مقایسۀ اثر فشار ا کسایشی ناشی از ده هفته شنای متوسط و طولانیمدت بر رگزایی بطن چپ موشهای صحرایی نر

نوع مقاله : علمی - پژوهشی

نویسندگان

1 گروه علوم ورزشی، دانشکدۀ علوم انسانی، دانشگاه دامغان، دامغان، ایران

2 دانشکدۀ علوم ورزشی، دانشگاه بوعلی سینا، همدان، ایران

چکیده

هدف: در مطالعات پیشین، بین رگ‌زایی و فشار اکسایشی رابطه‌ای عنوان شده است؛ بنابراین، پژوهش حاضر با هدف مقایسۀ اثر دو پروتکل متوسط و طولانی‌مدت بر رگ‌زایی بطن چپ موش‌های صحرایی نر انجام گرفت.
روش‌ها: تعداد 18 سر موش نر صحرایی (20±210 گرم) به‌صورت تصادفی به سه گروه همتای کنترل، شنای متوسط و طولانی‌مدت تقسیم شدند. گروه‌های تمرینی به مدت 10 هفته و 5 روز در هفته در آب 32 درجۀ سانتی‌گراد شنا کردند. در هر جلسه گروه متوسط یک ساعت و گروه طولانی سه ساعت شنا کردند. یک روز پس از پایان تمرین، بافت بطن چپ قلب جدا شد و برای سنجش بیان ژن‌های عامل ‌رشد اندوتلیال‌ عروقی B، عامل ‌رشد فیبروبلاست B، آنژیوپویتین 1و2 و ماتریکس‌ متالوپروتئیناز 2 از روش real-time PCR استفاده شد. تفاوت‌ها با روش آنوا یکطرفه، و مقایسۀ گروه‌ها از طریق آزمون تعقیبی توکی در سطح معناداری 05/0p<  انجام گرفت.
نتایج: مقادیر بیان ژن‌های عامل‌ رشد اندوتلیال ‌عروقی B، آنژیوپویتین 1و2، و ماتریکس ‌متالوپروتئیناز 2 در گروه طولانی‌مدت در مقایسه با هر دو گروه کنترل و متوسط، و در گروه متوسط نیز در مقایسه با گروه کنترل افزایش معناداری یافت، اما بیان ژن عامل ‌رشد فیبروبلاست B فقط در گروه متوسط در مقایسه با گروه کنترل افزایش معناداری داشت (001/0=P).
نتیجه‌گیری: با توجه به افزایش معنادار نیتریک ‌اکسید، می‌توان رخداد فرایند رگ‌زایی در گروه طولانی‌مدت را به فشار برشی، و در گروه متوسط به افزایش معنادار مالون‌ دی‌آلدئید، به فشار اکسایشی نسبت داد.

کلیدواژه‌ها


عنوان مقاله [English]

Comparison of the effects of 10 weeks mid and long-term swimming induced oxidative stress on left ventricular angiogenesis in male rats

نویسندگان [English]

  • Maliheh Ardakani-zadeh 1
  • Leila Vesali-akbarpour 2
1 Department of Sports Science, Faculty of Humanities, Damghan University, Damghan, Iran
2 Faculty of Sports Sciences, Bu Ali Sina University, Hamadan, Iran
چکیده [English]

Purpose: In previous studies, there was a relationship between angiogenesis and oxidative stress thus the aim of this study was to compare the effect of two protocols of mid and long-term on left ventricular angiogenesis in male rats.
Methods:  The 18 male Wistar rats of 210 ± 20g, were randomly assigned in to three equal groups: control, mid and long-term group. Training groups swam in 32֯ water five days per week for 10 weeks. The mid-term group swam for one hour and the long-term group for three hours per session. One day after the end of the protocol, left ventricle of the heart was removed. Real-time PCR method was used to measure the genes expression of Vascular-endothelial-growth-factor-B, Fibroblast-Growth-Factor-B, Angiopoiteine1&2. Differences were determined using by ANOVA One-Way method and the groups were compared by Tukey follow-up test at the significant level of P < 0.05.
Results: The genes expression levels of Vascular-endothelial-growth factor-B, Angiopoiteine1&2 and Matrix-metalloproteinases-2 were significantly increased in the long-term group in compared to the both the control and mid-term groups, and in the mid-term group in compared to the control group, but the gene expression of Fibroblast-Growth-Factor-B had a significant increase only in the mid-term group in compared to the control group (P = 0.001).
Conclusion: Due to the significantly increase of nitric-oxide, the angiogenesis process in the long-term group can be related to shear stress, and in the mid-term group, due to a significant increase in Malondialdehyde, it was attributed to oxidative stress.

کلیدواژه‌ها [English]

  • Oxidative stress
  • Angiogenesis
  • Mid-term swimming
  • Long-term swimming
1. Rinaldi B, Corbi G, Boccuti S, Filippelli W, Rengo G, Leosco D, et al. Exercise training affects age-induced changes in SOD and heat shock protein expression in rat heart. Experimental gerontology. 2006;41(8):764-70.
2. Tofler GH, Muller JE, Stone PH, Forman S, Solomon RE, Knatterud GL, et al. Modifiers of timing and possible triggers of acute myocardial infarction in the Thrombolysis in Myocardial Infarction Phase II (TIMI II) Study Group. Journal of the American College of Cardiology. 1992;20(5):1049-55.
3. Kasap S, Gönenç A, Şener DE, Hisar İ. Serum Cardiac Markers in Patients with Acute Myocar dial Infarction: Oxidative Stress, C-Reactive Protein and N-Terminal Probrain Natriuretic Peptide. Journal of Clinical Biochemistry and Nutrition. 2007;41(1):50-7.
4. Tompkins AJ, Burwell LS, Digerness SB, Zaragoza C, Holman WL, Brookes PS. Mitochondrial dysfunction in cardiac ischemia-reperfusion injury: ROS from complex I, without inhibition. Biochimica et biophysica acta. 2006;1762(2):223-31.
5. Urso ML, Clarkson PM. Oxidative stress, exercise, and antioxidant supplementation. Toxicology. 2003;189(1-2):41-54.
6. Jolazadeh T, Dabidi Roshan V, S. M. Apoptosis in cardiac cells in response to acute exercise protocol: An experimental protocol in the sedentary rats. . Sport Sciences Research Institute of Iran. 2010;11:27-36.
7. Ranjbar K, Noorshahi M, Hedayati M, H. Tc. Evaluation of serum levels of angiogenic factors in response to a session of activity Submaximal prolonged sedentary men. Physio Pharm. 2011;15:124-32.
8. Ushio-Fukai M, Nakamura Y. Reactive oxygen species and angiogenesis: NADPH oxidase as target for cancer therapy. Cancer letters. 2008;266(1):37-52.
9. Taheri chadorneshin H, Noorshahi M RK. VEGF’s response to practice and its relation to VO2max. Life Sciences Sports. 2011;7:59-75.
10. Noorshahi M, Frahmand F, M. B. The effect of a cinnamon extract supplement on VEGF and endostatine response of endometrial muscle after one session of exhaustive activity in elderly rats. Phys Pharm. 2015(1):170-8.
11. Van Craenenbroeck EM, Vrints CJ, Haine SE, Vermeulen K, Goovaerts I, Van Tendeloo VF, et al. A maximal exercise bout increases the number of circulating CD34+/KDR+ endothelial progenitor cells in healthy subjects. Relation with lipid profile. Journal of applied physiology (Bethesda, Md : 1985). 2008;104(4):1006-13.
12. Dulak J, Jozkowicz A, Dembinska-Kiec A, Guevara I, Zdzienicka A, Zmudzinska-Grochot D, et al. Nitric oxide induces the synthesis of vascular endothelial growth factor by rat vascular smooth muscle cells. Arteriosclerosis, thrombosis, and vascular biology. 2000;20(3):659-66.
13. Lee HJ, Koh GY. Shear stress activates Tie2 receptor tyrosine kinase in human endothelial cells. Biochemical and biophysical research communications. 2003;304(2):399-404.
14. Iemitsu M, Maeda S, Jesmin S, Otsuki T, Miyauchi T. Exercise training improves aging-induced downregulation of VEGF angiogenic signaling cascade in hearts. American journal of physiology Heart and circulatory physiology. 2006;291(3):H1290-8.
15. Goto F, Goto K, Weindel K, Folkman J. Synergistic effects of vascular endothelial growth factor and basic fibroblast growth factor on the proliferation and cord formation of bovine capillary endothelial cells within collagen gels. Laboratory investigation; a journal of technical methods and pathology. 1993;69(5):508-17.
16. Kroon ME, Koolwijk P, van der Vecht B, van Hinsbergh VW. Hypoxia in combination with FGF-2 induces tube formation by human microvascular endothelial cells in a fibrin matrix: involvement of at least two signal transduction pathways. Journal of cell science. 2001;114(Pt 4):825-33.
17. Friehs I, Barillas R, Vasilyev NV, Roy N, McGowan FX, del Nido PJ. Vascular endothelial growth factor prevents apoptosis and preserves contractile function in hypertrophied infant heart. Circulation. 2006;114(1 Suppl):I290-5.
18. Rivilis I, Milkiewicz M, Boyd P, Goldstein J, Brown MD, Egginton S, et al. Differential involvement of MMP-2 and VEGF during muscle stretch- versus shear stress-induced angiogenesis. American journal of physiology Heart and circulatory physiology. 2002;283(4):H1430-8.
19. Kandasamy AD, Chow AK, Ali MA, Schulz R. Matrix metalloproteinase-2 and myocardial oxidative stress injury: beyond the matrix. Cardiovascular research. 2010;85(3):413-23.
20. Mohamad HE, Askar ME, Hafez MM. Management of cardiac fibrosis in diabetic rats; the role of peroxisome proliferator activated receptor gamma (PPAR-gamma) and calcium channel blockers (CCBs). Diabetology & metabolic syndrome. 2011;3(1):4.
21. Westermann D, Rutschow S, Jager S, Linderer A, Anker S, Riad A, et al. Contributions of inflammation and cardiac matrix metalloproteinase activity to cardiac failure in diabetic cardiomyopathy: the role of angiotensin type 1 receptor antagonism. Diabetes. 2007;56(3):641-6.
22. Kwak HB, Kim JH, Joshi K, Yeh A, Martinez DA, Lawler JM. Exercise training reduces fibrosis and matrix metalloproteinase dysregulation in the aging rat heart. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2011;25(3):1106-17.
23. Yung YC, Chae J, Buehler MJ, Hunter CP, Mooney DJ. Cyclic tensile strain triggers a sequence of autocrine and paracrine signaling to regulate angiogenic sprouting in human vascular cells. Proceedings of the National Academy of Sciences of the United States of America. 2009;106(36):15279-84.
24. Gustafsson T, Rundqvist H, Norrbom J, Rullman E, Jansson E, Sundberg CJ. The influence of physical training on the angiopoietin and VEGF-A systems in human skeletal muscle. Journal of applied physiology (Bethesda, Md : 1985). 2007;103(3):1012-20.
25. Lloyd PG, Prior BM, Yang HT, Terjung RL. Angiogenic growth factor expression in rat skeletal muscle in response to exercise training. American journal of physiology Heart and circulatory physiology. 2003;284(5):H1668-78.
26. Ding YH, Luan XD, Li J, Rafols JA, Guthinkonda M, Diaz FG, et al. Exercise-induced overexpression of angiogenic factors and reduction of ischemia/reperfusion injury in stroke. Current neurovascular research. 2004;1(5):411-20.
27. Nakamura K, Kitaoka K, Tomita K. Effect of eccentric exercise on the healing process of injured patellar tendon in rats. Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association. 2008;13(4):371-8.
28. Kang YJ. The Antioxidant Function of Metallothionein in the Heart. Proceedings of the Society for Experimental Biology and Medicine. 1999;222(3):263-73.
29. Giral P, Ratziu V, Couvert P, Carrie A, Kontush A, Girerd X, et al. Plasma bilirubin and gamma-glutamyltransferase activity are inversely related in dyslipidemic patients with metabolic syndrome: relevance to oxidative stress. Atherosclerosis. 2010;210(2):607-13.
30. Siu PM, Bryner RW, Martyn JK, Alway SE. Apoptotic adaptations from exercise training in skeletal and cardiac muscles. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2004;18(10):1150-2.
31. Zhao W, Zhao T, Chen Y, Ahokas RA, Sun Y. Reactive oxygen species promote angiogenesis in the infarcted rat heart. International Journal of Experimental Pathology. 2009;90(6):621-9.
32. Kilic M, Ulusoy O, Cirrik S, Hindistan IE, Ozkaya YG. Effect of exercise intensity on cerebrospinal fluid interleukin-6 concentration during recovery from exhaustive exercise in rats. Acta physiologica Hungarica. 2014;101(1):21-31.
33. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods (San Diego, Calif). 2001;25(4):402-8.
34. Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry. 1976;72(1):248-54.
35. Guevara I, Iwanejko J, Dembinska-Kiec A, Pankiewicz J, Wanat A, Anna P, et al. Determination of nitrite/nitrate in human biological material by the simple Griess reaction. Clinica chimica acta; international journal of clinical chemistry. 1998;274(2):177-88.
36. Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. The Journal of laboratory and clinical medicine. 1967;70(1):158-69.
37. Tang K, Xia FC, Wagner PD, Breen EC. Exercise-Induced VEGF Transcriptional Activation in Brain, Lung and Skeletal Muscle. Respiratory physiology & neurobiology. 2010;170(1):16-22.
38. Siafakas NM, Jordan M, Wagner H, Breen EC, Benoit H, Wagner PD. Diaphragmatic angiogenic growth factor mRNA responses to increased ventilation caused by hypoxia and hypercapnia. The European respiratory journal. 2001;17(4):681-7.
39. Loufrani L, Henrion D. Role of the cytoskeleton in flow (shear stress)-induced dilation and remodeling in resistance arteries. Medical & biological engineering & computing. 2008;46(5):451-60.
40. Gavin TP, Westerkamp LM, Zwetsloot KA. Soleus, plantaris and gastrocnemius VEGF mRNA responses to hypoxia and exercise are preserved in aged compared with young female C57BL/6 mice. Acta physiologica (Oxford, England). 2006;188(2):113-21.
41. Carmeliet P. Angiogenesis in health and disease. Nature medicine. 2003;9(6):653-60.
42. Nazem F, Hokkamian E, Ranjbar K, Nazari A. The Effects of Aerobic Training on Renal Oxidative Stress in Myocardial Infarction Rats. Sport Physiology. 2017;9(34):79-94.
43. Zolfeghar Didani H, Zolfeghar Didani MR, Asri Rezai S, Ghaderi Pakdel F. Effect of Short Term Nano Selenium Supplementation and Exhausted Training in Oxidation Indices on Heart Tissue of Male Rats. Sport Physiology. 2017;9(35):49-62.
  • تاریخ دریافت: 12 دی 1397
  • تاریخ بازنگری: 12 اسفند 1397
  • تاریخ پذیرش: 18 خرداد 1399
  • تاریخ اولین انتشار: 01 تیر 1400
  • تاریخ انتشار: 01 تیر 1400