Artigo Acesso aberto Revisado por pares

Laser Myocardial Revascularization Modulates Expression of Angiogenic, Neuronal, and Inflammatory Cytokines in a Porcine Model of Chronic Myocardial Ischemia

2010; Wiley; Volume: 17; Issue: 5 Linguagem: Inglês

10.1111/j.1540-8191.2001.tb01171.x

ISSN

1540-8191

Autores

Shmuel Fuchs, Richard Baffour, Yoram Vodovotz, Matie Shou, Eugenio Stabile, Fermin O. Tio, Martin B. Leon, Ran Kornowski,

Tópico(s)

Pain Management and Treatment

Resumo

Journal of Cardiac SurgeryVolume 17, Issue 5 p. 413-424 Laser Myocardial Revascularization Modulates Expression of Angiogenic, Neuronal, and Inflammatory Cytokines in a Porcine Model of Chronic Myocardial Ischemia Shmuel Fuchs M.D., Corresponding Author Shmuel Fuchs M.D. Washington Hospital Center, Washington, DCCardiovascular Research Institute, Washington Hospital Center, 110 Irving Street N.W., Suite 4B-1, Washington D.C. 20010. Fax: 202–877–2715; e-mail: [email protected]Search for more papers by this authorRichard Baffour Ph.D, Richard Baffour Ph.D Washington Hospital Center, Washington, DCSearch for more papers by this authorYoram Vodovotz Ph.D, Yoram Vodovotz Ph.D Washington Hospital Center, Washington, DCSearch for more papers by this authorMatie Shou M.D., Matie Shou M.D. Washington Hospital Center, Washington, DCSearch for more papers by this authorEugenio Stabile M.D., Eugenio Stabile M.D. Washington Hospital Center, Washington, DCSearch for more papers by this authorFermin O. Tio M.D.,, Fermin O. Tio M.D., Biomedical Research Foundation of South Texas, Inc., San Antonio, TexasSearch for more papers by this authorMartin B. Leon M.D.,, Martin B. Leon M.D., Lenox Hill Hospital, New York, New YorkSearch for more papers by this authorRan Kornowski M.D., Ran Kornowski M.D. Washington Hospital Center, Washington, DCSearch for more papers by this author Shmuel Fuchs M.D., Corresponding Author Shmuel Fuchs M.D. Washington Hospital Center, Washington, DCCardiovascular Research Institute, Washington Hospital Center, 110 Irving Street N.W., Suite 4B-1, Washington D.C. 20010. Fax: 202–877–2715; e-mail: [email protected]Search for more papers by this authorRichard Baffour Ph.D, Richard Baffour Ph.D Washington Hospital Center, Washington, DCSearch for more papers by this authorYoram Vodovotz Ph.D, Yoram Vodovotz Ph.D Washington Hospital Center, Washington, DCSearch for more papers by this authorMatie Shou M.D., Matie Shou M.D. Washington Hospital Center, Washington, DCSearch for more papers by this authorEugenio Stabile M.D., Eugenio Stabile M.D. Washington Hospital Center, Washington, DCSearch for more papers by this authorFermin O. Tio M.D.,, Fermin O. Tio M.D., Biomedical Research Foundation of South Texas, Inc., San Antonio, TexasSearch for more papers by this authorMartin B. Leon M.D.,, Martin B. Leon M.D., Lenox Hill Hospital, New York, New YorkSearch for more papers by this authorRan Kornowski M.D., Ran Kornowski M.D. Washington Hospital Center, Washington, DCSearch for more papers by this author First published: 12 July 2010 https://doi.org/10.1111/j.1540-8191.2001.tb01171.xCitations: 10AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Abstract Abstract Background: Controversy exists whether transmyocardial laser revascularization (TMR) is associated with angiogenesis or neuromodulation and whether these are time-dependent phenomena. Accordingly, we performed a time-course analysis of the expression of angiogenic and neuronal factors following experimental percutaneous TMR. Methods and Results: Five weeks after placing ameroid constrictors on the circumflex coronary artery, 16 pigs underwent left ventricular mapping guided TMR using Ho:YAG laser (2 J × 1 pulse) at 30 sites directed at the ischemic zones and 11 animals were ischemic controls. Histology and immunostaining were obtained at 1 and 2 weeks (4 TMR and 3 controls at each time point) and at 4 weeks (8 TMR and 5 controls) for vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), nerve growth factor (βNGF), substance P (SP), and monocyte chemoattractant protein-1 (MCP-1). Immunoreactivity was scored using a digital image analysis system. Factor VIII staining was used for blood vessel counting. Enhanced regional expression of VEGF, bFGF and MCP-1 in the TMR group was noted at 1 and 2 weeks with a threefold increase at 4 weeks following TMR compared to controls. βNGF expression in the TMR group was enhanced at 1 and 2 weeks with subsequent decline at 4 weeks to the controls level. SP expression was not significantly different between groups at all time points. There was a twofold increase in the number of blood vessels in the TMR group at 4 weeks, which was not apparent earlier. Conclusions: These immunohistological findings suggest that cytokines expression compatible with angiogenesis and neuromodulation occurs early after TMR. Up-regulation of angiogenic and inflammatory cytokines may be more sustained than neuromodulation. REFERENCES 1 Cooley DA, Frazier OH, Kadipasaoglu KA, et al: Transmyocardial laser revascularization: Clinical experience with twelve-month follow-up. J Thorac Cardiovasc Surg 1996; 111: 791– 799. 2 Horvath KA, Cohn LH, Cooley DA, et al: Transmyocardial laser revascularization results of a multicenter trial with transmyocardial laser revascularization used as sole therapy for end-stage coronary artery disease. J Thorac Cardiovasc Surg 1997; 113: 645– 654. 3 Milano A., Pratali S., Tartarini G., et al: Early results of transmyocardial revascularization with a Holmium laser. Ann Thorac Surg 1998; 65: 700– 704. 4 Burkhoff D., Schmidt S., Schulman SP, et al: Transmyocardial laser revascularisation compared with continued medical therapy for treatment of refractory angina pectoris: A prospective randomised trial. ATLANTIC Investigators. Angina Treatments-Lasers and Normal Therapies in Comparison. Lancet 1999; 354: 885– 890. 5 Allen KB, Dowling RD, Fudge TL, et al. Comparison of transmyocardial revascularization with medical therapy in patients with refractory angina. N Engl J Med 1999; 341: 1029– 1036. 6 Aaberge L., Nordstrand K., Dragsund M., et al: Transmyocardial revascularization with CO2 laser in patients with refractory angina pectoris. Clinical results from the Norwegian randomized trial. J Am Coll Cardiol 2000; 35: 1170– 1177. 7 Lauer B., Junghans U., Stahl F., et al: Catheter-based percutaneous myocardial laser revascularization in patients with end-stage coronary artery disease. J Am Coll Cardiol 1999; 34: 1663– 1670. 8 Lauer B., Stahl F., Junghans U., et al: Long-term results after percutaneous myocardial laser revascularization in patients with end stage coronary artery disease. (Abstract) J Am Coll Cardiol 1999; 23 (Suppl A): 381A. 9 Oesterle SN, Sanborn TA, Ali N., et al: Percutaneous transmyocardial laser revascularisation for severe angina: The PACIFIC randomised trial. Potential Class Improvement From Intramyocardial Channels. Lancet 2000; 356: 1705– 1710. 10 Kornowski R., Bairn DS, Moses JW, et al: Acute and intermediate-term clinical outcomes from direct myocardial laser revascularization guided by Biosense(tm) left ventricular electro-mechanical mapping. Circulation 2000; 102: 1120– 1125. 11 Schofield PM, Sharpies LD, Caine N., et al: Transmyocardial laser revascularisation in patients with refractory angina: A randomised controlled trial. Lancet 1999; 353: 519– 524. 12 Leon MB, Kornowski R., Bairn DS, et al: Direct myocardial laser revascularization using Biosense left ventricular electromechanical mapping: final results of the DIRECT randomized trial. Presented at the Am Coll Cardiol 50th Scientific Session, Orlando, FL, March 2001. 13 Kornowski R., Hong MK, Haudenschild C., et al: Feasibility and safety of percutaneous direct myocardial revascularization using Biosense(tm) system in porcine hearts. Coronary Artery Disease 1998; 9: 535– 540. 14 Yamamoto N., Kohmoto T., Gu A., et al: Angiogenesis is enhanced in ischemic canine myocardium by transmyocardial laser revascularization. J Am Coll Cardiol 1998; 31: 1426– 1433. 15 Kwong KF, Kanellopoulos GK, Nickols JC, et al: Transmyocardial laser denervates canine myocardium. J Thorac Cardiovasc Surg 1997; 114: 883– 889. 16 Ben-Haim SA, Osadchy D., Schuster I., et al: Non-fluoroscopic, in vivo navigation and mapping technology. Nature Med 1996; 2: 1393– 1395. 17 Gepstein L., Hayam G., Ben-Haim SA. A novel method for non-fluoroscopic catheter based electroanatomical mapping of the heart: in vitro and in vivo accuracy results. Circulation 1997; 95: 1611– 1622. 18 Kornowski R., Hong MK, Gepstein L., et al: Preliminary animal and clinical experiences using an electromechanical endocardial mapping procedure to distinguish infarcted from healthy myovardium. Circulation 1998; 98: 1116– 1124. 19 Fuchs S., Kornowski R., Shiran A., et al: Electromechanical characterization of myocardial hibernation in a pig model. Coronary Artery Disease 1999; 3: 195– 198. 20 Fuchs S., Baffour R., Shou M., et al: Transendocar-dial delivery of autologous bone marrow enhances collateral perfusion and regional function in pigs with chronic experimental myocardial ischemia. (Abstract) J Am Coll Cardiol 2000; 35(Suppl A): 60A. 21 Cercek B., Yamashita M., Dimayuga P., et al: Nuclear factor kB activity and arterial response to balloon injury. Atherosclerosis 1997; 13: 59– 66. 22 Roth DM, Maruoka Y., Rogers J., et al: Development of coronary collateral circulation in left circumflex ameroid-occluded swine myocardium. Am J Physiol 1987; 253: H1279– 1288. 23 Shen YT, Vatner SF. Mechanism of impaired myocardial function during progressive coronary stenosis in conscious pigs. Hibernation versus stunning? Circ Res 1995; 76: 479– 488. 24 Ito WD, Arras M., Winkler B., et al: Monocyte chemotactic protein-1 increases collateral and peripheral conductance after femoral artery occlusion. Circ Res 1997; 80: 829– 837. 25 Buschmann I., Schaper W.: The pathophysiology of the collateral circulation (arteriogenesis). J Pathol 2000; 190: 338– 342. 26 Chu V., Kuang JQ, McGinn A., et al: Angiogenic response induced by mechanical transmyocardial revascularization. J Thorac Cardiovasc Surg 1999; 118: 849– 856. 27 Horvath KA, Chiu E., Maun DC, et al: Up-regulation of vascular endothelial growth factor mRNA and angiogenesis after transmyocardial laser revascularization. Ann Thorac Surg 1999 68): 825– 829. 28 Fisher PE, Khomoto T., DeRosa CM, et al: Histologic analysis of transmyocardial channels: Comparison of CO2 and holmium: YAG lasers. Ann Thorac Surg 1997; 64: 466– 472. 29 Huang MH, Sylven C., Horackova M., et al: Ventricular sensory neurons in canine dorsal root ganglia: Effects of adenosin and substance P. Am J Physiol 1995; 269: R318– 324. 30 Raivich G., Kreutzberg GW: Nerve growth factor and regeneration of peripheral nervous system. Clin Neurol Neurosurg 1993; 95 Suppl: S84– 88. 31 Neumann R., Korsching S., Bandtlow C., et al: Changes of nerve growth factor synthesis in non-neuronal cells in response to sciatic nerve tran-section. J Cell Biol 1987; 104: 1623– 1631. 32 Gu Y., Yong Q., Yoshida K., et al: Rapid increase in NGF-1 mRNA after ischemia/reperfusion and preconditioning in rat heart. (Abstract) Circulation 1994;(Suppl I): I– 249. 33 Abe T., Morgan D., Gutterman DD: Protective role of nerve growth factor against postischemic dysfunction of sympathetic coronary innervation. Circulation 1997; 95: 213– 220. 34 Kaye MP, Wells DJ, Tyce GM.: Nerve growth factor-enhanced reinnervation of surgically denervated canine heart. Am J Physiol 1979; 236: H624– 628. 35 Lindholm D., Heumann R., Meyer M., et al: Interleukin-1 regulates synthesis of nerve growth factor in non-neuronal cells of rat sciatic nerve. Nature 1987; 330: 658– 659. 36 Hirsch GM, Thompson GW, Arora RC, et al: Trans-myocardial laser revascularization does not denervate the canine heart. Ann Thorac Surg 1999; 68: 460– 468. 37 Al-Sheikh T., Allen KB, Straka SP, et al: Cardiac sympathetic denervation after transmyocardial laser revascularization. Circulation 1999; 100: 135– 140. 38 Kwong KF, Schuessler RB, Kanellopoulos GK, et al: Nontransmural laser treatment incompletely denervates canine myocardium. Circulation 1998; 98(19 Suppl): II67– 71. 39 Wang DL, Wung BS, Shyy YJ, et al: Mechanical strain induces monocyte chemotactic protein-1 gene expression in endothelial cells. Effects of me chanical strain on monocyte adhesion to endothelial cells. Circ Res 1995; 77: 294– 302. 40 Wemper F., Lindner V., Augustin HG. Basic fibroblast growth factor (bFGF) regulates the expression of the CC chemokine monocyte chemoattractant protein-1 (MCP-1) in autocrine-activated endothelial cells. Arterioscler Thromb Vase Biol 1997; 17: 2471– 2478. 41 Marumo T., Schini-Kerth VB, Busse R. Vascular endothelial growth factor activates nuclear factor-kappaB and induces monocyte chemoattractant protein-1 in bovine retinal endothelial cells. Diabetes 1999; 48: 1131– 1137. 42 Byrd VM, Ballard DW, Miller GG, et al: Fibroblast growth factor-1 (FGF-1) enhances IL-2 production and nuclear translocation of NF-kappaB in FGF receptor-bearing Jurkat T cells. J Immunol 1999; 162: 5853– 5859. 43 Horvath KA, Smith WJ, Laurence RG, et al: Recovery and viability of an acute myocardial infarct after transmyocardial laser revascularization. J Am Coll Cardiol 1995; 25: 258– 263. 44 Mack CA, Magovern CJ, Hahn RT, et al: Channel patency and neovascularization after t transmyocardial revascularization using an excimer laser: Results and comparison to nonlased channels. Circulation 1996;(Suppl. II): II-65– II-69. 45 Kohmoto T., Fisher PE, Gu A., et al: Does blood flow through Holmium: YAG transmyocardial laser channels? Ann Thorac Surg 1996; 61: 861– 868. 46 Horvath KA, Chiu E., Maun DC, et al: Up-regulation of vascular endothelial growth factor mRNA and angiogenesis after transmyocardial laser revascularization. Ann Thorac Surg 1999; 68: 825– 829. Citing Literature Volume17, Issue5September 2001Pages 413-424 ReferencesRelatedInformation

Referência(s)