology and Pharmacology. 2017;1(3):184-76.
  41. Noris M, Morigi M, Donadelli R, Aiello S, Foppolo M, Todeschini M, et al. Nitric oxide synthesis by cultured endothelial cells is modulated by flow conditions. Circulation research. 1995;76(4):536-43.
  42. Okada M, Oba Y, Yamawaki H. Endostatin stimulates proliferation and migration of adult rat cardiac fibroblasts through PI3K/Akt pathway. European journal of pharmacology. 2015;750:20-6.
  43. Song XM WX, Li JG, Le LL, Liang H, Xu Y, et al. . The effect of electroacupuncture at ST36 on severe thermal injury-induced remote acute lung injury in rats. Burns. 2015;41:1449–58. .
  44. Sun X LM, Shen D, Hu L, Cai RL, Wu ZJ, et al. . Effects of Acupuncture Neiguan (PC 6) and Xinshu (BL 15)on the expression of MMP-9 with coronary heart disease rats. J Tradit Chin Med. 2013;036:5–9.