The Effect of Interval Training on Cardiac Angiogenesis Capacity in Rats with Myocardial Infarction
الموضوعات :
Report of Health Care
Mehran Ghahramani
1
,
Sara Karbalaeifar
2
1 - Department of Physical Education, Gilan-E-Gharb, Islamic Azad University, Gilan-E-Gharb,Iran.
2 - Department of Physical Education University of Tehran, Kish International Campus, Kish, Iran.
تاريخ الإرسال : 17 الثلاثاء , رجب, 1439
تاريخ التأكيد : 28 الإثنين , محرم, 1440
تاريخ الإصدار : 25 الثلاثاء , ربيع الثاني, 1440
الکلمات المفتاحية:
Training,
Myocardial Infarction,
VEGF,
collagen 18,
Flt-1,
ملخص المقالة :
Introduction: Myocardial infarction (MI) is the destruction and permanent and irreversible cell death of part of the cardiac muscle (myocardium) which occurs due to loss of blood flow to the heart. The condition disrupts individuals’ daily life and limits their performance. Evidence indicates the likely effect of exercise on increasing the capillary density of skeletal muscle and myocardium. Vascular endothelial growth factor (VEGF) and endostatin as well as their common receptors (Flt-1) are the most important factors involved in angiogenesis. Therefore, this research aimed to evaluate the effect of 6 weeks of interval training on the VEGF, Flt-1 and collagen 18 in rats with MI. Methods: 12 male Wistar rats with mean age of 10weeks and average weight of 250- 300 gr were infected with myocardial infarction and were assigned into two groups of (1) experimental (60 minutes of interval running on treadmill, each interval 4 minutes with the 60- 75 percent of Vo2max and 2 minutes of active rest at 50- 60 percent of Vo2max for four days in a week for a period of 6 weeks) and (2) control group (without any training). Gene expression was investigated by the PCR technique and Ejection fraction and Shortening fraction were investigated by echocardiograph. Data were analyzed by SPSS 18 using independent samples t-test (p≤0.05). Results: Results showed that low intensity interval training had a significant effect on increasing the expression level of Flt-1 (P=0.02) and VEGF (P=0.01) genes and no significant change in collagen 18 (P=0.34). Conclusion: The overall results of the study supported the role of low-intensity interval training in increasing the basic factors affecting the process of angiogenesis after MI.
المصادر:
Gavin TP, Stallings HW, Zwetsloot KA, Westerkamp LM, Ryan NA, Moore RA, Pofahl E, Hickner RC. Lower capillary density but no difference in VEGF expression in obese vs lean young skeletal muscle in humans. J Appl Physiol. 2005; 98: 315- 323.
Prior BM, Yang HT, Terjung RL. What makes vessels grow with exercise training? J Appl Physiol. 2004; 97: 1119- 1128.
Lloyd PG, Prior BM, Yang HT, Terjung RL. Angiogenic growth factor expression in rat skeletal muscle in response to exercise training. Am J Physiol Heart Circ Physiol. 2003; 284: 1668- 1678.
Bates DO. Vascular endothelial growth factors and vascular permeability. Cardiovas Res. 2010; 87: 262- 271.
Sugiyama A, Hirano Y, Okada M, Yamawaki H. Endostatin stimulates proliferation and migration of myofibroblasts isolated from myocardial infarction model rats. Int J Mol Sci. 2018; 19 (741): 1- 15.
Mooren F, Völker K. Molecular and cellular exercise physiology. Human Kinetics. 2004; 451.
Brixius K, Schoenberger S, Ladage D, Knigge H, Falkowski G, Hellmich M, et al. Long-term endurance exercise decreases antiangiogenic endostatin signalling in overweight men aged 50-60 years. Br J Sports Med. 2008; 42: 126- 129.
Hyuek Jong L. Exercise training regulates angiogenic gene expression in white adipose tissue. J Exerc Rehabil. 2018; 14 (1): 16- 23.
Olivier JG, Koulmann N, Peinnequin A, Xavier AB. Exercise‐ induced expression of vascular endothelial growth factor mRNA in rat skeletal muscle is dependent on fiber type. J Physiol. 2003; 552 (1): 213- 221.
Gu JW, Gadonski G, Wang J, Makey I, Adair TH. Exercise increases endostatin in circulation of healthy volunteers. BMC Physiol. 2004; 16: 2- 4.
Rullman E, Rundqvist H, Wågsäter D, Fischer H, Eriksson P, Sundberg CJ, et al. A single bout of exercise activates matrix metalloproteinase in human skeletal muscle. J Appl Physiol. 2007; 102: 2346- 2351.
Frisbee JC, Samora JB, Peterson J, Bryner R. Exercise training blunts microvascular rarefaction in the metabolic syndrome. Am J Physiol Heart Circ Physiol. 2006; 291: 2483- 2492.
Kimura H, Weisz A, Kurashima Y, Hashimoto K, Ogura T, D'Acquisto F, et al. Hypoxia response element of the human vascular endothelial growth factor gene mediates transcriptional regulation by nitric oxide: control of hypoxia-inducible factor-1 activity by nitric oxide. Blood J. 2000; 95 (2): 189- 197.
Lloyd PG, Yang HT, Terjung RL. Arteriogenesis and angiogenesis in rat ischemic hindlimb: role of nitric oxide. Am J Physiol Heart Circ Physiol. 2001; 286 (6): 2528- 2538.
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. Scand J Med Sci Sports. 2010; 20: 441- 448.
Seida A, Wada J, Kunitomi M, Tsuchiyama Y, Miyatake N, Fujii M, et al. Serum bFGF levels are reduced in Japanese overweight men and restored by a 6-month exercise education. Int J Obes Relat Metab Disord. 2003; 27: 1325- 1331.
Zhang R, Wang L, Zhang L, Chen J, Zhu Z, Zhang Z, Chopp M. Nitric oxide enhances angiogenesis via the synthesis of vascular endothelial growth factor and cGMP after stroke in the rat. Cir Res. 2003; 92 (3): 308- 313.
Iemitsu M, Maeda S, Jesmin S, Otsuki T, Miyauchi T. Exercise training improves aging-induced downregulation of VEGF angiogenic signaling cascade in hearts. Am J Physiol Heart Circ Physiol. 2006; 291: 1290- 1298.
Dinenno FA, Tanaka H, Monahan KD, Clevenger CM, Eskurza I, DeSouza CA, et al. Regular endurance exercise induces expansive arterial remodelling in the trained limbs of healthy men. J Physiol. 2001; 534 (1): 287- 295.
Hudlicka O, Brown MD. Adaptation of skeletal muscle microvasculature to increased or decreased blood flow role of shear stress nitric oxide and vascular endothelial growth factor. J Vasc Res. 2009; 46: 504- 512.
Holloszy, John O, and Edward F. Adaptations of skeletal muscle to endurance exercise and their metabolic consequence. Exe Physiol. 2000; 56 (4): 831- 838.
Nakatani A, Han D, Hansen PA, Nolte LA, Host HH, Hickner RC, et al. Effect of endurance exercise training on muscle glycogen supercompensation in rats. J Appl Physiol. 1997; 82 (2): 711- 715.
Leslie AC, Jennifer L. Endogenous anabolic hormone responses to endurance versus resistance exercise and training in women. J Sports Med. 2012; 32 (1): 1- 22.
Koos BJ, Adenosine A. A receptors and O (2) sensing in development. Am J Physiol Regul Integr Comp Physiol. 2011; 301: 601- 622.
Ribatti D, Crivellato E. Mast cells, angiogenesis, and tumor growth. Biochim Biophys Acta. 2012; 1822: 2- 8.
Folkman J. Fundamental concepts of the angiogenic process. Curr Mol Med. 2003; 7 (3): 643- 651.