Advances in Clinical and Experimental Medicine

Title abbreviation: Adv Clin Exp Med
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Advances in Clinical and Experimental Medicine

2017, vol. 26, nr 4, July, p. 595–599

doi: 10.17219/acem/62535

PubMed ID: 28691417

Publication type: original article

Language: English

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Effect of endovascular coronary low-level laser therapy during angioplasty on the release of endothelin-1 and nitric oxide

Arkadiusz Derkacz1,2,A,B,C,D,E,F, Alicja Szymczyszyn1,2,E, Ewa Szahidewicz-Krupska1,2,C,D, Marcin Protasiewicz2,3,A,B, Rafał Poręba1,C, Adrian Doroszko1,2,C,D,E,F

1 Department and Clinic of Internal and Occupational Disease, Hypertension and Clinical Oncology, Wroclaw Medical University, Poland

2 Wrovasc – Integrated Cardiovascular Centre Provincial Specialist Hospital in Wroclaw, Research and Development Department, Wrocław, Poland

3 Department of Cardiology, Wroclaw Medical University, Wrocław, Poland

Abstract

Background. Nitric oxide (NO) and endothelin-1 are potentially significant factors contributing to the pathogenesis of post-angioplasty restenosis. It may be postulated that low-level laser therapy (LLLT) can favorably influence the process of restenosis by affecting those factors.
Objectives. The aim of the study was to evaluate the effect of LLLT applied during percutaneous coronary intervention (PCI) on the factors participating in the homeostasis of vascular tone – NO and endothelin-1.
Material and Methods. In a randomized, prospective study of 52 subjects undergoing PCI, an additional 808 nm intravascular LLLT was applied at a dose of 9 J/cm2 in the lesion part. The control group was 49 subjects with PCI only. We assessed the concentration of nitrites/nitrates reflecting NO metabolism as well as endothelin-1 in both groups before PCI, and at 6 h, 12 h and 1 month after the procedure. In addition, half a year after PCI, a follow-up angiography was performed.
Results. Statistically higher nitrite/nitrate concentrations were observed in the laser group as compared to the control group in all tests except the pre-PCI assays. Endothelin-1 levels were significantly higher in the laser group 6 h after PCI with a significant decrease in subsequent tests, which was not observed in the control group. The restenosis rate was 15.0% in the laser group and 32.4% in the control group (however the difference was not statistically significant).
Conclusion. LLLT applied during the PCI procedure can influence the process of restenosis by modifying NO and endothelin-1 concentrations.

Key words

low-level laser therapy, coronary angioplasty, restenosis, nitric oxide, endothelin-1

References (24)

  1. Baek SH, Hrabie JA, Keefer LK, et al. Augmentation of intrapericardial nitric oxide level by a prolonged-release nitric oxide donor reduces luminal narrowing after porcine coronary angioplasty. Circulation. 2002;105:2779–2784.
  2. Torella D, Leosco D, Indolfi C, et al. Aging exacerbates negative remodeling and impairs endothelial regeneration after balloon injury. Am J Physiol Heart Circ Physiol. 2004;287:2850–2860.
  3. Kitada K, Yui N, Matsumoto C, Mori T, Matsumura Y. Inhibition of endothelin ETB receptor system aggravates neointimal hyperplasia after balloon injury of rat carotid artery. J Pharmacol Exp Ther. 2009;331:998–1004.
  4. Kirchengast M, Munter K. Endothelin and restenosis. Cardiovasc Res. 1998;39:550–555.
  5. Kaul U, Singh B, Sudan D, Ghose T, Kipshidze N. Intravascular red light therapy after coronary stenting – angiographic and clinical follow-up study in humans. J Invas Cardiol. 1998;10:534–538.
  6. De Scheerder IK, Wang K, Kaul U, et al. Intravascular low-power laser irradiation after coronary stenting: Long-term follow-up. Lasers Surg Med. 2001;28:212–215.
  7. Derkacz A, Protasiewicz M, Poreba R, Szuba A, Andrzejak R. Usefulness of intravascular low power laser illumination in preventing restenosis after percutaneous coronary intervention. Am J Cardiol. 2010;106:1113–1117.
  8. Chan A, Moliterno D. Restenosis: The clinical issues. In: Textbook of interventional cardiology. Eds.: Topol E, W. B. Saunders Company, Philadelphia, 2002, 4nd ed., 415–453.
  9. Pawlik E, Grobelny A, Pałasz Z, et al. Method of intravascular low power laser illumination. Opt Appl. 2001;31:761–767.
  10. Beres-Pawlik E, Derkacz A. Intravascular low-power laser illumination through special fiber diffusers. Bull Pol Ac Tech. 2011;59:441–443.
  11. Derkacz A, Protasiewicz M, Kipshidze N, et al. Endoluminal photo-therapy for prevention of restenosis. Preliminary result at 6-month follow-up. Photomed Laser Surg. 2005;23:536–542.
  12. Hoffmann R, Takimoglu-Boerekci M, Langenberg R, et al. Randomized comparison of direct stenting with predilatation followed by stenting on vessel trauma and restenosis. Am Heart J. 2004;147:E13.
  13. Liu N, Chen G, Wang X, et al. Effects of certain vasoactive peptides on pathogenesis of vascular restenosis. Chin Med Sci J. 2003;18:1–8.
  14. Avizohar O, Karnieli E, Shen-Orr ZA, Rappaport B, Beyar R. Plasma endothelin levels as a function of coronary artery manipulation during balloon angioplasty and high-speed rotational atherectomy. Int J Cardiovasc Intervent. 1998;1:93–98.
  15. Chaudhry H, Lynch M, Schomacker K, Birngruber R, Gregory K, Kochevar I. Relaxation of vascular smooth muscle induced by low-power laser radiation. Photochem Photobiol. 1993;58:661–669.
  16. Osipov, Borisenko G, Kazarinov K, Vladimirov I. Nitric oxide, hemoglobin and laser irradiation. Vestn Ross Akad Med Nauk. 2000;4:48–52.
  17. Vladimirov I, Klebanov G, Borisenko G, Osipov A. Molecular and cellular mechanisms of the low intensity laser radiation effect. Biofizika. 2004;49:339-350.
  18. Kipshidze N, Keelan MH, Petersen JR, et al. Photoactivation of vascular iNOS and elevation of cGMP in vivo: Possible mechanism for photovasorelaxation and inhibition of restenosis in an atherosclerotic rabbit models. Photochem Photobiol. 2000;72:579–582.
  19. Sluiter W, de Vree WJ, Pietersma A, Koster JF. Prevention of late lumen loss after coronary angioplasty by photodynamic therapy: Role of activated neutrophils. Mol Cell Biochem. 1996;157:233–238.
  20. Kipshidze N, Sahota H, Komorowski R, Nikolaychik V, Keelan MH. Photoremodeling of arterial wall reduces restenosis after balloon angioplasty in an atherosclerotic rabbit model. J Am Coll Cardiol. 1998;31:1152–1157.
  21. Kipshidze N, Keelan M, Nikolaychik V. Impact of red light on restenosis. In: Vascular Brachytherapy. Eds.: Waksman R, King S, Crocker I, Mould R, Nucleotron 1996:165–175.
  22. De Scheerder IK, Wang K, Zhou XR, et al. Intravascular low power red laser light as an adjunct to coronary stent implantation evaluated in a porcine coronary model. J Invas Cardiol. 1998;10:263–268.
  23. De Scheerder I, Wang K, Nikolaychik V, et al. Long-term follow-up after coronary stenting and intravascular red laser therapy. Am J Cardiol. 2000;86:927–930.
  24. Derkacz A, Protasiewicz M, Poręba R, Doroszko A, Andrzejak R. Effect of the intravascular low energy laser illumination during percutaneous coronary intervention on the inflammatory process in vascular wall. Lasers Med Sci. 2013;28:763–768.